This product selects the subtype A (FAM) and subtype B (HEX) regions of respiratory syncytial virus and designs two sets of primers and fluorescent probes. The two sets of primers and probes can specifically bind to the tanget sequences. When the RT-PCR amplification reaction is performed, the fluorescent signal(s) can be detected by a full-automatic fluorescent PCR detector to realizereal-time online monitoring of the RT-PCR reaction. In order to control the entireextraction and detection process, human gene was act as a non-competitive internal control during the extraction and detection process.
• Good specificity
No cross reaction with a variety of common respiratory infection pathogens such as Pertussis bacillus, Moraxella catarrh, Influenza A H1N1 virus, Influenza B virus, Adenovirus type 7, Mycoplasma pneumoniae, Streptococcus pneumoniae, etc.
• Excellent anti-interference ability
The samples contained endogenous inhibitors (such as blood, mucin and nasal secretions) and exogenous inhibitors (such as common drugs for treating colds or other similar symptoms), and no significant influence was observed on the test results.
• Simple operation
One-step RT-QPCR, complete closed tube amplification and detection, to prevent aerosol pollution. The detection report can be completed in 60 minutes.
-20 ± 5 ℃ avoid light
| Cat# | Product Name | Packing size |
| BSJ05S1 | Respiratory Syncytial Virus Type A / Type B Nucleic Acid Detection Kit (Fluorescent RT-PCR) | 24T |
| BSJ05M1 | Respiratory Syncytial Virus Type A / Type B Nucleic Acid Detection Kit (Fluorescent RT-PCR) | 48T |
| BSJ05L1 | Respiratory Syncytial Virus Type A / Type B Nucleic Acid Detection Kit (Fluorescent RT-PCR) | 96T |