SARS-CoV-2 and Influenza Viruses A/B Rapid Test Cassette is based on the principle of colloidal gold immunochromatography sandwich method, this kit is used to detect SARS-CoV-2 nucleoprotein antigen and Influenza A/B virus antigens in human nasal swabs. After dripping the sample, the sample moves upward through the action of capillary. if there is SARS-CoV-2 nucleoprotein antigen or Influenza A/B virus antigens in the sample, it will combine with the colloidal gold labeled SARS-CoV-2 antibody and Influenza A/B virus antibody fixed on the gold pad to form an immune complex, then the immune complex is captured on the membrane by the pre-coated SARS-CoV-2 nucleoprotein monoclonal antibody or Influenza A/B virus antibody, and a visible red line will appear in the detection line area. A red line will always appear in the area of the quality control line, indicating that the testing process is correct.
Cat. No: CG9092(S)-AN-D
SARS-CoV-2 and Influenza Viruses A/B Rapid Test Cassette( personal test)
Test procedure
This test is suitable for people of all ages. The recommend operators are aging from 14 to 90 years. Children under 14 years of age and illiterate persons should be tested by an adult supervisor. Do not continue the test if the child feels any pain.
Content of The Test Kit
Serial number Components Ingredient 1 Test cassette Nitrocellulose membrane, SARS-CoV-2 monoclonal antibody (fixed on nitrocellulose membrane), SARS-CoV-2 monoclonal antibody (fixed on fiberglass), Influenza A virus monoclonal antibody (fixed on nitrocellulose membrane), Influenza A virus monoclonal antibody (fixed on fiberglass), Influenza B virus monoclonal antibody (fixed on nitrocellulose membrane), Influenza B virus monoclonal antibody (fixed on fiberglass), goat anti-rabbit IgG, rabbit IgG, Goat anti-mouse IgG 2 Extraction Tube (Contains extraction reagent) Tris、Surfactant 3 Biohazard Disposal Bag / 4 Sterilized Swab / 5 Instruction for use /
Limitations:
1.This reagent is a qualitative in vitro diagnostic reagent for auxiliary diagnosis. The test results of this kit are for clinical reference only, and should not be used as the only basis for clinical diagnosis. It should be judged comprehensively according to clinical symptoms and other detection indexes. 2.This reagent is only used for qualitative detection of SARS-CoV-2 antigen and influenza A/B virus antigen in human nasal swabs. 3.The positive results only indicate the possible existence of SARS-CoV-2 antigen or influenza A/B virus antigen, which can not be used as the only criterion for SARS-CoV-2 or influenza A/B virus infection. 4.The negative result can not completely rule out the possibility of SARSCoV-2 or influenza A/B virus infection, it may be that SARS-CoV-2 antigen or influenza A/B virus antigen level is too low to be detected by this kit, or other reasons lead to false negative results. 5.Inconsistent or incorrect results may be caused by improper technical or step operation, contamination of samples, and the presence of drugs that interfere with the detection. 6.The methods of sample collection and processing have a great impact on virus detection, and improper operation may lead to wrong results. The samples treated by heat inactivation and guanidine salt may cause inaccurate test results.
