Product Details:
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Total Accuracy: | 98.02% | Specimen: | Saliva |
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Test Time: | <15 Min | Quanlity Guarantee Period: | 18 Months |
Storage Condition: | 2℃-30℃ | Format: | Cassette |
High Light: | Cassette One Step Rapid Test Kit,98.02% one step rapid test kit,ISO 13485 saliva rtk test kit |
SARS-CoV-2 Antigen Saliva Rapid Test Kit (Immunochromatography)
Intend Use
This rapid test kit is intedded for the qualitative detection of SARS-CoV-2 antigen in saliva sample wihch also can be used to detect saliva sample from novel coronavirus suspected person with symptoms within 9 days. The test result of antigen test can be used for early triage and rapid management of suspected popu;ations, but it cannot be used as diagnosis basis of SARS-CoV-2 infection and as the sole basis for treatment or patient management decidions. Fuether nucleis acid detection should be carried out for suspected population whose antigen test result is positive or negative
Product Details
Item | Value |
Model Number | LX-401603 |
Type | 20 Test |
Warranty | 18 Months |
Quality Certification | CE, MSDS |
Safty Standard | ISO13485 |
Sample volume | 3 Full drops |
specificity | 99.00% |
sensitivity | 94.29% |
Storage Temperature | 2℃-30℃ |
Product Feature
Test Principle
This kit is an immunochromatography assay. According to the gold immunochromatographic test principle, double antibody sandwich method was used to detect SARS-CoV-2 nucleocapsid antigen in the samples. When there is virus antigen presence in the sample, the antigen binds with the corresponding colloidal gold monoclonal antibody and the coated monoclonal antibody at the detection line to form a compound and then condenses into a red band, indicating a positive result. If there is no antigen in the sample, complex cannot be formed at the detection line, and no red band is shown, indicating negative result.
Use Step
Result Interpretation
POSITIVE: Two (2) distinct colored lines appear. One line should be in the control region (C) and the other line should be in the test region (T).
NEGATIVE: One (1) colored line appears in the control region(C). No apparent colored line appears in the test region (T). The negative result does not indicate the absence of analytes in the sample, it only indicates the level of tested analytes in the sample is less than the minimum detection limit.
INVALID: No colored lines appear, or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.
Virus Sources
Global high frequency mutation | Alpha / B.1.1.7(U.K.) | Beta I B.1.351(South Africa) |
Gemma I P.1(Brazil) | Kappa I B.1.617.1(India) | Delta I B.1.617.2(India) |
C.37,ect | Alpha I B.1.17(U.K.) | B.1.36.16.etc |
A.2.5,etc | A.23.1 | Alpha I B.1.17(U.K.) |
B.1.1.33.etc | C.1.1.etc. |
Certificate
Contact Person: Ld
Tel: +8613480985156