Catalogue Number: MD04902-NZY
Manufacturer: | NZYTech |
Type: | qPCR Kits |
Shipping Condition: | Blue Ice |
Storage Condition: | -70°C |
Unit(s): | 4 x 96 reactions |
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Application: | RT-PCR, RT-qPCR |
Description: NZYTech's COVID-19, Flu A/B, RSV Multiplex One-Step RT-qPCR Kit, IVD provides the complete set of reagents and probes to qualitatively detect the SARS-CoV-2, RSV and/or Influenza genomes, through common real-time PCR platforms. SARS-CoV-2 is identified by detecting RT-qPCR targets located in RdRp and N genes. In contrast, Influenza A and Influenza B viruses are detected through the amplification of targets located in M1 and NS2 genes, respectively. RSV virus is detected through the amplification of target located in L gene and the human ribonuclease P (RNase P, RP) gene. In case the IFU is not available in your official country language, please contact us - info@nzytech.com so that we can proceed with the translation. Please see languages available below. High Sensitivity: Early virus detection and diagnosis, detects as low as 250 copies/mL of SARS-CoV-2, 375 copies/mL of Influenza A, 375 copies/mL of Influenza B viral RNA and 375 copies/mL of RSV viral RNA (LoD) sample. Precision: Coefficient of variation (CV) < 2.20% for SARS-CoV-2; Coefficient of variation (CV) < 3.34% for Influenza A; Coefficient of variation (CV) < 2.56% for Influenza B, Coefficient of variation (CV) < 2.85% for RSV allowing reproducible test results High Throughput: Up to 93 clinical samples (96-well plate); up to 381 clinical samples (384-well plate) High Specificity: Proven by in silico analysis as well as wet lab testing Flexibility: Assay validated on widely used qPCR instruments including Applied Biosystem® 7500 FAST, Applied Biosystem® QuantStudio 5, Bio-Rad® CFX96 Fast Time: < 1h from nucleic acid extraction to results. Minimal Sample Input: As low as 2 µL sample needed. Find the IFU for your product batch
NZYTech's COVID-19, Flu A/B, RSV Multiplex One-Step RT-qPCR Kit, IVD provides the complete set of reagents and probes to qualitatively detect the SARS-CoV-2, RSV and/or Influenza genomes, through common real-time PCR platforms.