Absolute Antibody was founded in 2012 with a vision to make engineered recombinant antibodies accessible to all, and we remain the only company 100% focused on recombinant antibody technology. Though recombinant antibodies are standard in the pharmaceutical industry, these antibodies have not been as widely available for diagnostics or research. This is starting to change, however, due to the many advantages recombinant antibodies offer over traditional hybridoma-produced monoclonal antibodies.
Absolute Antibody has been at the forefront of the movement to make recombinant antibodies more readily available to all. In 2015, we were recognized in a Nature paper on the need to standardize research antibodies, and in 2018, we co-authored a mAbs Journal paper further illustrating the importance of using recombinant antibodies. Over the years, we have grown rapidly as demand for recombinant antibodies increases.
We specialize in antibody sequencing, engineering and recombinant expression, offering royalty-free custom services and a unique reagents catalog of engineered recombinant antibodies and Fc Fusion proteins. Our customers include leading pharmaceutical, biotechnology and diagnostics companies, as well as academic researchers worldwide; we have customers in 65 different countries and have sold to 14 of the top 15 pharmaceutical companies by revenue. This international customer base is served by our ISO 9001:2015-certified manufacturing facility in Northeast England and additional offices in Boston in the United States and Amsterdam in the Netherlands.
The Absolute Antibody team has deep experience in the therapeutic antibody and recombinant technology fields. Together, we have the knowledge and expertise to deliver high-quality products and services, as well as offer high-level consultation on our customers’ antibody development projects. Since our founding, we have produced more than 180 different antibody formats for our customers, as well as developed a reagents catalog of more than 13,000 engineered recombinant antibodies. For an example, check out one catalog clone (anti-EGFR, or Cetuximab) available in more than 30 different off-the-shelf formats.
In 2020, we received a Queen’s Award for Enterprise in International Trade for our rapid international expansion. To date, we have sequenced more than 5,000 hybridomas, completed more than 125 successful antibody humanization projects, and manufactured more than 21,000 different antibodies, making 865 grams of protein in total. We look forward to continuing this growth and working toward our vision of Engineered Recombinant Antibodies for All.
The vast majority of reagent monoclonal antibodies are generated from hybridomas, immortal antibody-producing cells created by fusing a tumor (myeloma) cell with an antibody-producing B cell from an immunized animal. However, hybridomas suffer from many limitations. They can undergo genetic drift, leading to batch-to-batch variability; they can be genetically unstable and stop expressing the antibody; and more than 30% of hybridomas contain additional antibody genes, meaning they are not actually monoclonal.
In contrast, recombinant antibodies are manufactured using synthetic genes expressed in a defined in vitro cell line. They offer a variety of benefits compared to traditional hybridoma-produced antibodies.
Looking to learn more about the benefits of recombinant antibodies? We answer the question “Why Go Recombinant?” in the below presentation, explaining how engineered recombinant antibodies allow researchers to improve experimental design and develop complex controls with absolute precision.
Absolute Antibody specializes in antibody sequencing, engineering and recombinant expression, producing an ever-increasing number of engineered recombinant antibodies at our ISO-certified antibody manufacturing facility. We’ve used our custom-built technology platform to develop a unique recombinant reagents catalog and provide antibody services to customers worldwide, demonstrating we have the technology, expertise and capacity to meet the growing demand for recombinant antibody technology.
Our HEXpress™ antibody expression platform rapidly produces high-quality antibodies at milligram-to-gram scale. This custom-built production platform includes our proprietary vectors, cloning system, and high-yielding mammalian cell lines. We use serum-free transient expression as a faster, more affordable alternative to stable CHO cell line generation, and can scale up to multi-gram quantities in a matter of weeks.
Our production platform can manufacture recombinant antibodies in any species, isotype or format, including multispecifics and fragments, with high purity and low endotoxin levels. This platform has enabled us to produce more than 21,000 different recombinant antibodies, making 865 grams of protein in total. In addition, we’ve used the platform to build our own catalog of more than 13,000 antibodies in recombinant engineered formats. For example, check out one catalog clone (anti-EGFR, or Cetuximab) available in more than 30 different off-the-shelf formats.
We’ve continued to increase our antibody production capacity in recent years, developing custom high-throughput purification robots as well as implementing a third production line that can recombinantly manufacture hundreds of different antibodies per week. To learn more about the development of our production platform, view a presentation from our CSO describing how we have scaled and optimized our antibody expression and purification systems.
We have developed a proprietary cloning system to enable rapid reformatting of antibodies into almost any format. This allows antibody engineering such as species, isotype or subtype switching; bispecific or trispecific antibodies; antibody fragments; chimerization and humanization; engineered Fc domains; and Fc fusion proteins. Learn more about our engineering services here, or view the 180+ different formats we have created here.
In addition, we don’t just produce existing antibody formats; we create and offer novel antibody engineering technologies to our customers. Our own novel technologies include:
If you want to learn more about the development of our recombinant antibody technology platform, check out our History of Innovation timeline below
We’ve developed a cutting-edge high-throughput (NGS) approach to hybridoma sequencing that delivers all variable domains present within a hybridoma, as well as a full analysis characterizing the hybridoma’s sequences and any heterogeneity present. The technology works on any species or isotype, and can rescue contaminated or non-viable cells.
Hybridoma sequencing protects valuable antibodies against contamination, genetic drift, accidental loss, and other unforeseen circumstances, securing customers’ antibody supply chains long-term. We have a large capacity and high success rate: we have sequenced more than 5,000 hybridomas. We also offer customers antibody protein sequencing when the hybridoma is unavailable, as well as a pioneering polyclonal sequencing service.
At Absolute Antibody, we have experience producing antibodies in a wide range of formats. Using our proprietary cloning system, we have manufactured more than 180 different antibody formats for customers around the world. We provide both custom antibody engineering services as well as a rapidly growing catalog of engineered recombinant antibodies.
Our Periodic Table of Antibodies represents most of the formats we have created to date. Explore our interactive Periodic Table of Antibodies
You can also follow the links below to learn more about some of the key formats:
Absolute Antibody’s recombinant antibody technology allows us to convert any antibody into a fragment, including single chain Fv (scFv), Fab or Fab2 formats. Antibody fragments offer an ideal alternative to full-length antibodies in certain situations, as they enable better tissue penetration, reduce non-specific binding, and increase antibody stability and solubility. Antibody fragments can also improve localization in super-resolution methods, or reduce false positives in sandwich ELISA-type diagnostic tests.
Our recombinant antibody catalog includes popular clones engineered into various fragment formats, while our custom engineering service enables the creation of fragments from any existing antibody. Contact us to discuss your project!
Below, we provide some additional details on our approach to the Fab2 format.
Fab2 antibody fragments are used in many applications or assays where the presence of the Fc region may cause problems. They are traditionally made by enzymatic cleavage of full-length antibodies, but this causes a range of contaminants as by-products and the resulting fragment is comparatively unstable.
At Absolute Antibody, we produce Fab2 antibodies recombinantly. Our recombinant version, called the AbFab2™ fragment, has a proprietary dimerization motif in place of the hinge region, which improves stability of the fragment. Contaminating fragments are not generated, and a His tag is added for purification. As with all recombinant antibodies, the fragments are chemically defined with high purity and ensured batch-to-batch reproducibility.
See the figure below to compare the standard industry approach to the Absolute Antibody approach. In addition, the below ELISA data demonstrates that our Fab2 antibodies have nearly identical behavior to the original IgG antibodies.
Chimeric antibodies consist of an antibody’s original antigen-binding variable domains with the constant domains from a different species. At Absolute Antibody, we offer an antibody chimerization service for almost any mammalian species, in particular human, mouse, rat, rabbit and hamster IgG with other species and isotypes available on request.
Chimeric antibodies retain the original antibody’s antigen specificity and affinity and are valuable tools for in vivo and in vitro research, as well as diagnostic assay development.
Interested in chimeric antibodies? Our recombinant antibody catalog includes products in a wide range of species, or we can convert any antibody into any species upon request – contact us to get started!
Antibodies of IgG isotype are the most commonly used antibodies in research, diagnostics and therapy. Upon hearing the word antibody, most of us will instantly think of those Y-shaped depictions of antibody-proteins meant to reflect the shape of IgG.
Yet nature offers a range of other formats with unique characteristics, which our recombinant antibody technology allows researchers to explore. Switching an antibody’s isotype or subtype might enable you to tailor effector function, reduce the number of needed controls, or open up new areas of investigation in allergy or autoimmunity research.
In addition to all IgG subtypes, we offer antibodies in the following isotypes:
Learn more about antibody isotypes and subtypes in our Antibody Resource, a free online reference resource for researchers.
Interested in a non-IgG antibody? In our recombinant antibody catalog, you can find clones engineered into different isotypes and subtypes, available for purchase off-the-shelf. We can also convert any antibody into any isotype or subtype upon request – contact us to get started!
Fc Silent™ represents a genetically engineered Fc domain developed at Absolute Antibody for research and assay development. It contains key point mutations that abrogate binding of Fc receptors (FcγR, FcR), abolishing antibody directed cytotoxicity (ADCC) effector function.
Our Fc Silent™ antibodies therefore enable researchers to remove effector function in vivo and reduce non-specific background in staining methods. In vivo, the antibodies benefit from the long plasma half-life (t1/2) associated with the Fc domain, with none of the cytolytic immune effector mechanisms associated with the wild-type Fc domain. In vitro, the antibodies can be used for flow cytometry and immunohistochemistry (IHC) applications to reduce non-specific background signal resulting from Fc receptor binding. The Fc Silent™ mutations do not affect other properties of the antibody, including their compatibility with secondary antibodies.
All Absolute Antibody antibodies and fusion proteins are available with the Fc Silent™ domain. Our reagents catalog includes species-specific Fc Silent™ domains, such as human, mouse, rabbit, rat and hamster, in stock and ready to purchase. If you don’t see your antibody of choice in the Fc Silent™ format, contact us – we’d be happy to produce it for you!
Mouse IgG2a and rat IgG2b isotypes are known to bind strongly to Fc receptors irrespective of the test antibody specificity. Isotype controls are employed to allow the researcher to distinguish between specific and non-specific background signals. In Figure 1, we show how murine macrophages are labelled almost as strongly by a rat IgG2b isotype control as by an anti-F4/80. Switching to Fc Silent™ antibodies results in reliable data with background staining indistinguishable from a secondary-antibody-only control. This also shows that Fc Silent™ antibodies are compatible with standard secondary antibodies.
Figure 2 uses surface plasmon resonance (SPR) and direct competitive inhibition ELISA to show that the Fc Silent™ format does not interact with murine or human Fc receptors. This data was provided by Dr. Stephen Beers at the University of Southampton.
Figure 2A and B. Sensogram showing binding of mouse wild-type and Fc Silent™ anti-F4/80 IgG2a monoclonal antibodies (Ab00106-2.0 and Ab00106-2.3, respectively) to immobilized mouse low and high affinity Fcγ receptors (CD16, CD16-2, CD32, CD64). Biacore SPR binding analysis shows that the Fc Silent™ antibody has lost its capacity to interact with the mouse Fc receptors.
Figure 2C and D. Sensogram showing binding of rat wild-type and Fc Silent™ anti-F4/80 monoclonal antibodies (Ab00106-8.1 and Ab00106-8.4, respectively) to immobilized mouse low and high affinity Fcγ receptors (CD16, CD16-2, CD32, CD64). Biacore SPR binding analysis shows that the Fc Silent™ antibody has lost its capacity to interact with the mouse Fc receptors.
Figure 2E. Direct competitive inhibition ELISA. 2µg/ml/well of human recombinant FcγR1 receptor (rCD64) was absorbed onto a 96-well plate. 40µg/ml biotinylated Alemtuzumab (Campath) was premixed with un-labelled serially diluted murine wild-type or Fc Silent™ anti-F4/80 [CI:A3-1] IgG2a monoclonal antibodies (Ab00106-2.0 or Ab00106-2.3, respectively) or Alemtuzumab (Campath; positive control). The data clearly show that the Fc Silent™ antibody, Ab00106-2.3, does not bind to the human Fc receptor.
Fc-mediated immune effector functions are an important part of an antibody’s natural function, but in many therapeutic antibodies, these interactions are not desirable and can lead to catastrophic side effects. Many approaches to eliminate effector function have been developed, but none completely silence the unwanted binding to Fc gamma receptors, except for one. The STR Fc silencing platform, developed by mAbsolve and former Absolute Antibody scientists, delivers the only truly silent Fc mutations described to date. The technology therefore has the potential to improve the safety and efficacy of therapeutic antibodies and Fc fusion proteins.
Additional information available in the PLOS One research article “Fc-engineered antibodies with immune effector functions completely abolished.”
Benefits of producing STR-modified recombinant antibodies with Absolute Antibody
Off-the-shelf STR silenced antibodies
Polyclonal antibodies and hybridoma-derived antibodies are made using animals. While this practice has brought us many great reagents and enabled important discoveries, many scientists are uneasy with the use of animals for the creation of their tools. Moreover, many funding bodies are pushing toward the use of reagents made without the use of animals or animal-derived components (e.g. serum).
As a result, the animal-free antibody movement has been gaining more and more traction in recent years, as supported by a recent letter on animal-free antibody alternatives published in Nature Biotechnology. Since our founding in 2012, Absolute Antibody has been at the forefront of making animal-free recombinant antibodies more readily available for research and diagnostic applications. We are now active members of committees to promote the use of animal-free recombinant antibodies, such as the US National Institutes of Health’s Interagency Coordinating Committee on the Validation of Alternative Methods.
The recombinant production platform we use at Absolute Antibody is completely animal and animal-component free. The platform is based on transient, chemical transfection of a HEK293 cell line cultured in a precisely defined, serum-free medium. We do not use viral transfection approaches. This process is used for both our custom antibody expression service, as well as to produce all the reagents in our rapidly growing catalog of recombinant antibodies and proteins.
Our reagents portfolio contains antibodies from diverse sources, including classic hybridomas which have been sequenced for re-creation via recombinant production. This means that while the reagent was originally discovered by immunizing an animal, the products available for purchase are completely animal-free. Other sources of antibodies include human B-cell sequencing, as well as antibodies discovered by phage display.
also support the sequencing of existing hybridoma and ascites-derived antibodies to enable animal-free recombinant production. We provide high-throughput (NGS) hybridoma sequencing and antibody protein sequencing services to customers worldwide. To learn more about sequencing existing antibodies, view our presentation, given as part of a webinar series organized by the US National Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM), the PETA International Science Consortium Ltd., and the European Union Reference Laboratory for alternatives to animal testing (EURL ECVAM).
If you want or need antibodies or proteins that have been made without animals or animal-derived components, you can be assured that every product available from Absolute Antibody will suit your requirements.
Antibodies form a powerful tool used by the immune system to protect us from various pathogens. However, antibodies can also have deleterious effects, as very widely demonstrated by type I hypersensitivity reactions, in particular what we commonly refer to as “allergies”.
Be it to pollen, bee stings or various foods – allergies are extremely common, with various theories as to why they appear to be on the increase.
To cater to researchers investigating allergies, we offer a range of antibodies against common allergens. Many of these antibodies have been shown to compete with naturally occurring IgE – the principal antibody isotype mediating allergies. We offer these antibodies as human IgE (along with antibodies against IgE itself) for use as calibrators and positive controls.
Antibody Name [Clone] | Expected Species Reactivity | Applications |
Anti-Almond Allergen [X151] | Almond), Prunus dulcis (Amygdalus dulcis | ELISA |
Anti-Almond Allergen [X50] | Almond), Prunus dulcis (Amygdalus dulci | ELISA |
Anti-Amphibian Allergen [X359] | Amphibia | ELISA |
Anti-Api m 2 [21E11] | Honeybee (Apis mellifera) | crystallization, ELISA |
Anti-Ara h 2 [PA12P3D08] | Peanut (Arachis hypogaea) | biolayer interferometry, ELISA |
Anti-Ara h 2/Ara h 3 [PA12P3F10] | Peanut (Arachis hypogaea) | biolayer interferometry, ELISA |
Anti-Asp f 1 [14H4] | Aspergillus fumigatus (Neosartorya fumigata) | IP, WB, ELISA |
Anti-Asp f 1 [17A5] | Aspergillus fumigatus (Neosartorya fumigata) | IP, WB, ELISA |
Anti-Asp f 1 [4F8] | Aspergillus fumigatus (Neosartorya fumigata) | IP, WB, ELISA |
Anti-Asp f9 [5C6] | Aspergillus fumigatus (Neosartorya fumigata) | IP, WB, ELISA |
Anti-Bet v 1 [BAB2] | Activate, WB, ELISA | Activate, WB, ELISA |
Anti-Bet v 1 [BAB3] | Birch (Betula pendula) | WB, ELISA |
Anti-Bet v 1 [BAB4] | Birch (Betula pendula) | WB, ELISA |
Anti-Bet v 1 [BAB5] | Birch (Betula pendula) | WB, ELISA |
Anti-Bet v 1 [BV16] | Birch (Betula pendula) | crystallography, WB, ELISA |
Anti-Bet v 1 [M0418] | Birch (Betula pendula) | crystallography, ELISA |
Anti-Bla g 1 [Bla g 1-scFv] | German Cockroach (B. germanica) | crystallography, ELISA |
Anti-Bla g 2 [4C3] | German Cockroach (B. germanica) | crystallography, ELISA |
Anti-Bla g 2 [7C11] | German Cockroach (B. germanica) | crystallography, ELISA |
Anti-Bos d 5 [D1] | Cow (Bos taurus) | crystallization |
Anti-C3a Receptor [D098G01] | Human | |
Anti-C3a Receptor [D1858G07] | Human | |
Anti-Cashew Allergen [X467] | Anacardium occidentale (Cashew) | ELISA |
Anti-Celery Allergen [X474] | Apium graveolens (Celery) | ELISA |
Anti-Coconut Allergen [X423] | Cocos nucifera (Coconut) | ELISA |
Anti-Der f 1 [6A8] | Dust Mite (Dermatophagoides farinae) | crystallization, ELISA |
Anti-Der p 1 [10B9] | Dust Mite (Dermatophagoides farinae) | crystallization, ELISA |
Anti-Der p 1 [5H8] | Dust Mite (Dermatophagoides farinae) | crystallization, ELISA |
Anti-Der p 1, Der f 1 [4C1] | House Dust Mite | ELISA |
Anti-Der p 2 [H10] | Dermatophagoides pteronyssinus | chimera studies, SPR |
Anti-Der p 2 [H5] | Dermatophagoides pteronyssinus | chimera studies, SPR |
Anti-Der p 7 [WH9] | House Dust Mite | Block, ELISA |
Anti-Fc epsilon R [IB10] | Human | Block, FC |
Anti-Fc epsilon R [IE7] | Human | FC |
Anti-FceR1 alpha [Mar-1] | Mouse | deplete, IP, FC, IHC |
Anti-Fel d 1 [REGN1909] | Cat (Felis catus) | crystallization, functional assay, SPR, Block, ELISA |
Anti-Gliadin [1E01] | barley, rye, spelt, triticale, Wheat | AlphaLISA, ELISA, FC |
Anti-Gliadin [1E03] | barley, rye, spelt, triticale, Wheat | AlphaLISA, ELISA, FC |
Anti-Gliadin [PEE14C7] | barley, rye, spelt, triticale, Wheat | ELISA |
Anti-Gliadin [VHH26] | barley, rye, spelt, triticale, Wheat | ELISA |
Anti-Hev b 6.02 [G7] | Para rubber tree (Hevea brasiliensis) | ELISA |
Anti-Hev b 6.02 [H8] | Para rubber tree (Hevea brasiliensis) | ELISA |
Anti-Hev b 6.02 [M8] | Para rubber tree (Hevea brasiliensis) | ELISA |
Anti-Homer1 [HC89] | Mouse | WB, ELISA, IF, IHC |
Anti-Homer1 [HS22] | Mouse | WB, ELISA, IF, IHC |
Anti-Homer1 [HS38] | Mouse | WB, ELISA, IF, IHC |
Anti-Homer1 [HS63] | Mouse | WB, ELISA, IF, IHC |
Anti-IDO1 [19C5] | Human | ELISA, IHC |
Anti-IgE [D9#3116] | Dog | WB, ELISA |
Anti-IgE [huMaE11 (Omalizumab)] | Human | crystallization, Block, ELISA |
Anti-IgE [mAbA9] | Mouse | Blocking, ELISA, FC |
Anti-IgE [TES-C21] | Human | Block, ELISA |
Anti-IL-12p40 [Antibody 80] | Human | functional assay, inhibit, neutralize, therapeutic, ELISA |
Anti-IL-1B [IC8] | Human | neutralize |
Anti-IL-1B [MAb201] | Human | ICC, inhibit, neutralize, WB |
Anti-IL-33 [309h] | Human | functional assay, inhibit, Block, ELISA |
Anti-IL-33 [874F7-Hu1] | Human, Cynomolgus Monkey, Mouse | functional assay, inhibit, neutralize, Block, ELISA |
Anti-IL-33 [H02-8F11Hz01] | Human, Cynomolgus Monkey, Mouse | functional assay, inhibit, Block, ELISA |
Anti-IL-33 [W3759-cAb1] | Human | ELISA |
Anti-IL-9 [MH9A4] | Human | ELISA, FC |
Anti-Lupin Allergen [X291] | Lupinus | ELISA |
Anti-Lysozyme [cAb-Lys3] | Chicken, hen, turkey | ELISA |
Anti-Lysozyme [D11.15] | black-necked pheasant, Chicken, helmeted guineafowl, Japanese quail | SPR, ELISA |
Anti-Macadamia Allergen [X313] | Macadamia nut | ELISA |
Anti-Pancreatic alpha-amylase [AMD9] | Pig (Sus scrofa) | ELISA |
Anti-Peanut Allergen [X378] | Arachis hypogaea | ELISA |
Anti-Phl p 1 [Clone 10] | Timothy-Grass (Phleum pratense) | WB |
Anti-Phl p 1 [Clone 25] | Timothy-Grass (Phleum pratense) | dotblot, WB, ELISA |
Anti-Phl p 1 [Clone 43] | Timothy-Grass (Phleum pratense) | WB |
Anti-Phl p 1 [p1-20] | Phleum pratense (common timothy) | ELISA |
Anti-Phl p 11 [p11-5] | Phleum pratense (common timothy) | ELISA |
Anti-Phl p 2 [p2-2] | Phleum pratense (common timothy) | ELISA |
Anti-Phl p 4 [p4-5] | Phleum pratense (common timothy) | ELISA |
Anti-Phl p 5 [4.2] | Timothy-Grass (Phleum pratense) | ELISA |
Anti-Phl p 5 [p5-11] | Phleum pratense (common timothy) | ELISA |
Anti-Phl p 6 [p6-1] | Phleum pratense (common timothy) | ELISA |
Anti-Soy Allergen [X259] | Glycine max (Glycine hispida, Soybean) | ELISA |
Coronaviruses are a group of viruses at the source of several recent outbreaks, including SARS (Severe Acute Respiratory Syndrome) in 2003, MERS (Middle East Respiratory Syndrome) in 2012 and most recently the outbreak of COVID-19, the illness caused by the SARS-CoV-2 virus. Our collection of anti-coronavirus antibodies was largely obtained from B-cell sequencing of human patients. In addition to the original human IgG1 antibodies, recombinant antibody technology has enabled the production of various engineered formats designed to open up new experimental possibilities for in vitro and in vivo use.
This year, the anti-SARS clone CR3022 was shown to have high affinity for the then-termed 2019-nCoV. The clone is now available in our catalog in formats such as IgM, IgA, antibody fragments, and IgG in different species and isotypes.
The Absolute Antibody team is working hard to support coronavirus research and therapeutic development by supplying related reagents to customers worldwide, as well as providing antibody engineering and manufacturing services. We continue to add new reagents to our catalog, including recombinant anti-human immunoglobulin antibodies for COVID-19 diagnostics and ACE2 Fc fusion proteins.
Clone Name | Available Formats | Applications |
Anti-Spike Protein [CV1] | Human IgG1, IgM, IgA, IgA1, IgA2, IgG2, IgG3, Fab fragment and Fab 2; Mouse IgG1, IgM, Fab fragment and Fab2; Rabbit IgG; Cat IgG1 and IgM; Ferret IgG1, IgM and IgA | NTRL, ELISA, FC, Therapeutic |
Anti-Spike Protein (RBD) [CV30] | Human IgG1, IgM, IgA, IgA1, IgA2, IgG2, IgG3, Fab fragment and Fab 2; Mouse IgG1, IgM, Fab fragment and Fab2; Rabbit IgG; Cat IgG1 and IgM; Ferret IgG1, IgM and IgA | NTRL, ELISA, FC, Therapeutic |
Anti-COVID-19 & SARS-CoV S glycoprotein [CR3022] | Human IgG1, IgM, IgG3, IgA, IgA1, Fab, Fab2, IgG2, IgG4 and IgE; Mouse IgG2b, IgM, Fab fragment and Fab2; Rabbit IgG; Cat IgM and IgG1; Ferret IgG1, IgM and IgA | NTRL, ELISA |
Anti-Covid-19 & SARS-CoV Nucleoprotein [CR3018 (03-018)] | Human IgG1, IgM, IgG3, IgA, IgA1, IgGA2, Fab, Fab2 and IgG2; Mouse IgG2b, IgM, Fab fragment and Fab2; Rabbit IgG; Cat IgM and IgG1; Ferret IgG1, IgM and IgA | ELISA, IF |
Anti-Covid-19 & SARS-CoV Nucleoprotein [CR3009 (03-009)] | Human IgG1, IgM, IgG3, IgA, IgA1, IgA2, Fab, Fab2 and IgG2; Mouse IgG2b, IgM, Fab fragment and Fab2; Rabbit IgG; Cat IgM and IgG1; Ferret IgG1, IgM and IgA | ELISA, IF |
Anti-Spike protein (RBD) [Sb#14]] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | ELISA, Blocking |
Anti-Spike protein (RBD) [Sb#15] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | ELISA, Blocking |
Anti-Spike protein (RBD) [Sb#16] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | ELISA, Blocking |
Anti-Spike protein (RBD) [Sb#42] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | ELISA, Blocking |
Anti-Spike protein (RBD) [Sb#45] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | ELISA, Blocking |
Anti-Spike protein (RBD) [Sb#68] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | ELISA, Blocking |
Anti-SARS-CoV S glycoprotein [S227] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S230] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S215] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S109] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S124] | Human IgG1, IgM, IgG3, IgA1, Fab fragment and Fab2; Mouse IgG2b; Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S222] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S231] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S228] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S226] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S217] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S223] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S110] | Human IgG1, IgM, IgG3, IgA1, Fab fragment and Fab2; Mouse IgG2b; Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [S225] | Human IgG1, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [4G2] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [5D3] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [6B1] | Human IgG, Human IgG2, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [5E4] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [1B5] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [4D4] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [11A] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [256] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA |
Anti-SARS-CoV S glycoprotein [A11] | Human IgG1, Human IgM, Mouse IgG, Mouse IgG2b, Mouse IgM, Rabbit IgG, scFv fragment | ELISA, IF, WB |
Anti-SARS-CoV S glycoprotein [F26G9] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA, IF |
Anti-SARS-CoV S glycoprotein [F26G10] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA, IF |
Anti-SARS-CoV S glycoprotein [F26G19] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL, ELISA, IF, WB |
Anti-MERS-CoV Spike Protein [D12] | Mouse IgG1, Rabbit IgG1 | NTRL, ELISA, IF |
Anti-MERS-CoV Spike Protein [4c2] | Mouse IgG1, Rabbit IgG1 | NTRL, ELISA |
Anti-MERS-CoV Spike Protein [3B12] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL |
Anti-MERS-CoV Spike Protein [M14D3] | Human IgG1, Human IgM, Mouse IgG1, Mouse IgM, Mouse IgG2b, Rabbit IgG | NTRL |
Anti-MERS-CoV Spike Protein [1F8] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL |
Anti-MERS-CoV Spike Protein [3A1] | Human IgG, Human IgM, Mouse IgG, Mouse IgM, Rabbit IgG | NTRL |
Anti-Bovine coronavirus [SF-3E4] | Mouse IgG1, Rabbit IgG1 | NTRL, ELISA, WB |
Anti-SARS-CoV-2 and SARS-CoV nucleocapsid [mBG17] | Human IgG1, IgG2, IgG3, IgE, IgM, IgA1, Fab fragment and Fab2; Mouse IgG1, IgG2b, IgM, Fab fragment and Fab2; Rabbit IgG; Ferret IgG1, IgM and IgA; Cat IgG1 and IgM | WB, ELISA, IF |
Anti-SARS-CoV-2 nucleocapsid [mBG86] | Human IgG1, IgG2, IgG3, IgM, IgA1, Fab fragment and Fab2; Mouse IgG1, IgA, IgM, IgG2b, Fab fragment and Fab2; Rabbit IgG; Ferret IgG1, IgM and IgA; Cat IgG1 and IgM | WB, ELISA, IF |
Anti-Spike protein [EY6A] | Human IgG1, IgG2, IgA1, IgM, Fab fragment and Fab2; Mouse IgG2b and IgM; Rabbit IgG | NTRL, Surface Plasmon Resonance, therapeutic, ELISA, IF |
Anti-Spike protein [SR4] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | Biolayer interferometry, FACS, NTRL, therapeutic, ELISA |
Anti-Spike protein [MR3] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | Biolayer interferometry, FACS, NTRL, therapeutic, ELISA |
Anti-Spike protein [Sb23] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | Biolayer interferometry, NTRL, ELISA |
Anti-Covid-19 & SARS-CoV Nucleocapsid [1C7C7] | Human IgG1, IgM, IgA1, IgG2 and IgG4-S228P; Mouse IgG1, IgG2a, IgM, Fab fragment and Fab2; Rabbit IgG; Ferret IgG1, IgM and IgA; Cat IgG1 and IgM | WB, ELISA, FC, IHC |
Anti-Spike protein [Ty1] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | Biolayer interferometry, inhibit, NTRL, ELISA, FC, IF |
Anti-Spike protein [MR17] | Human IgG1, IgM, IgG3, and IgA; Mouse IgG1; Rabbit IgG; VHH | Biolayer interferometry, FACS, NTRL, therapeutic, ELISA |
Absolute Antibody offers a range of recombinant antibodies against viral antigens. The antibodies were initially generated either through classic hybridoma technology, phage-display technology, or sequencing of (immortalized) B-cells from infected human patients. In particular we offer a range of antibodies generated by Humabs BioMed SA from real human patients using their Cellclone technology.
Our range of recombinant antibodies against epitope tags includes classic clones like 9E10 (anti c-myc) offered in multiple species and isotypes to suit your experiment.
Antibody Name [Clone] | Expected Species Reactivity | Applications |
Anti-Biotin [mAb2] | Species independent | ELISA |
Anti-Biotin [mAb7] | Species independent | ELISA |
Anti-Biotin [muM33] | Species independent | epitope tag, WB, ELISA |
Anti-c-myc epitope tag [9E10] | Human | IHC-F, IHC-P, IP, WB, IF |
Anti-CD56 [N901] | Human | IP, FC, IF |
Anti-DDDDK-tag [M2.1] | n/a | WB, ELISA, IF |
Anti-EE-tag [3D5/EE_48.K] | EE tag | WB, ELISA |
Anti-Flag tag [2H8] | Species independent | IP, FC, IF, IHC |
Anti-GCN4 [C11L34] | S. cerevisiae | IP, SPR, WB |
Anti-GSTP1 [SAIC-22D-22] | Human | immunoMRM |
Anti-HA Tag [16.43] | Virus (Influenza) | IP, WB, ELISA, FC, IF, IHC |
Anti-His tag (C-term) [3D5] | n/a | WB, ELISA |
Anti-IL-5 [JES1-39D10] | Human | immunocytochemistry, Block, ELISA, FC, IHC |
Anti-MBP [MBP-7128] | Escherichia coli | ELISA |
Anti-MBP [MCS2] | Escherichia coli | |
Anti-MBP [sAb-11M] | Escherichia coli | ELISA |
Anti-MBP [sAb-70] | Escherichia coli | ELISA |
Anti-MBP [sAb-P1] | Escherichia coli | ELISA |
Anti-Notch 1 [2E6] | Human | inhibit, Block |
Anti-Podoplanin (MAP tag) [PMab-1] | Mouse | epitope tag, WB, Block, ELISA, IHC |
Anti-Protein C [HPC-4] | Baboons, Human | Blocking, Purification, ELISA |
Anti-RAP tag [PMab-2] | Rat | epitope tag, WB, ELISA, FC, IHC |
Anti-Rhodopsin [Rho 1D4] | Cow, Human, Zebrafish, Amphibians, Rat, Mouse | IP, Radioimmune labeling, WB, ELISA, IF, IHC |
Anti-Rim ABC protein [Rim 3F4] | Cow, Xenopus laevis, Xenopus tropicalis, Human, Mouse | IP, WB, ELISA, IF, IHC |
Anti-Softag 1 [NT73] | E.coli | WB, ELISA |
Anti-Strep-Tag II [C23.21] | Streptomyces avidinii | WB, ELISA |
Anti-TK15 epitope tag [TK 15] | Xenopus laevis | IP, WB, IF |
Anti-V5 epitope tag [SV5-P-K] | Paramyxovirus Simian Virus 5 | IP, RIA, WB, ELISA, IF, IHC-Fr |
Bispecific antibodies are an exciting class of therapeutics permitting simultaneous engagement of two distinct targets with the same antibody. Knob-into-hole (KIH) bispecific antibodies are playing an important role in drug development, as this pioneering format enables heavy-chain heterodimerization and the creation of an IgG-like antibody with different targets on each arm. However, researchers have lacked syngeneic mouse models for evaluating KIH bispecific combinations, as the mutations applied to human IgG1 cannot be readily transferred to murine IgG subtypes.
To address this, Absolute Antibody has developed the first commercially available platform for the generation of fully murine KIH bispecific antibodies. Customers can purchase bispecific antibodies from our catalog off-the-shelf, or mix-and-match targets from the catalog to build their own custom reagent, to enable easier evaluations of potential bispecific combinations in mouse models.
Highlights of our murine KIH bispecific antibodies include:
For more information, download our research poster to learn about the generation of our KIH bispecific antibody platform and review functional characterization of our anti-mCD3ε:TRP-1 bispecific antibody, capable of selectively recruiting T-cells to TRP-1+ cancer cells for increased cytotoxic effector function. You can also read a customer case study about researchers at the Leiden University Medical Center who used two of our bispecific antibodies in a study that showed oncolytic viruses in combination with CD3ε-bispecific antibodies could improve the immunotherapy treatment of solid cancer tumors.
In addition to our KIH bispecific antibodies, further murine bispecific antibody constructs are available in an IgG-dAb format, enabling bivalent engagement of each target and representing further antibody engineering options available to our customers. To learn more about our suggested initial go-to formats for bispecific antibodies, as well as the utility of mouse bispecifics in basic research and drug discovery.
View our off-the-shelf bispecific antibodies below, and follow the links to place your order. Please contact us to discuss creating a custom bispecific reagent, using either clones from our catalog or your own antibodies. Starting with a hybridoma cell line, purified antibody or antibody sequence, we can deliver milligram-to-gram quantities of your custom bispecific, 100% royalty-free.
Targets | mCD3ε | hCD3ε | mPD-L1 | mCD47 | mOX40 | mCD28 |
mCD19 | mKIH | |||||
mCD20 | mKIH | |||||
mCTLA-4 | mKIH | mIgG-dAb | ||||
hEGFR | mKIH | |||||
hEGFRvIII | mKIH | |||||
herbB-2 (Her-2/neu) [Trastuzumab] | mKIH | mKIH | ||||
F4/80 | mKIH | |||||
Fluorescein | mKIH | mKIH | mKIH | |||
TRP-1 | mKIH | mKIH | mKIH | |||
mCD200 | mIgG-dAb | |||||
mPD-1 | mIgG-dAb | mIgG-dAb | ||||
mPDL1 | mKIH | mIgG-dAb | mIgG-dAb | mKIH | ||
mVISTA (PD-1H) | mIgG-dAb | |||||
mTIGIT | mIgG-dAb | |||||
mNKG2D | mKIH |
DNA and RNA are often thought of as mere information storages; however, the ability of nucleotide sequences to fold into defined structures has allowed nature to exploit these as catalytic and regulatory elements as well.
As our understanding of DNA- and RNA-biology continues to grow, new research tools are required to help us understand the impact on diverse branches of research such as cancer, immunology, aging and infectious disease. At Absolute Antibody, we offer a variety of recombinant engineered antibodies targeting nucleotide structures, in particular DNA and/or RNA primary, secondary and tertiary structures.
Our DNA/RNA research collection includes antibodies for classic structures, including single- or double-stranded DNA, dsRNA, hairpin DNA and Z-DNA, as well as antibodies for more recently discovered structures such as DNA/RNA hybrids, G-quadruplexes and i-Motif. Moreover, we are also featuring our collection of antibodies against naturally occurring or chemically induced modified nucleotide bases. All antibodies are recombinantly produced for ensured purity and batch-to-batch reproducibility.
Each antibody clone is available in a variety of species, isotypes and subtypes designed to increase experimental flexibility and antibody compatibility. For example, you can select a format to enable easier co-labelling studies or increase compatibility with a secondary reagent. You can also add a custom conjugation to allow for easier detection, or select a monomeric binder such as a Fab fragment or half-antibody to improve localization in super-resolution methods and maintain single-domain binding characteristics.
Antibody Name [Clone] | Expected Species Reactivity | Applications |
Anti-(6-4) DNA photoproducts [64M-2] | Species independent | ELISA, IF |
Anti-(6-4) DNA photoproducts [64M-5] | Species independent | ELISA, IF |
Anti-5-Hydroxymethylcytosine [AB3/63.3] | Species independent | Dot, IP, IF |
Anti-Cisplatin modified DNA [CP9/19] | Species independent | dotblot, IP, ELISA, IHC |
Anti-DNA-RNA hybrid [S9.6] | n/a | ABA, CHIP, ChIP-seq, DB, EMSA, FISH, ICC, IP, SPR, IF |
Anti-DNA/RNA G-quadruplex [BG4] | Human | EMSA, ELISA, IF |
Anti-Hairpin DNA [DNA-1] | WB, ELISA | |
Anti-i-motif DNA [iMab] | n/a | BLI, confocal microscopy, ELISA, IF |
Anti-N6-methyladenosine [17-3-4-1] | Saccharomyces cerevisiae, Human, Mouse | immunoblot, IP |
Anti-Quadruplex DNA [1H6] | Species independent | ELISA, IF, IHC |
Anti-Quadruplex DNA [4E11] | Species independent | ELISA, IHC |
Anti-Quadruplex DNA [5E11] | Species independent | ELISA, IHC |
Anti-Quadruplex DNA [8H2] | Species independent | ELISA, IHC |
Anti-single-stranded poly(rI) RNA [Jel 103] | Species independent | SPRIA, IF |
Anti-ss/dsDNA [A52] | Species independent | crystallize, RIA, ELISA |
Anti-ssDNA/dsDNA [m3D8] | Species independent | hydrolysis, SPR, ELISA |
Anti-Triplex DNA [Jel 466] | IF | |
Anti-Z-DNA [Z22] | Species independent | gel retardation assay, SPR, ELISA, IF |
Anti-F4/80 [Cl:A3-1] antibody is the most widely publicized and referenced mouse macrophage and microglia marker, making it a valuable tool for research.
At Absolute Antibody, we have sequenced the original hybridoma (rat anti-mouse F4/80 clone Cl:A3-1; Gordon and Austyn, 1981) and produced recombinant and chimeric anti-F4/80 clone Cl:A3-1 versions, allowing greater experimental flexibility and control for the end user (See Why Go Recombinant?).
F4/80 is a mature mouse cell surface glycoprotein and is a member of the epidermal growth factor (EGF)-transmembrane 7 (TM7) family. High level of expression is found on most tissue macrophages including the spleen, liver kupffer cells, microglia in the brain and skin Langerhans cells.
Absolute Antibody recombinant mouse anti-mouse and rat anti-mouse F4/80 Clone Cl:A3-1 are supplied in purified, azide-free, and low endotoxin versions to allow for in vivo applications.
If you cannot find F4/80 in the format you are looking for or would like to obtain a quote for bulk orders, please just get in touch.
Antibody Name [Clone] | Expected Species Reactivity | Applications |
Anti-F4/80 [Cl:A3-1 (recombinant version)] | Mouse | FC, IHC |
Negative controls are essential to conducting thorough and meaningful experiments. Antibodies can bind to other molecules, especially other proteins, in non-specific or undesired ways. To show that identification of a particular band on a Western Blot or staining for a cell-surface marker in flow cytometry using an antibody is specific, a negative control may be used which should not result in similar band patterns or staining.
Isotype controls are a particular type of negative control that feature the same Fc region as the antibody the actual experiment is being conducted with but a variable region that should not bind antigen in the experiment. The Fc region can interact specifically with Fc receptors or complement; hence, it is necessary to control for this “background” when staining for cell-surface markers. These interactions may even be across species; e.g., rat IgG with mouse Fc receptors. Therefore, a diverse panel of isotype controls was traditionally required when performing flow cytometry. See also our Fc Silent™ product range for practical solutions to this problem.
Antibody engineering makes possible the generation of a standardized panel of isotype controls with the same “specificity” (i.e., derived from the same original antibody) – this can reduce experimental complexity. The panels benefit from the superior reproducibility and purity we obtain using our recombinant production platform.
Absolute Antibody currently offers isotype-control panels derived from four different antibodies: anti-NP, anti-fluorescein, anti-beta galactosidase (from E. coli) and an antibody called MOPC-21 with unknown specificity. All are available in human, mouse, rat, rabbit and hamster isotypes.
Don’t see the format you need? Just contact us and we’ll be happy to help you.
Antibody Name [Clone] | Expected Species Reactivity | Applications |
Anti-Beta-galactosidase [13R4] | E. coli | negative control, WB, FC |
Anti-Beta-galactosidase [GL117] | E. coli | ELISA |
Anti-Fluorescein [4-4-20 (enhanced)] | n/a | negative control |
Anti-hapten 4-hydroxy-3-nitrophenyl acetyl (NP) [B1-8] | n/a | negative control |
Anti-Unknown Specificity (Isotype control) [MOPC-21] | n/a | negative control |
Tumor antigens serve as important tumor markers and can be used as targets in the detection and treatment of cancer. Antibodies targeting these tumor markers may have diagnostic applications in detection of the presence, type and stage of cancer. They also form an important class of therapeutic antibodies.
Absolute Antibody offers a large catalog of 75+ tumor marker antigens, including anti-TAA (tumor associated antigens) and anti-TSA (tumor specific antigens). We have used our recombinant antibody technology and antibody engineering to generate different engineered formats of these antibodies for all your experimental needs.
Highlights of our tumor marker antigens include:
View all of our off-the-shelf tumor marker antigens below and follow the links to place your order. If you would like to discuss creating a custom engineered antibody, please contact us. We are always happy to engineer our antibodies to fit your research needs. As we say – If you can describe it, we can make it.
Antibody Name [Clone] | Expected Species Reactivity | Applications |
Anti-A33 [huA33] | Human | deplete, ELISA, IF, IHC |
Anti-Alpha-fetoprotein (AFP) [AF5] | Human | WB, FC, IF |
Anti-Alpha-ketoglutarate-dependent dioxygenase alkB homolog 3 [32C8_71] | Human | DSF, SPR, ELISA |
Anti-Aspartate beta-hydroxylase [G3-F11] | Human | WB, ELISA, IHC |
Anti-BCL2 [bcl-2/100] | Human | IP, WB, IHC |
Anti-Beta-2 microglobulin [BBM.1] | Human | Depletion, WB, IF, IHC |
Anti-BLC2 [bcl-2/124] | Human | IP, WB, IHC |
Anti-Breast Epithelial Mucin [BrE-3] | Human | ELISA |
Anti-c-erbB-2 [FWP51] | Human | fusion, IP, FC, IF |
Anti-CA125 [196-14] | Human | ELISA, IHC |
Anti-CA125 [OC125-3.11] | Human | IP, WB, ELISA, FC, IF, IHC |
Anti-CA125 [VK-8-1.9] | Human | IP, WB, ELISA, FC, IF, IHC |
Anti-CA19-9 [4A6] | Human | ELISA |
Anti-CA19-9 [4G2] | Human | ELISA |
Anti-CA242 [C242] | Human | IHC |
Anti-CA242 [WT 1-31] | Human | ELISA |
Anti-CA50 [CA50Ab01] | Human | ELISA, IF |
Anti-Canine Lymphoma [Mab231] | Dog, Human | RIA, FC |
Anti-carcinoembryonic antigen (CEA) [Arcitumomab] | Human | IHC-P, FC, Imaging |
Anti-carcinoembryonic antigen [A5B7] | Human | radiolabelling, therapeutic, IHC |
Anti-CD155 [CD155.16 ] | Human | FC |
Anti-CD155 [scFv1] | Human | IP, FC |
Anti-CD155 [scFv3] | Human | functional assay |
Anti-CD155 [SKII.4] | Human | ICC, IP, ELISA, FC, IF, IHC |
Anti-CD19 [B4] | Human | FC, IF, IHC |
Anti-CEA [BW431/26] | Human | Immunoscintigraphy |
Anti-CEA [CH1A1A (2F1, CH1A1A-2F1)] | Human | ELISA, FC, IHC |
Anti-CEA [EB-011] | Human | ELISA |
Anti-CEA [EB-022] | Human | ELISA |
Anti-CEA [T84.66] | Human | Immunoscintigraphy, immunotherapy, RIA, ELISA, FC, IHC |
Anti-CIP2A [HL1925] | Human | IHC (P), WB |
Anti-CSAp [Mu-9] | Human | therapeutic, ELISA, IHC |
Anti-Ctip2 [25B6] | Guinea Pig, Rat, Zebrafish, Human, Cynomolgus Monkey, Mouse | CHIP, IHC-P, IP, WB, FC, IF, IHC-Fr |
Anti-Cytokeratin 7 [OV-TL 12/30] | Human | WB, FC, IF, IHC |
Anti-Cytokeratin 8 [TS1] | Human | IP, radioimmunotherapy, WB, ELISA, IHC |
Anti-deltaEGFR [DH8.3] | Human | IP, WB, ELISA, FC, IHC |
Anti-EGFR [2F8 (Zalutumumab; HuMax-EGFR)] | Human | WB, ELISA, FC |
Anti-EGFR [2224] | Human | FC |
Anti-EGFR [528] | Human | IHC-P, IP, NTRL, WB, FC, IF |
Anti-EGFR [C225 (Cetuximab)] | Human | Block, FC |
Anti-EGFR [cet.Hum (Cetuximab – humanized; hC225)] | Human | WB, Block, ELISA, FC |
Anti-EGFR [EGFR1] | Human | IP, WB, FC, IF, IHC |
Anti-EGFR [L2 1C] | Human | WB, ELISA, FC |
Anti-EGFR [L3 11D] | Human | SDS-PAGE, WB, ELISA, FC |
Anti-EGFR [Matuzumab] | Human | antagonist, WB, Block, ELISA, FC, IF |
Anti-EGFR [S3 12D] | Human | ICC, WB, ELISA, IF, IHC |
Anti-EGFR [S4 10H] | Human | WB, ELISA, FC |
Anti-EGFR domain III [h-R3 (Nimotuzumab)] | Human | Block, FC, IHC |
Anti-EGFRvIII [L8A4] | Human | Biacore, WB, ELISA, FC, IF, IHC |
Anti-Endosialin [scFv78] |
Human, Mouse
|
tumor imaging, ELISA, FC |
Anti-EPCAM [B38.1] | Human | RIA, ELISA |
Anti-erbB-2 (Her-2/neu) [4D5-8 (trastuzumab)] | Human | ELISA, FC, IHC |
Anti-ERBB2 [SAIC-02A-7] | Human | immunoMRM, WB, ELISA |
Anti-GA733-2 [FU-MK-1] |
n/a
|
IB, ICC, WB, ELISA, IHC |
Anti-GDF15 [Clone 29] | Human | functional assay, inhibit, WB, ELISA |
Anti-GDF15 [MBM-12] | Human | functional assay, inhibit, ELISA |
Anti-GDF15 [MBM-14] | Human | functional assay, inhibit, ELISA |
Anti-Glypican-1 [AbAb-GPC1] | Human | ELISA, FC |
Anti-Glypican-1 [AbAb2-GPC1] | Human | ELISA |
Anti-HER2 [4D5] | Human | crystallization, in vivo, inibition, IP, therapeutic, FC |
Anti-HER2 [C7b] | Human | cytometric bead array, WB, ELISA, FC, IHC |
Anti-HER2 [ML3-9 (C6ML3-9)] | Human | RIA, SPR, FC |
Anti-HER2/neu [SER4] | Human | ELISA |
Anti-HER3 [A5 ] | Human | SPR, FC |
Anti-HER4 [B6 (HER4.B6)] | Human | ELISA |
Anti-high MWT epithelial antigens [KC4G3] | Human | WB, IHC |
Anti-Human Ephrin Type A receptor 2 [1C1] | Human | agonist, internalizing, WB, ELISA, FC, IF |
Anti-JAM-A [6F4] | Human | WB, ELISA, FC, IF, IHC |
Anti-KRAS G12C mutant [AbAbKRAS01] | Human | WB, ELISA |
Anti-KRAS G12D mutant [D113] | Human | ELISA |
Anti-Lewis Y [3S193] | Human | humanisation, ELISA, IHC |
Anti-LeY [BR96] | Human | ELISA, IHC |
Anti-LeY [H18A] | Human | ELISA, IHC |
Anti-LMP1 [H3] |
Epstein-Barr virus (EBV)
|
inhibit, IP, ELISA, IF |
Anti-m5C [FMC-9] |
Species independent
|
ICC, IPP, WB, ELISA, IHC |
Anti-MAGEA3 [21B4] | Human | IP, WB, ELISA, FC, IHC |
Anti-Mesothelin [11-25] | Human | IP, ELISA, FC |
Anti-Mesothelin [C10] | Human | SPR, ELISA, IHC |
Anti-Mesothelin [IC14-30] | Human | ELISA |
Anti-Mesothelin [K1] |
Cynomologous monkey, Human
|
RIA, SPR, WB, ELISA, IF, IHC |
Anti-MPF [20-10] | Human | IP, WB, ELISA |
Anti-MPF [41-28] | Human | IP, WB, ELISA |
Anti-MUC1 [E29] | Human | WB, IHC |
Anti-MUC1 [HMFG1 (1.10.F3)] | Human | ICC, IP, ELISA, FC, IF, IHC |
Anti-MUC1 [HMFG2] | Human | ELISA, IHC, Imaging |
Anti-MUC1 [Mc5] | Human | IP, IRA, WB, ELISA, IHC |
Anti-MUC1 [PAM4] | Human | therapeutic, WB, ELISA, FC, IHC |
Anti-MUC1 [SM3] | Human | ELISA; IHC-P, FC, IHC-Fr |
Anti-NSE [E1-7E2] | Human | WB, ELISA |
Anti-NSE [E2-4F6] | Human | WB, ELISA |
Human | deplete, ELISA, IF, IHC | |
Dog, Human | WB, FC, IF | |
Dog, Human | DSF, SPR, ELISA | |
Human, Mouse | WB, ELISA, IHC | |
Human | IP, WB, IHC | |
Human | Depletion, WB, IF, IHC | |
Monkey, Rabbit, Rat, Human, Mouse | IP, WB, IHC | |
Human | ELISA | |
Human | fusion, IP, FC, IF | |
Human | ELISA, IHC | |
Human | IP, WB, ELISA, FC, IF, IHC | |
Human | IP, WB, ELISA, FC, IF, IHC | |
Anti-CA19-9 [4A6]
|
Human | ELISA |
Anti-CA19-9 [4G2]
|
Human | ELISA |
Anti-CA242 [C242]
|
Human | IHC |
Anti-CA242 [WT 1-31]
|
Human | ELISA |
Anti-CA50 [CA50Ab01]
|
Human | ELISA, IF |
Dog, Human
|
RIA, FC | |
Human | IHC-P, FC, Imaging | |
Human | radiolabelling, therapeutic, IHC | |
Anti-CD155 [CD155.16 ]
|
Human | FC |
Anti-CD155 [scFv1]
|
Human | IP, FC |
Anti-CD155 [scFv3]
|
Human | functional assay |
Anti-CD155 [SKII.4]
|
Human | ICC, IP, ELISA, FC, IF, IHC |
Human | FC, IF, IHC | |
Human | Immunoscintigraphy | |
Human | ELISA, FC, IHC | |
Human | ELISA | |
Human | ELISA | |
Human | Immunoscintigraphy, immunotherapy, RIA, ELISA, FC, IHC | |
Anti-OA3 [OV-TL3] | Human | IB, WB, Block, ELISA, IF, IHC |
Anti-osteosarcoma-associated cell membrane antigen [TP-1] |
Dog, Human
|
radioimmunodetection, IF, IHC |
Anti-osteosarcoma-associated cell membrane antigen [TP-3] |
Dog, Human
|
radioimmunodetection, IF, IHC |
Anti-p21 [Y13-238] |
Human, Mouse
|
IP; |
Anti-p21Ras [DWP] | Human | WB, ELISA, IHC |
Anti-p21Ras [KGH-R1] | Human | ICC, IHC-FFPE, WB, ELISA, IF |
Anti-p53 [PAb421] |
Monkey, Rabbit, Rat, Human, Mouse
|
IHC -P, in vivo, IP, WB, ELISA, IF, IHC-Fr |
Anti-polymorphic epithelial mucin [CTM01] | Human | IP, therapeutic, IHC |
Anti-PSA [8G8F5] | Human | ELISA |
Anti-PSA [scFv B8] | Human | SPR, WB |
Anti-PSMA [11d1e5E10] | Human | ELISA, IHC |
Anti-PSMA [J591] | Human | IP, therapeutic, WB, ELISA, FC, IF, IHC |
Anti-S100 [S1-61] | Human | WB, IHC |
Anti-S100B [1C8] | Human | therapeutic, ELISA |
Anti-Synaptophysin [SP15] |
Cat, Hamster, Pig, Rat, Human
|
WB, ELISA, IHC |
Anti-TAG-72 [Minretumomab (CC49 )] | Human | RIA, therapeutic, WB, FC, IHC |
Anti-Tenascin [I-81C6 (Neuradiab)] | Human | cross-competition assay, immunoreactivity, radioiodination, ELISA |
Anti-Tn Antigen [237mAb] |
Human, Mouse
|
WB, ELISA |
Anti-trastuzumab (anti-idiotype) [scFv40] | Human | immunogen, Block |
Anti-trastuzumab (anti-idiotype) [scFv69] | Human | immunogen, Block |
Anti-TRP-1, gp75 [TA99] | Human | IP, WB, ELISA, FC, IF, IHC-Fr |
Anti-Tumor associated glycoprotein (TAG) 72 [B72.3 (Satumomab)] | Human | FC, IHC, Imaging |
Anti-VAP-1 [2D10] | Human | IP, WB, ELISA, FC, IHC |
Anti-VAP-1 [3F10] | Human | ELISA, IHC |
Anti-VAP-1 [3G6] | Human | ELISA, IHC |
Anti-VAP-1 [TK8-14] | Human | IP, WB, ELISA, FC, IHC |
Tumor suppressor proteins are crucial for maintaining cell balance and curbing uncontrolled growth and studying them and their possible loss-of-function is key in advancing cancer research. When tumor suppressors are inactive, cancer can proliferate. Antibodies serve as vital tools in understanding tumor suppressor proteins, allowing precise detection and localization in experiments. Absolute Antibody is committed to supporting scientific progress by offering antibodies tailored for tumor suppressor research. By leveraging these antibodies, researchers gain a refined toolkit to explore and manipulate tumor suppressor functions, paving the way for innovative cancer therapies and contributing to the broader landscape of oncological research.
The p53 tumor suppressor protein regulates cell growth and prevents the formation of tumors. It acts as a “guardian of the genome” (Park et al., 2016), overseeing DNA repair and, when necessary, triggering apoptosis to eliminate damaged cells. P53 antibody studies are vital because they allow researchers to investigate the protein’s levels, activity, and interactions with precision. Understanding p53’s role and dysregulation in cancer is essential for developing targeted therapies and improving overall strategies for cancer treatment.
Immunofluorescence staining of fixed A431 with anti-p53 antibody PAb421 (Ab00142). Published applications of this clone are IHC-P, in vivo, IP, WB, ELISA, IF, and IHC-Fr.
Immunofluorescence staining of A431 cells with anti-p53 (a.a. 16-25) (Ab02776) X77. Published applications of this clone are IP, WB, ELISA, and IF.
Immunofluorescence staining of A431 cells with anti-p63 (Ab00871) BU5. Published applications of this clone are FC and IF.
TP63, a member of the p53 tumor suppressor gene family, encodes for the p63 protein, which regulates epithelial development and maintains genomic stability (Melino, 2011). Unlike p53, TP63 is not commonly associated with direct tumor suppression but is pivotal for controlling cellular differentiation and maintaining epithelial integrity. Multiple promoters and splice variants give rise to various isoforms of this protein. Studying TP63 in cancer research using antibodies is important for understanding its expression patterns, isoform-specific functions, and potential involvement in various cancers. TP63 antibody assays give researchers insight into the roles of TP63 in normal and aberrant cellular processes and thus its potential implications in cancer development and progression. TP63’s distinct functions in epithelial biology differentiate it from traditional tumor suppressors, making it a subject of interest for researchers investigating its nuanced contributions to cancer biology.
The p16 tumor suppressor protein, encoded by the cyclin-dependent kinase inhibitor 2A (CDKN2A) gene, regulates the cell cycle by inhibiting the activity of cyclin-dependent kinases, specifically CDK4 and CDK6, which are involved in promoting cell cycle progression. In inhibiting these kinases, p16 helps prevent uncontrolled cell division and suppresses tumor formation (Li et al., 2012). Unlike p53, which is involved in a broader range of cellular responses, p16 is more specifically focused on cell cycle regulation. Its importance in cancer research is underscored by its frequent inactivation or loss in various cancers, leading to unrestrained cell proliferation. A highly defined P16 antibody is an essential tool in studying p16 as it enables researchers to assess expression levels, localization, and interactions, providing crucial insights into p16’s role in maintaining cell cycle control and its implications for cancer development and treatment. Our recombinant anti-p16 antibody is based on the clone 30859-S17 which has been cited for use in western blot, ELISA, and IHC applications. Additionally, we have engineered this clone from its original mouse IgG1 version into rabbit IgG to decrease cross-reactivity and background signal in human tissues.
KRAS mutations, specifically G12V, G12C, and G12D, are biomarkers associated with various cancers, particularly colorectal cancer and non-small cell lung cancer (Gao & Shen, 2022). These mutations result in the constitutive activation of the KRAS protein, leading to uncontrolled cell growth and tumor progression. Studying KRAS G12V, G12C, and G12D in cancer research using antibodies is crucial for understanding their expression patterns, localization, and activity levels. Like inactivated tumor suppressors, KRAS mutations represent an oncogenic driver, promoting tumorigenesis, and KRAS protein antibodies play a pivotal role in dissecting the aberrant signaling pathways associated with KRAS mutations, providing essential information for the development of targeted therapies. One such KRAS antibody is the anti-p21Ras clone DWP which has been cited for use in western blot, ELISA, and IHC and recognizes the KRAS mutant peptides G12V and G12C. Our recombinant version has been engineered from the original mouse IgG2b to such formats as mouse IgG2b Fc Silent™ with abrogated Fc binding for reduced non-specific staining. Other formats include human IgG1 with and without Fc binding functionality, and rabbit IgG.
Transforming Growth Factor-beta (TGF-β) is a multifunctional cytokine that plays a dual role in cancer, acting as both a tumor suppressor and a promoter, depending on the context (Seoane & Gomis, 2017). In its role as a tumor suppressor, TGF-β helps regulate cell growth, inhibit cell proliferation, and promote apoptosis. However, during later stages of cancer progression, TGF-β can paradoxically stimulate tumor growth and metastasis. Studying TGF-β in cancer research using antibodies is essential for elucidating its complex role in tumorigenesis. Antibodies enable researchers to investigate the levels, activity, and interactions of TGF-β, providing critical insights into its dynamic functions and potential as a therapeutic target in cancer treatment.
Cadherin-1: Cadherins, particularly cadherin-1 (or E-cadherin) act as tumor suppressors by preserving cellular adhesion. Anti-cadherin antibodies are instrumental in researching tumor suppressors, allowing specific detection and quantification of cadherin levels, uncovering insights into mechanisms driving tumor progression.
Retinoblastoma protein: Retinoblastoma protein (Rb) is coded for by the RB1 gene, the first described human tumor suppressor gene (Berry et al., 2019), making Rb a pioneer protein for the study of tumor suppressors. Its importance in research has not dwindled, as Rb is central to cell cycle regulation and its downregulation and inactivation can lead to uncontrolled cell growth. We offer the recombinant engineered version of the anti-RBBP5 clone RAB-C379, cited for use in immunoprecipitation mass spectrometry and immunofluorescence assays.
SMARCA4: SMARCA4, also known as BRG1, is a tumor suppressor involved in chromatin remodeling. Mutations or loss of SMARCA4 function are observed in various cancers, notably small cell carcinoma of the ovary. Anti-SMARCA4 antibodies play a crucial role in studying this tumor suppressor, enabling specific detection and quantification, and providing insights into its contribution to cancer development. The anti-Brg1 clone 4E5 has published applications in immunoprecipitation, western blot, immunofluorescence, and immunohistochemistry. We recombinantly engineered anti-Brg1 [4E5] for more experimental options into various human, mouse, and rat IgG isotypes, including Fc Silent™ options on some formats for tailed effector function.
Catenin beta-1: Catenin beta-1 (encoded by CTNNB1), also known as β-catenin, is a key player in the Wnt signaling pathway and is integral to cell adhesion. Unique in the study of tumor suppressors, β-catenin functions both as a structural component in cell adhesion complexes and as a transcriptional co-activator in the nucleus. Dysregulation of β-catenin is often associated with various cancers, making anti-catenin beta-1 antibodies essential tools for specific detection and quantification. These antibodies contribute significantly to understanding the dual role of β-catenin and its involvement in cancer initiation and progression.
Absolute Antibody’s recombinant engineered antibodies, available in diverse formats and species, are essential tools for studying tumor suppressors. They enable specific detection and quantification of protein expression, including isoform-specific analysis. These antibodies facilitate functional studies, allowing manipulation of tumor suppressor activity, and can be utilized in high-throughput screening for drug discovery. Their species compatibility supports research across various organisms, contributing to the understanding of tumor suppressor biology.
Additionally, the recombinant antibodies we offer are 100% biologically defined, opening further opportunities for our antibody engineers to customize these tools to your exact experimental needs. For more information on our custom services, we have resources available on formats we have made (including bi-, tri-, and multispecific formats), our recombinant production platform, and more. If your questions still aren’t answered, reach out! Our team is happy to help with any product questions or orders.
As an Absolute Biotech brand, Absolute Antibody is proud to partner with our sister companies to provide an even more comprehensive menu of antibody-based research tools. Other reagents include:
Catalog ID | Target | Antibody Clone | Formats Available |
Ab00142 | p53 | PAb421 | Mouse IgG2a Rabbit IgG |
Ab03148 | p53 | 70237-85 | Rabbit IgG Mouse IgG2a |
Ab02776 | p53 | a.a. 16-25 | Mouse IgG1 Human IgG1 Human IgG1 Fc Silent Rabbit IgG |
Ab03149 | p16 | 30859-S17 | Human IgG1 Rabbit IgG Mouse IgG1 Human Fab fragment Mouse Fab fragment |
Ab03149 | p16 | 30859-S17 | Mouse IgG2a Rabbit IgG |
Ab04234 | KRAS G12V | G12V-34 | Mouse IgG1 Rabbit IgG scFv fragment (His) |
Ab03878 | KRAS G12C mutant | AbAbKRAS01 | Human IgG1 Human IgG1 Fc Silent Mouse IgG1 Rabbit IgG |
Ab03877 | KRAS G12D mutant | D113 | Rabbit IgG Mouse IgG1 Human IgG1 Human IgG1 Fc Silent |
Ab03876 | p21Ras | DWP | Mouse IgG2b Fc Silent Human IgG1 Human IgG1 Fc Silent Mouse IgG2b Rabbit IgG |
Ab03875 | p21Ras | KGH-R1 | Rabbit IgG Mouse IgG2b Human IgG1 Fc Silent Human IgG1 Mouse IgG2b Fc Silent |
Ab02466 | TGF-beta1 | 2H4 | Rabbit IgG Human IgG1 Human IgG1 Fc Silent Mouse IgG1 |
Ab03786 | TGF beta1 | SL15S | Human IgG1 scFv fragment (His) |
Ab03951 | TGF beta | 1D11.16.8 | Rabbit IgG Human IgG1 Human IgG1 Fc Silent Mouse IgG1 |
Ab02465 | Latent TGF-beta1 | 2F10 | Rabbit IgG Human IgG1 Human IgG1 Fc Silent Mouse IgG1 |
Ab03702 | GDF15 | MBM-14 | Rabbit IgG Mouse IgG2b Fc Silent Mouse IgG2b Human IgG1 Human IgG1 Fc Silent scFv fragment (His) |
Ab03701 | GDF15 | MBM-12 | Rabbit IgG Mouse IgG2b Fc Silent Mouse IgG2b Human IgG1 Human IgG1 Fc Silent scFv fragment (His) |
Ab03700 | GDF15 | Clone 29 | Rabbit IgG Mouse IgG2b Fc Silent Mouse IgG2b Human IgG1 Human IgG1 Fc Silent |
Ab01853 | RBBP5 | RAB-C379 | Human IgG1 Rabbit IgG Mouse IgG1 Human Fab fragment Mouse Fab fragment |
Ab00871 | p63 | BU5 | Mouse IgG2b Fc Silent Rabbit IgG Human IgG1 Mouse IgG2b |
Ab03151 | p40 | 14D5E8F12 | Rabbit IgG Mouse IgG1 |
Ab03150 | p63 | 60738-10D8 | Rabbit IgG Mouse IgG1 |
Ab00923 | p21 | Y13-238 | Rat IgG2a Rabbit IgG Mouse IgG1 Mouse IgG2a Mouse IgG2a Fc Silent Human IgG1 Human IgG1 Fc Silent Human IgG4-S228P |
Ab03219 | p21 | Y13-259 | Rabbit IgG Rat IgG1 Human IgG1 Human IgG1 Fc Silent |
Ab02737 | Gelsolin | GsnVHH 13 | Human IgA-Fc fusion Mouse IgG1-Fc fusion Rabbit IgG-Fc fusion |
Ab02738 | Gelsolin | GsnVHH 11 (Nb11) | Human IgA-Fc fusion Mouse IgG1-Fc fusion Rabbit IgG-Fc fusion |
Ab01654 | alpha catenin | 1G5 | Mouse IgG1 Rabbit IgG Human IgG1 Human IgG1 Fc Silent Human IgG4-S228P |
Ab02695 | p120/catenin | 2B12 | Mouse IgG1 Human IgG1 Human IgG1 Fc Silent Rabbit IgG |
Ab01655 | beta catenin | 15B8 | Mouse IgG1 Rabbit IgG Human IgG1 Human IgG1 Fc Silent Human IgG4-S228P |
Ab03193 | B-catenin | 3B1D11A8 | Rabbit IgG Mouse IgG1 Human IgG1 |
Human antibodies from patients are being sequenced at an increasing rate – see Quake et al. for an up-to-date review of high-throughput sequencing of antibodies. Amongst others, we are excited to offer you a range of human-derived antibodies specific to viral pathogens or self-antigen (many in collaboration with Humabs BioMed SA, Bellinzona, Switzerland). Our proprietary cloning platform allows us to produce high-quality recombinant versions of these antibodies – we think some will be valuable reagents for research and diagnostics. We offer the original human IgG version as well as reformatted mouse and rabbit versions to suit your experimental requirements- contact us for bulk custom orders.
Adjacent figure shows: Indirect immunofluorescence (IF) staining of live keratinocyte monolayers with pemphigus vulgaris (PV) auto-antibodies
(A) Cryosections of human skin stained with biotinylated DSG3-specific monoclonal antibodies (Ab00153, Ab00155, Ab00158 and Ab00156).
(B) Binding of a panel of pemphigus auto-antibodies to DSG3-coated ELISA plates in the presence or absence of EDTA. Antibodies described in (external links): Corti D et al. 2010 as well as Di Zenzo G et al. 2012.
(C) Staining of human epidermis with biotinylated PVB28 (Ab00158) in the presence (with) or absence (w/o) of Ca2+
Antibodies against proteins involved in co-stimulation and other aspects of immune cell regulation are of particular interest to therapeutics developers. Some have already entered the clinic, with more in the development pipeline. However, many aspects of immune cell signaling are still unknown, and researchers require ever more advanced tools to tap into this potential. Absolute Antibody has developed a collection of recombinant engineered antibodies against clinically relevant proteins, including mouse homologues of current therapeutic targets.
Contact us if you have any questions or would like a quote.
See also: Our Fc fusion proteins are matched to our collection of immunotherapy antibodies, with all products available in a range of species-specific and engineered Fc domains.
Catalog ID | Mouse Target | Antibody Clone | Original Antibody Format |
Ab01052 | 4-1BB (CD137) | LOB12.3 | Rat IgG1 |
Ab01054 | 4-1BBL (CD137L) | AT113-2 | Rat IgG1 |
Ab00881 | 4-1BBL (CD137L) | TKS-1 | Rat IgG2a |
Ab01027 | BTLA | HMBT-6B2 | Hamster IgG |
Ab00670 | CD27 | LG.3A10 | Hamster IgG |
Ab00895 | CD27 | RM27-3E5 | Rat IgG2a |
Ab00286 | CD28 | E18 | Mouse IgG2b |
Ab00285 | CD28 | D665 | Mouse IgG1 |
Ab01109 | CD40 | 3/23 | Rat IgG2a |
Ab01087 | CD40L (CD154) | MR1 | Hamster IgG |
Ab00816 | CD70 | TAN 1-7 | Rat IgG2a |
Ab01056 | CD70 | TAN1-6 | Rat IgG2a |
Ab01028 | CD80 (B7-1) | RM80 | Rat IgG2a |
Ab01029 | CD86 (B7-2) | PO.3 | Rat IgG2b |
Ab01089 | CD153 | RM153 | Rat IgG2b |
Ab01297 | CD96 | 6A6 | Rat IgG2a |
Ab00894 | CTLA-4 | 9H10 | Hamster IgG2 |
Ab01018 | CTLA-4 | 9D9 | Mouse IgG2b |
Ab01088 | GAL-9 | RG9-35 | Rat IgG2a |
Ab01060 | GITR | DTA-1 | Rat IgG2a |
Ab00374 | GITR | YGITR 860.103.5 | Rat IgG2b |
Ab00631 | GITR | YGITR765 | Rat IgG2b |
Ab00630 | GITRL | YGL386 | Rat IgG1 |
Ab01026 | HVEM | HMHV-1B18 | Hamster IgG |
Ab00814 | ICOS | 7E.17G9 | Rat IgG2b |
Ab00882 | ICOSL | HK5.3 | Rat IgG2a |
Ab01295 | LAG3 | C9B7W | Rat IgG1 |
Ab01295 | LAG3 | C9B7W | Rat IgG1 |
Ab00110 | OX40 (CD134) | OX86 | Rat IgG1 |
Ab00564 | OX40L | OX-89 | Rat IgG1 |
Ab00813 | PD-1 | RMP1-14 | Rat IgG2a |
Ab01017 | PD-1H (VISTA) | mam82 | Mouse IgG1 |
Ab01016 | PD-1H (VISTA) | MH5A | Hamster IgG |
Ab00373 | PD-L1 | YDC 127.1.1 | Rat IgG2a |
Ab00883 | PD-L2 | TY25 | Rat IgG2a |
Ab00875 | PDPN (MAP-Tag) | PMab-1 | Rat IgG2a |
Ab00973 | TIGIT | 4D4 | Hamster IgG |
Ab01258 | TIGIT | 1B4 | Mouse IgG1 |
Ab01032 | TIM-1 | 3B3 | Rat IgG2a |
Ab01110 | TIM-2 | RMT2-14 | Rat IgG2a |
Ab01057 | TIM-3 | 2C12 | Rat IgG1 |
Ab01058 | TIM-4 | 5G3 | Rat IgG1 |
Ab01059 | TIM-4 | 3A1 | Rat IgG1 |
Our research-grade biosimilars are research tools for the study and evaluation of biological processes without the need to source and purchase costly therapeutic-grade biologics. Free of excipients and/or additives found in the therapeutic formulations, our biosimilars require fewer extra controls in an experimental setting. In addition to the original human format, our biosimilars are available with mouse, rabbit, rhesus monkey and cynomolgus monkey constant domains.
Absolute Antibody research-grade biosimilars can be used as controls:
The growing range of research-grade biosimilars available from Absolute Antibody includes Trastuzumab, Muromonab, Campath-1H, Rituximab, Infliximab, Daclizumab, Basiliximab, Cetuximab, Satumomab, Acritumomab, Abaciximab, Eculizumab, Efalizumab, Clenoliximab, Ruplizumab, Matuzumab, Humicade, Volociximab and our most recent addition Oxelumab.
Can’t see what you were looking for? We can custom make any biosimilar of your choice – just send us the sequence. Contact us here.
For further information, to request any antibody in a different format, or for bulk orders please contact us and we’ll be happy to help you.
VivopureX™ antibodies are recombinant mouse antibodies ideal for in vivo research in mouse models. The collection consists of popular antibody clones, many originally obtained from rats or hamsters, which Absolute Antibody has engineered into mouse-anti-mouse recombinant versions to improve research results. These species-matched chimeric antibodies consist of a clone’s original antigen-binding variable domain with a mouse constant domain.
Our VivopureX™ recombinant mouse antibodies offer many advantages compared to the original antibody format, including:
Mean tumor sizes in animals treated with PD-1 mouse IgG2a Fc Silent™ antibody based on clone RMP1-14 (Ab00813-2.3) are significantly smaller than in animals treated with the traditional rat IgG2a antibody (Ab00813-7.1)
Our data illustrate how VivopureX™ mouse antibodies provide increased long-term efficacy, potency and consistency compared to the original rat antibodies. In the figure to the left, our recombinant mouse PD-1 antibody based on the widely used clone RMP1-14 reduced tumor size in a mouse model more effectively than the original rat version.
Looking for another example? One of our customers used a species-matched mouse-anti-mouse antibody to deplete CD8+ T-cells in mice more completely and for longer than the original rat antibody.
The VivopureX™ antibody collection includes a selection of our most exciting mouse-anti-mouse antibodies, now available at competitively priced bulk prices. All are available in discounted bulk sizes ranging from 1 mg to 100 mg, as well as our standard 200 µg size. In addition, we offer our recombinant isotype controls at up to 50% discount if purchased together with a linked VivopureX™ antibody. Contact us to receive a quote.
We’ll continue to add new antibodies to the list below, so check back for updates! Contact us with questions, to receive a quote, or to ask if another antibody could be made available in a mouse-anti-mouse format in bulk for in vivo research.
Antibody Name [Clone] | Engineered Format | Top Application | Available Bulk Sizes |
Anti-OX40/CD134 [OX86] | Mouse IgG1 | Agonism | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-OX40/CD134 [OX86] | Mouse IgG2a | Agonism | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-PD-1 [RMP1-14] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CTLA-4 [9D9] | Mouse IgG2a | Blocking, Treg depletion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CTLA-4 [9D9] | Mouse IgG2a Fc Silent™ | Blocking, peripheral Treg expansion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-GITR [DTA-1] | Mouse IgG2a | Agonism | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD25 [PC-61.5.3] | Mouse IgG2a | Depletion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-TIGIT [1B4] | Mouse IgG1 | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-TIGIT [1B4] | Mouse IgG2a | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-Lag3 [C9B7W] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD96 [6A6] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-IL-10R [1B1.3a] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-BTLA [HMBT-6B2] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-Tim-4 [3A1] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-Tim-4 [5G3] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-TIM-2 [RMT2-14] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-Tim-1 [3B3] | Mouse IgG1 | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-Tim-3 [2C12] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD115/M-CSFR [AFS98] | Mouse IgG2a | Depletion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-PD-L1 [10F.9G2] | Mouse IgG2b | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-PD-L1 [10F.9G2] | Mouse IgG2b Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-IFN-gamma receptor 1 [GR20] | Mouse IgG2b Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD20 [18B12] | Mouse IgG2a | Depletion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD4 epitope A [YTS 177.9] | Mouse IgG2a | Depletion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD4 epitope A [YTS 191.1] | Mouse IgG2a | Depletion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD8 alpha/Lyt-2 [YTS 169.4] | Mouse IgG2a | Depletion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-Ly6G [1A8] | Mouse IgG2a | Depletion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD200R [OX131] | Mouse IgG1 Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-PD-L2 [TY25] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-Ly6G/Ly6C [RB6-8C5] | Mouse IgG2a | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-Galectin 9 [RG9-35] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD153 [RM153] | Mouse IgG2a | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD153 [RM153] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD155 [3F1] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD226 [10E5] | Mouse IgG2a Fc Silent™ | Depletion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD45R [RA3-6B2] | Mouse IgG2a | Depletion | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD19 [6D5] | Mouse IgG2a | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-HVEM [HMHV-1B18] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD27 [RM27-3E5] | Mouse IgG1 | Agonism | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD22 [OX-97] | Mouse IgG2a Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD47 [mIAP301] | Mouse IgG2b Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Anti-CD80 [RM80] | Mouse IgG2b Fc Silent™ | Blocking | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
Engineered recombinant antibodies for a variety of research areas and applications.
Anti-immunoglobulin antibodies are important reagents used in the detection of antibodies. This may be in the form of a secondary antibody used to detect a primary antibody in methods such as western blot, immunohistochemistry, and immunofluorescence staining for microscopy or flow cytometry. Moreover, anti-immunoglobulin antibodies are important components of diagnostic tests. For example, they may be used in the characterization of immune responses or as control capture lines on lateral flow immunoassays.
Recombinant antibody technology allows you to obtain highly reliable anti-immunoglobulin antibodies tailored to your specific assay. Recombinant production provides the highest possible batch-to-batch reproducibility, while antibody engineering can be used to increase antibody compatibility with other assay components and extend antibody utility beyond the original format. Moreover, all our antibodies are manufactured in a completely animal- and animal-component free production platform.
We are pleased to announce our panel of recombinant anti-human immunoglobulin antibodies. The panel includes antibodies for human IgG, IgM, IgE and IgD, as well as anti-human kappa and lambda light chain antibodies for detection of all human antibodies. Available formats include human, mouse, rabbit and goat backbones, as well as antibody fragments, with other formats available upon request.
The panel is already proving popular among researchers fighting the current coronavirus pandemic, in light of the need for improved serological testing. These antibodies can be used to test for anti-SARS-CoV-2 antibodies in COVID-19 diagnostic tests
View our collection below, and contact us with any questions, to obtain an order quote, or to request pricing for bulk amounts.
Antibody Name [Clone] | Species Reactivity | Catalog Number |
Anti-IgG [17F12] | Human | Ab01176 |
Anti-IgG [8E11] | Human, chimpanzee, mangabey, vervet | Ab01270 |
Anti-IgG [8F1] | Human, non-human primates | Ab01271 |
Anti-IgG [NH3/130.5.2] | Human | Ab00854 |
Anti-IgG3 [NH3/15.8] | Human | Ab00856 |
Anti-IgM [M15/8] | Human | Ab00292 |
Anti-IgE [huMaE11 (Omalizumab)] | Human | Ab00717 |
Anti-IgE [TES-C21] | Human | Ab00497 |
Anti-IgD [IgD26] | Human | Ab01328 |
Anti-Lambda light chain [N10/2] | Human | Ab01326 |
Anti-Kappa light chain [NH3/41.34] | Human | Ab00855 |
Anti-IgA [H15A43] | Human | Ab02044 |
Anti-IgM [B481] | Human | Ab02047 |
Anti-human immunoglobulin [X1237M] | Human | Ab02048 |
Non-human-primate (NHP) models are important in preclinical research and are used as proxies for human immune responses. To help researchers investigate these, we offer a panel of recombinant anti-NHP immunoglobulin antibodies. This panel includes antibodies against key antibody isotypes and subtypes in widely used NHP models, such as rhesus macaque, cynomolgus monkey and baboon.
Anti-immunoglobulin antibodies are important reagents used in the detection of antibodies. Our NHP immunoglobulin antibodies can be used as secondary antibodies to detect primary antibodies in methods such as western blot, immunohistochemistry, and immunofluorescence staining for microscopy or flow cytometry. In addition, anti-immunoglobulin antibodies are important components of assays evaluating immune responses during cancer and autoimmunity drug development, infectious disease studies, and vaccine trials. Most recently, anti-immunoglobulin antibodies are finding extensive application in the study of COVID-19, as well as development of vaccines against SARS-CoV-2.
Recombinant antibody technology allows you to obtain highly reliable anti-immunoglobulin antibodies tailored to your specific assay. Recombinant production provides the highest possible batch-to-batch reproducibility, while antibody engineering can be used to increase antibody compatibility with other assay components and extend antibody utility beyond the original format. Moreover, all our antibodies are manufactured in a completely animal- and animal-component free production platform.
Our recombinant NHP immunoglobulin antibodies are available in formats such as human, mouse, and rabbit backbones, as well as antibody fragments. Other formats are available upon request and further targets will be added regularly – if there is anything specific you’re looking for and can’t find yet, please contact us.
View our NHP immunoglobulin antibodies below. If you are looking for secondary antibodies to human antibodies see here; for any other species, check out our page here. Finally, if you need primary antibodies with a non-human primate backbone, get in touch. Our entire recombinant antibody catalog is available in rhesus macaque and cynomolgus monkey IgG1 and IgG4 isotypes. If there is a particular antibody you cannot find in these formats, please contact us.
Antibody Name [Clone] | Species Reactivity | Catalog Number |
Anti-Macaque pan-species IgG [1B3] | Rhesus macaque; cynomolgus monkey; pigtailed macaque; baboon | Ab01269 |
Anti-Pan-primate IgG [8F1] | Human; non-human primates | Ab01271 |
Anti-Rhesus IgA alpha chain [10F12] | Rhesus macaque | Ab01272 |
Anti-Marmoset IgG [4H12] | Common marmoset; squirrel monkey | Ab01273 |
Anti-Baboon IgG1 [7H4.G8.G10] | Baboon | Ab01619 |
Anti-Baboon IgG2 [1E11.1] | Baboon | Ab01620 |
Anti-Baboon IgG3 [4A6.1] | Baboon | Ab01621 |
Anti-Baboon IgG4 [5F3.E11.G4] | Baboon | Ab01622 |
Anti-Rhesus IgG1 [3C10.3] | Rhesus | Ab01623 |
Anti-Rhesus IgG4 [2C6] | Rhesus | Ab01624 |
Anti-Rhesus IgG4 [7A8] | Rhesus | Ab01625 |
The majority of secondary antibodies against antibodies from common research models such as mouse or rat are polyclonal antibodies made in goats or rabbits. These not only suffer from reproducibility issues, but also come with a considerable impact on animal welfare. At Absolute Antibody, all our antibodies, including our secondary antibodies, are manufactured in a recombinant, completely animal- and animal-component free production platform. We are able to offer recombinant anti-immunoglobulin antibodies against mouse or rat antibodies, as well as antibodies that bind rabbit, goat, dog, and elasmobranch (e.g. sharks, rays, skates) antibodies.
Anti-immunoglobulin antibodies are used as secondary antibodies to detect primary antibodies in methods such as western blot, immunohistochemistry, and immunofluorescence staining for microscopy or flow cytometry. Recombinant production provides highly reliable anti-immunoglobulin antibodies with the highest possible batch-to-batch reproducibility. In addition, recombinant antibody technology enables antibody engineering to open up new experimental possibilities.
We also offer secondary antibodies against human or other primate antibodies. If you are looking for another species or target, please contact us.
Antibody Name [Clone] | Species Reactivity | Catalog Number |
Anti-Rat IgG [OX-59] | Rat | Ab00588 |
Anti-Rat antibody kappa light chains [OX-12] | Rat | Ab00581 |
Anti-Rabbit IgG [A10B] | Rabbit | Ab03007 |
Anti-Mouse antibody kappa light chain [OX-20] | Mouse | Ab00583 |
Anti-loggerhead IgY spliced chain [LH1] | Loggerhead turtle; Green sea turtle; Kemp’s ridley turtle | Ab02499 |
Anti-loggehead IgY heavy chain [LH-12-4] | Sea turtles | Ab02497 |
Anti-lambda light chain [8-H9] | Ferret (Mustela putorius furo) | Ab02372 |
Anti-lambda light chain [6-H5] | Ferret (Mustela putorius furo) | Ab02371 |
Anti-lambda light chain [4-D11] | Ferret (Mustela putorius furo) | Ab02370 |
Anti-kappa light chain [4-B10] | Ferret (Mustela putorius furo) | Ab02368 |
Anti-immunoglobulin [6-B5] | Ferret (Mustela putorius furo) | Ab02373 |
Anti-IgNAR [GA8] | Elasmobranch | Ab01553 |
Anti-IgM (Igh-Cb and related haplotypes) [AF6-78.25.4] | Mouse | Ab02574 |
Anti-IgG3 Fc [TP924] | Mouse; Rabbit | Ab01460 |
Anti-IgG2b Fab [TP984] | Mouse | Ab01459 |
Anti-IgG2b Fab [TP979] | Mouse; Guinea pig | Ab01458 |
Anti-IgG2a/3 Fc [TP929] | Mouse; Rabbit (weak) | Ab01461 |
Anti-IgG2a/2b Fc [TP925] | Mouse | Ab01457 |
Anti-IgG2a Fc [TP923] | Mouse | Ab01455 |
Anti-IgG2a Fc [TP922] | Mouse | Ab01454 |
Anti-IgG2a Fc [TP1129] | Mouse | Ab01453 |
Anti-IgG2a (hinge) [TP926] | Mouse | Ab01456 |
Anti-IgG1/2a/2b Fab (k) [TP1106] | Mouse | Ab01452 |
Anti-IgG1/2a Fab (k) [TP890] | Mouse | Ab01451 |
Anti-IgG1/2a Fab (k) [TP889] | Mouse | Ab01450 |
Anti-IgG1/2a Fab (k) [TP888] | Mouse | Ab01449 |
Anti-IgG1/2a Fab (k) [TP887] | Mouse | Ab01448 |
Anti-IgG1 Fc [TP895] | Mouse | Ab01445 |
Anti-IgG1 Fc [TP894] | Mouse | Ab01444 |
Anti-IgG1 Fc [TP884] | Mouse; Rat (weak) | Ab01443 |
Anti-IgG1 Fc [TP883] | Mouse; Rat; Human (weak) | Ab01442 |
Anti-IgG1 Fc [TP882] | Mouse; Rat | Ab01441 |
Anti-IgG1 Fc [TP881] | Mouse; Rat (weak) | Ab01440 |
Anti-IgG1 Fc [TP879] | Mouse; Rat | Ab01438 |
Anti-IgG1 Fc [TP878] | Mouse | Ab01437 |
Anti-IgG1 Fc [TP1107] | Mouse; Rat; Human (weak) | Ab01436 |
Anti-IgG1 Fc [TP1104] | Mouse | Ab01439 |
Anti-IgG1 Fab (k+l) [TP886] | Mouse | Ab01447 |
Anti-IgG1 (hinge) [TP885] | Mouse; Rat | Ab01446 |
Anti-IgG [GT175] | Goat | Ab01020 |
Anti-IgE [R1E4] | Mouse | Ab01115 |
Anti-IgE [mAbA9] | Mouse | Ab01158 |
Anti-IgE [D9#3116] | Dog | Ab01391 |
Anti-IgD (Igh-Ca haplotype) [AMS9- 9.1.1.1] | Mouse | Ab02573 |
Anti-Fc [TP897] | Rabbit; Guinea pig; Human (weak) | Ab01432 |
Anti-Fab [TP896] | Rabbit | Ab01431 |
Anti-Fab (lambda) [TP1014] | Mouse; Rat; Rabbit (weak) | Ab01435 |
Anti-Fab (kappa) [TP975] | Mouse | Ab01434 |
Anti-Fab (kappa) [TP1170] | Mouse | Ab01433 |
Anti-antibody heavy chain [6-B7] | Ferret (Mustela putorius furo) | Ab02374 |
Anti-antibody heavy chain [11-E3] | Ferret (Mustela putorius furo) | Ab02375 |
Anti-kappa light chain [4-E3] | Ferret (Mustela putorius furo) | Ab02369 |
Anti-chicken IgY [IgY 176] | Chicken | Ab02049 |
Anti-loggerhead IgY light chain [LH9] | Sea turtles | Ab02498 |
Anti-IgM [1.14] | Trout | Ab02046 |
IgE is an often overlooked antibody isotype, but it plays a critical role in allergic reactions and certain autoimmune diseases. To advance related research and diagnostics, Absolute Antibody has used recombinant antibody technology to develop highly reproducible IgE proteins in a wide range of species. These Fc-only proteins can be used for a variety of applications:
We now offer IgE Fc domain proteins in a variety of species. We started with the common models, human and mouse, and have recently expanded our catalog to include animals such as dog, cat and horse. The new species are ideal for veterinary research and diagnostic assay design.
The IgE Fc domain proteins react with species-specific anti-IgE antibodies, with no cross-reactivity observed (see ELISA data below).
Currently available IgE Fc domain proteins are listed below. We also offer immunoglobin Fc domains in other subtypes, including IgG1, IgG2A, IgA and IgM; you can view our full list of Ig Fc domains here. For more information or to place an order, please contact us.
Interested in using these Fc proteins to create antigen-specific antibodies? Choose a target from our extensive catalog, or provide your own antibody, and we’ll do the rest. Check out our selection of anti-allergen antibodies, and contact us to discuss your project!
Catalog Number | Product Name |
Pr00104-14.5 | Recombinant Human IgE-Fc domain |
Pr00107-20.5 | Recombinant Mouse IgE-Fc domain |
Pr00344-39.5 | Recombinant Dog IgE-Fc domain |
Pr00343-38.5 | Recombinant Cat IgE-Fc domain |
Pr00345-40.5 | Recombinant Horse IgE-Fc domain |
Fc fusion proteins (also known as Fc chimeric fusion proteins, Fc-Igs, Ig-based chimeric fusion proteins and Fc-tag proteins) are composed of the Fc domain of IgG genetically linked to a peptide or protein of interest. Fc fusion proteins have become valuable reagents for in vivo and in vitro research.
Examples of Fc-fused binding partners include, but are not limited to, single peptides, ligands activated upon cell-surface receptor binding, signaling molecules, extracellular domains of receptors activated upon dimerization and bait proteins used to identify binding partners in protein microarrays.
One of the most valuable characteristics conferred by the Fc domain in vivo is the dramatic prolonging of the plasma half-life (t1/2) of the protein of interest, which for biotherapeutic drugs can result in improved therapeutic efficacy, an attribute that has made Fc fusion proteins attractive biotherapeutic agents.
n vitro applications of Fc fusion proteins include, among others, immunohistochemistry (IHC), flow cytometry (FC), protein binding assays and use as microarray baits. In these applications, the Fc domain behaves as a supporting module to which proteins can be attached while retaining their native biological activity. The Fc domain can also improve the in vivo and in vitro solubility and stability of some binding partners.
Absolute Antibody offer a diverse array of recombinant Fc fusion proteins with a range of species-specific and genetically engineered Fc domains such as Fc Silent™.
For further information or for bulk and custom orders, do not hesitate to contact us.
Catalog Number | Product Name | Recombinant Protein Species | Immunoglobulin Fc domain Isotype and Species |
Pr00246-10.9 | Recombinant human NR3L1 Fc-Fusion Protein | Human | Human IgG1 |
Pr00245-10.9 | Recombinant human FCRL6 Fc-Fusion Protein | Human | Human IgG1 |
Pr00244-10.9 | Recombinant humanBY55 Fc-Fusion Protein | Human | Human IgG1 |
Pr00243-10.9 | Recombinant human TIMG2 Fc-Fusion Protein | Human | Human IgG1 |
Pr00242-10.9 | Recombinant human TMM81 Fc-Fusion Protein | Human | Human IgG1 |
Pr00241-10.9 | Recombinant human NCAM1 Fc-Fusion Protein | Human | Human IgG1 |
Pr00240-10.9 | Recombinant human LINGO2 Fc-Fusion Protein | Human | Human IgG1 |
Pr00239-10.9 | Recombinant human LAIR2 Fc-Fusion Protein | Human | Human IgG1 |
Pr00238-10.9 | Recombinant human LAIR1 Fc-Fusion Protein | Human | Human IgG1 |
Pr00237-10.9 | Recombinant human HAVCR1 Fc-Fusion Protein | Human | Human IgG1 |
Pr00236-10.9 | Recombinant human CADM1 Fc-Fusion Protein | Human | Human IgG1 |
Pr00235-10.9 | Recombinant human AMIGO3 Fc-Fusion Protein | Human | Human IgG1 |
Pr00234-10.9 | Recombinant human CD70 Fc-Fusion Protein | Human | Human IgG1 |
Pr00233-1.9 | Recombinant mouse 4-1BB Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00232-1.28 | Recombinant mouse TL1A Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00231-1.9 | Recombinant mouse CD155 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00230-1.9 | Recombinant mouse CD96 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00228-1.9 | Recombinant mouse TIM-3 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00227-1.9 | Recombinant mouse TIM-1 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00226-1.9 | Recombinant mouse CD86 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00225-1.9 | Recombinant mouse CD80 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00224-1.9 | Recombinant mouse BTLA Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00223-1.9 | Recombinant mouse HVEM Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00206 | Recombinant mouse CD52-Fc Fusion Protein | Mouse | Mouse IgG1 |
Pr00188-10.9 | Recombinant human SLAF6 Fc-Fusion Protein | Human | Human IgG1 |
Pr00187-10.9 | Recombinant human TNR4 Fc-Fusion Protein | Human | Human IgG1 |
Pr00186-10.28 | Recombinant human CD69 Fc-Fusion Protein | Human | Human IgG1 |
Pr00185-10.9 | Recombinant human SEM4D Fc-Fusion Protein | Human | Human IgG1 |
Pr00183-10.9 | Recombinant human NKG2-F Fc-Fusion Protein | Human | Human IgG1 |
Pr00182-10.9 | Recombinant human TNR9 Fc-Fusion Protein | Human | Human IgG1 |
Pr00181-10.9 | Recombinant human CEACAM1 Fc-Fusion Protein | Human | Human IgG1 |
Pr00180-10.9 | Recombinant human SLAF7 Fc-Fusion Protein | Human | Human IgG1 |
Pr00179-10.9 | Recombinant human CD27 Fc-Fusion Protein | Human | Human IgG1 |
Pr00178-10.9 | Recombinant human PTPRC Fc-Fusion Protein | Human | Human IgG1 |
Pr00164-1.9 | Recombinant mouse VISTA Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00163-1.9 | Recombinant mouse TIGIT Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00162-1.9 | Recombinant mouse Lag3 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00161-1.28 | Recombinant mouse CD70 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00160-1.9 | Recombinant mouse CD27 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00159-1.28 | Recombinant mouse 4-1BBL Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00158-1.9 | Recombinant mouse B7-H3 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00157-1.9 | Recombinant mouse ICOSL Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00156-1.9 | Recombinant mouse PDL2 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00155-1.9 | Recombinant mouse CTLA4 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00154-1.9 | Recombinant mouse OX40 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00153-1.9 | Recombinant mouse ICOS Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00152-1.9 | Recombinant mouse PD-1 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00136 | Recombinant human CTLA-4 Fc-Fusion Protein (Abatacept) | Human | Human IgG1 |
Pr00135 | Recombinant human TNFR1B Fc-Fusion Protein (Etanercept) | Human | Human IgG1 |
Pr00128-10.28 | Recombinant human NKG2E Fc-Fusion Protein | Human | Human IgG1 |
Pr00127-10.9 | Recombinant human NCTR1 Fc-Fusion Protein | Human | Human IgG1 |
Pr00126-10.9 | Recombinant human NCTR3 Fc-Fusion Protein | Human | Human IgG1 |
Pr00125-10.28 | Recombinant human NKG2D Fc-Fusion Protein | Human | Human IgG1 |
Pr00124-10.9 | Recombinant human CD96 Fc-Fusion Protein | Human | Human IgG1 |
Pr00123-10.9 | Recombinant human CD226 Fc-Fusion Protein | Human | Human IgG1 |
Pr00122-10.9 | Recombinant human TIGIT Fc-Fusion Protein | Human | Human IgG1 |
Pr00117-10.9 | Recombinant human EGFR Fc-Fusion Protein | Human | Human IgG1 |
Pr00113-1.9 | Recombinant mouse CD47 (C33 to G mutation) Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00112-1.9 | Recombinant mouse PDL1 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00111-1.9 | Recombinant mouse TNFR1 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00109-1.9 | Recombinant mouse IL2 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00103-10.13 | Recombinant Human CTLA-4 Fc Silent™-Fusion Protein | Human | Human IgG1 Fc Silent™ mutations in the Fc |
Pr00103-10.9 | Recombinant Human CTLA-4 Fc-Fusion Protein | Human | Human IgG1 |
Pr00439 | Recombinant Human ACE2-IgG Fc (LALA)-Fusion Protein | Human | Human IgG1 (with silencing LALA mutations) |
Pr00441 | Recombinant Human ACE2-NN-IgG Fc (LALA)-Fusion Protein | Human | Human IgG1 (with silencing LALA mutations) |
Pr00251 | Recombinant S1-camel Fc-Fusion Protein | MERS | Camel |
Pr00118-1.9 | Recombinant IL-13 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00510-1.9 | Recombinant CD40 Fc-Fusion Protein | Mouse | Mouse IgG1 |
Pr00511-10.9 | Recombinant CD40 Fc-Fusion Protein | Human | Human IgG1 |
Pr00512-201.9 | Recombinant CD40 Fc-Fusion Protein | Dog | Dog IgG2 |
Pr00513-201.9 | Recombinant PD1 Fc-Fusion Protein | Dog | Dog IgG2 |
Pr00514-201.9 | Recombinant PDL1 Fc-Fusion Protein | Dog | Dog IgG2 |
Pr00515-201.9 | Recombinant ICOS Fc-Fusion Protein | Dog | Dog IgG2 |
Pr00516-201.9 | Recombinant CTLA4 Fc-Fusion Protein | Dog | Dog IgG2 |
Figure 1. A schematic representation of the structure of four immunoglobulin (Ig) classes or isotypes and their Fc domains. The Ig Fc domain does not bind antigen- see Antibody Isotypes and Subtypes and Antibody Effector Functions for a detailed account on structure and function of antibodies.
We offer a range of isotype- and species-specific Ig Fc domains – please see the table below.
Recombinant Ig Fc domains are recommended as:
For further information or to request a species or isotype not yet shown, please contact us.
Catalog Number | Product Name |
Pr00100-10.5 | Recombinant Human IgG1-Fc domain |
Pr00101-1.5 | Recombinant Mouse IgG1-Fc domain |
Pr00102-2.5 | Recombinant Mouse IgG2A-Fc domain |
Pr00104-14.5 | Recombinant Human IgE-Fc domain |
Pr00105-16.5 | Recombinant Human IgA-Fc domain |
Pr00107-20.5 | Recombinant Mouse IgE-Fc domain |
Pr00108-15.5 | Recombinant Human LMW IgM-Fc domain (monomeric) |
Pr00343-38.5 | Recombinant Cat IgE-Fc domain |
Pr00344-39.5 | Recombinant Dog IgE-Fc domain |
Pr00345-40.5 | Recombinant Horse IgE-Fc domain |
Absolute Antibody’s Multi-Tag control protein (Pr00106) and Multi-Tag control protein 2 (Pr00565) are genetically engineered synthetic fusion proteins composed of commonly used epitope tags fused together using flexible linkers (Figure 1 and 2). These Multi-Tag synthetic fusion proteins can be used as a positive control in western/dot blots and ELISAs.
You can also check out our epitope tags page for our full range of recombinant and chimeric anti-epitope tag monoclonal antibodies. For further information on our Multi-Tag control proteins or any of our products, contact us and we will be happy to help.
Figure 1: A schematic representation of the Absolute Antibody’s Multi-Tag control protein (Pr00106), composed of 17 commonly used epitope tags shown in sequence from N- to C-terminal.
Figure 2: A schematic representation of the Absolute Antibody’s Multi-Tag control protein 2 (Pr00565), composed of 12 commonly used epitope tags shown in sequence from N- to C-terminal.
Multi-Tag control protein (Pr00106) | Multi-Tag control protein 2 (Pr00565) | ||
Thioredoxin (Trx) tag | SDKIIHLTDDSFDTDVLKADGAILVDF
WAEWCGPCKMIAPILDEIADEYQGK LTVAKLNIDQNPGTAPKYGIRGIPTLLL FKNGEVAATKVGALSKGQLKEFLDAN LA |
MBP tag | MKIEEGKLVIWINGDKGYNGLAEVGKKFE
KDTGIKVTVEHPDKLEEKFPQVAATGDGP DIIFWAHDRFGGYAQSGLLAEITPDKAFQ DKLYPFTWDAVRYNGKLIAYPIAVEALSLI YNKDLLPNPPKTWEEIPALDKELKAKGKS ALMFNLQEPYFTWPLIAADGGYAFKYEN GKYDIKDVGVDNAGAKAGLTFLVDLIKNK HMNADTDYSIAEAAFNKGETAMTINGP WAWSNIDTSKVNYGVTVLPTFKGQPSKP FVGVLSAGINAASPNKELAKEFLENYLLTD EGLEAVNKDKPLGAVALKSYEEELAKDPRI AATMENAQKGEIMPNIPQMSAFWYAVR TAVINAASGRQTVDEALKDAQTNSSSNN NNNNNNNNLGIEGR |
T7 tag | CMASMTGGQQMG | GCN4 tag | HLENEVARLKK |
HSV tag | QPELAPEDPEDC | MAP-tag | GDGMVPPGIEDKIT |
VSV-g tag | YTDIEMNRLGKG | Protein C tag | EDQVDPRLIDGK |
Glu-Glu tag | CEEEEYMPME | Rap-tag | GDDMVNPGLEDRIEC |
V5-tag | GKPIPNPLLGLDST | Rho-tag | TETSQVAPA |
E-tag | GAPVPYPDPLEPR | Alpha-tag | SRLEEELRRRLTE |
HA tag | YPYDVPDYAC | Rim-tag | PLHPRTAGASR |
FLAG tag | DYKDDDDK | Softag | SLAELLNAGLGGS |
GST tag
|
PILGYWKIKGLVQPTRLLLEYLEEKYEE
HLYERDEGDKWRNKKFELGLEFPNLP YYIDGDVKLTQSMAIIRYIADKHNML GGCPKERAEISMLEGAVLDIRYGVSRI AYSKDFETLKVDFLSKLPEMLKMFED RLCHKTYLNGDHVTHPDFMLYDALD VVLYMDPMCLDAFPKLVCFKKRIEAI PQIDKYLKSSKYIAWPLQGWQATFG GGDHPPKSDLV |
Strep tag | WSHPQFEK |
Myc tag | EQKLISEEDLC | His tag | HHHHHH |
S-tag | KETAAAKFERQHMDS | Pep tag | AVERYLKDQQLLGIW |
KT3 tag | KPPTPPPEPET | ||
E2-tag | GVSSTSSDFRDR | ||
AU1 tag | DTYRYI | ||
AU5 tag | TDFYLK | ||
His tag | HHHHHH |
Catalog Number | Product Name |
Pr00106 | Multi-Tag Control Protein |
Pr00565 | Multi-Tag Control Protein 2 |
Free antibody light chains are important diagnostic markers for a range of disorders including amyloidosis, various myelomas and lymphomas. Absolute levels as well as imbalances in the ratio of free kappa and lambda chains are used as diagnostic and prognostic markers.
The recombinant expression platform used by Absolute Antibody allows the direct expression of free antibody light chains, overcoming the common problems faced in purifying these proteins. Our serum-free culturing system and affinity purification result in ultra-pure product that may be used as calibrators and positive controls for diagnostic assays.
We offer both lambda and kappa light chains.
For larger quantities or more information, please contact us and we will be happy to help you.
Coomassie-stained SDS-PAGE gel of human recombinant free lambda (left) and kappa (right) light chains. Starting from the tissue culture supernatant, a single purification step was perfomed to enrich for recombinant free light chains, both as monomer and dimer (at around 28 and 50 kDa, respectively).
Catalog Number | Product Name |
Pr00115 | Recombinant Human Free Kappa Light Chain |
Pr00116 | Recombinant Human Free Lambda Light Chain |
Good, validated antibodies are highly valuable, but hybridomas are easily lost. Storage accidents, genetic drift or contamination can threaten the security of your antibody.
One solution is to sequence your antibody to enable recombinant production. Sequencing an antibody is vital when obtaining intellectual property rights for your sequence, and expands your antibody’s potential with antibody engineering options.
Absolute Antibody offers a quick and professional hybridoma sequencing service, also known as antibody sequencing. Hybridoma sequencing is the sequencing of the cDNA encoding the variable heavy (VH) and variable light (VL) domains of your hybridoma cell line.
Sequencing the antibody genes of your hybridoma offers many advantages:
Contact us to receive a quote or to discuss your requirements in more detail.
Our method – The mRNA transcriptome is obtained from the hybridoma and random hexamers are used to generate a cDNA library. This is fragmented, and undergoes paired-end sequencing. The sequencing reads are assembled into contigs, from which antibody transcripts are identified based on homology.
At Absolute Antibody we perform high throughput (NGS) hybridoma sequencing. In 4-6 weeks, we deliver you all VH and VL sequences as well as a full report characterizing your hybridoma’s sequences and any heterogenicity or other antibody isotypes that might be present.
Even if a hybridoma is contaminated or unproductive, we could be able to save your antibody for recombinant expression. Review our collection of hybridoma sequencing case studies to learn how our unique NGS method can help overcome such obstacles to antibody production. Contact us about your project to see if we can help.
If you want to sequence a large hybridoma collection or your entire antibody catalog, contact us to discuss our bulk hybridoma sequencing options.
If you want to sequence antibody directly from purified protein, read about our protein sequencing service.
We also provide follow on services – read our antibody engineering and antibody expression pages for more information.
We provide instructions for shipping hybridoma cell lines in your order quote. You may request a free SeqPack™ Hybridoma Preservation Kit if you do not wish to ship using dry ice.
Please contact us to learn more about our hybridoma sequencing and request an order quote. Bulk discounts may apply.
There are many monoclonal antibodies for which the hybridoma cell line is unavailable. To complement our hybridoma sequencing service, we are also offering a de novo antibody protein sequencing service.
By combining mass spectrometry with high accuracy de novo peptide sequencing and assembly of overlapping peptides, the amino acid sequences of the variable domains are determined.
We guarantee to deliver a functional antibody sequence along with a comprehensive sequencing report with full sequence coverage. In combination with our transient expression service, we can sequence an antibody and deliver recombinant versions in as little as 9 weeks.
De novo sequencing workflow: The antibody is digested using multiple enzymes. On each digest LC-MS-MS is performed and peptides predicted de novo. Using proprietary software, overlapping peptides are assembled into a full coverage protein sequence.
Customer Provides | Mass Spectrometric Sequencing | Antibody Expression | Timeline | Deliverables |
Monoclonal antibody, >0.1 mg, 95% pure |
|
|
9 weeks |
|
Polyclonal antibodies are widely used reagents across research and diagnostics. They are generated by immunizing animals with an immunogen and harvesting the animals’ blood to obtain immunoreactive serum. While polyclonal antibodies offer a range of advantages such as excellent performance across different methods, they suffer from high batch-to-batch variability and require the continued use of animals for their production.
Turning a polyclonal antibody into an infinitely reproducible recombinant antibody has been described as the Holy Grail of reagent antibody technology with far-reaching potential. Now, advances in antibody protein sequencing technology have made it possible to sequence a polyclonal antibody protein sample and obtain highly functional recombinant monoclonal antibodies from the sequence.
Absolute Antibody has partnered with leading industry innovators, including Rapid Novor and Abterra Bio, to enable the production of animal-free polyclonal reagents that are both reproducible and in unlimited supply. Our partners have pioneered the cutting-edge sequencing technology, while Absolute Antibody provides the antibody expression expertise to recombinantly produce monoclonal antibodies from the sequences. We also offer confirmation of binding compared to the original polyclonal antibody, as well as the expression of multiple clones to create an antibody mixture.
We partnered with Rapid Novor to sequence and express monoclonal antibodies from a polyclonal goat antibody sample
Reporting the de novo sequencing of monoclonal antibodies from a polyclonal goat antibody sample by mass spectrometry, followed by recombinant expression and testing. To our knowledge, this is the first report of a successful conversion of a goat polyclonal to a monoclonal using just antibody protein as a template.
We believe that with continual validation, polyclonal antibody sequencing will have a profound impact on the research reagents and diagnostics industry. It also shows great potential for the development of therapeutics from existing polyclonal antibodies. In addition to guaranteeing long-term reproducibility, sequencing a polyclonal antibody enables researchers to extend the usefulness of their original antibody through engineering. Our antibody engineering services allow for a wealth of possibilities, including species and isotype switching, or the creation of novel formats such as high avidity fragments or multispecific antibodies.
If you have a polyclonal antibody you would like to immortalize into a precisely defined and reproducible reagent, please contact us to learn more about our polyclonal antibody sequencing service. The service is ideal for immortalizing challenging immunizations and researchers interested in pushing the boundaries of recombinant antibody technology.
At Absolute Antibody we have developed a proprietary cloning system to enable rapid reformatting of antibodies into almost any format. Our antibody engineering services include chimerization, humanization, isotype switching and the manufacturing of recombinant antibody fragments and bispecific antibodies. For more information about any of these services, please follow the links, download our Guide to Antibody Engineering white paper, or get in touch – we’re happy to help.
The following species, isotypes and formats are currently available at Absolute Antibody with more coming soon. For more details about the unique formats we can custom engineer for clients, check out our Periodic Table of Antibodies.
Antibody format | Human | Mouse | Rat | Hamster | Rabbit | Goat | Rhesus | Cyno | Sheep | Dog | Pig | Ferret |
IgG | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ |
IgA | ✓ | ✓ | ✓ | ✓ | ||||||||
IgE | ✓ | ✓ | ✓ | |||||||||
IgM | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ||||||
Fc domains | ✓ | ✓ | ||||||||||
Fabs | ✓ | ✓ | ||||||||||
Fab2 | ✓ | ✓ | ||||||||||
Fc fusions | ✓ | ✓ | ✓ | |||||||||
Bispecifics | ✓ | ✓ |
If you require antibodies of a species not listed, please do not hesitate to ask. Currently we have antibody sequences available for a large number of animals ranging from pig, sheep, horse, dog, chicken, fish, platypus and a whole range of non-human primates. Moreover, our in-house experts are able to determine antibody sequences from most genomes (even if only partial assemblies are available). If you are looking for something very unusual, please contact us.
We offer an antibody chimerization service which enables you to create a chimeric antibody, consisting of the original variable domains from your antibody with the constant domains from a different species, for almost any mammalian species. In particular, we offer chimerization of human, mouse, rat, rabbit and hamster IgG with other species and isotypes available by request. For more information, please visit our dedicated page on chimeric antibodies or contact us.
We offer a royalty-free antibody humanization service. For more information, please see our dedicated page on antibody humanization or contact us.
Our isotype switching service (also known as class switching) allows you to alter the isotype or subtype of any antibody. This can be used to alter the in vivo effector function and stability of an antibody. Equally, some antibody subtypes are prone to aggregation. Switching the isotype/subtype can help overcome this. Or perhaps you would like to convert your IgG to an IgM for increased avidity? We can offer all these things and more. For more information or to request a quote, contact us.
In certain situations antibody fragments offer an ideal alternative to full-length antibodies. Our proprietary recombinant expression and antibody engineering platform enables us to convert any antibody into a fragment, such as a single chain Fv (scFv), Fab or Fab2, followed by expression and purification at any scale. For more information, please visit our dedicated page on antibody fragments or contact us. For a general information guide on the types and uses of fragments, please see our Absolute Antibody resource page on antibody fragments.
Absolute Antibody offers a bispecific antibody service. We can reformat any pair of antibodies into an IgG-scFv format (i.e. an IgG with a scFv fused to the C-terminus of the IgG). This results in a bispecific bivalent antibody format capable of binding two antigens simultaneously. For more information, see our dedicated page on bispecific and trispecific antibodies or to request a quote please contact us.
Absolute Antibody can engineer the Fc domain of your antibody to mediate effector function or extend the plasma half-life. For example, we can abolish Fc domain binding to FcγR using our Fc Silent™ mutation or mAbsolve’s STR mutations, as well as extend or shorten the plasma half-life of your IgG antibody by introducing mutations in the Fc domain.
Below is a selection of the formats we have engineered for our customers. Contact us with your ideas – we’ll see what we can do! You can explore our interactive Periodic Table of Antibodies
Our antibody expression platforms rapidly produce high-quality, animal-free recombinant antibodies at milligram-to-gram scale in HEK or CHO cells. Our serum-free mammalian transient expression system offers a faster, more affordable alternative to stable cell line generation, and we’ve used it to manufacture recombinant antibodies in any species, isotype or format with high purity and low endotoxin levels.
Depending on your antibody expression needs, we are a reliable outsourcing solution for antibody production, or a true consultative partner for developing the best possible engineered antibody. All production occurs at our ISO 9001:2015-certified manufacturing facility, which enables high-throughput capacity and the ability to scale up to multi-gram quantities within weeks.
We have experience manufacturing antibodies for clients worldwide, including pharmaceutical and biotechnology companies, diagnostic assay developers and academic researchers. We have produced more than 21,000 different recombinant antibodies, making 865 grams of protein in total and expanding our all-recombinant reagents catalog to more than 13,500 antibodies. As illustrated by our Periodic Table of Antibodies, we’ve manufactured more than 180 different antibody formats to date, including multispecific antibodies, fragments and Fc fusion proteins.
Our antibody expression services are all royalty-free and customizable to your needs. We can start from an electronic antibody sequence, hybridoma cell line or purified antibody protein. In addition, your project will be supported by scientific staff with deep expertise in antibody development, a dedicated project manager, and a global customer service team across North America, Europe and Asia.
Read about all our different antibody expression services below. To learn more, contact us.
Our HEXpress™ service produces milligram-to-gram quantities of recombinant antibodies in HEK cells with high purity and low endotoxin levels. This service provides a faster, more affordable alternative to stable cell line generation, with proven expression of antibodies in any species, isotype or format.
Our CHXpress™ service enables serum-free mammalian transient expression in CHO cells to better serve clients through their full antibody development. This service is particularly useful for bridging the gap to stable CHO production, or for tackling challenging constructs.
Our FleXpress™ service allows clients to rapidly express large numbers of IgG antibodies at 80 ml scale using our proven recombinant antibody technology. This service is particularly useful for early-stage pilot studies on a group of therapeutic antibody candidates, as well as converting a monoclonal antibody portfolio from hybridomas to recombinant production.