Product Details:
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Sensitivity: | 95% | Specificity: | 99.1% |
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Test Time: | 15 Minutes | Storage Condition: | 2-30℃ |
Product Feature: | Quick To Know Test Result With High Sensitivity&specificity | ||
High Light: | FDA in vitro diagnosis antigen swab test,FDA 95% sensitivity antigen swab test,FDA 95% sensitivity igm igg rapid test |
Product description:High Quality Home Antigen Rapid Test Kit
Antigen Rapid Test Kit is faster and less intrusive than a Polymerase Chain Reaction(PCR)test.This makess it easy for the public to use to test themselves if needed.In general,Antigen Rapid Test Kid has a sensitivity(ability of a test to identify patients with the disease)of about 95% for cases with higher viral loads and a specificity(ability of a test to identify patients without the disease)range of 99.1%.As the sensitivity and specificity of Antigen Rapid Test Kit are lower as compared to PCR tests,if you test Antigen Rapid test Kit positive or invalid twice,you will need to follow up with a confirmatory PCR test.You should not repeat the Antigen Rapid Test Kit.Even if you do test negative in the repeated test,it may be a false negative result and hence you need to go for a confirmatory PCR test.Poweray Antigen Rapid Test Kits has good performance and with high sensitivity to detect the antigen at the early stage of infection.High performance rapid test enable immediate treatment or isolation measures to minimize transmission
Principle of Detection:
The kit is an immunoassay kit based on the principle of dual antibody sandwich technology. The ncov monoclonal antibody of 2019 labeled as labeled on the binding pad. In the test procedure, Combined to the ag 19 cov monoclonal antibody of 2019 ncov ag in the labeled test material, The ag―ab complex was captured by another 2019 ncov monoclonal antibody, Moving upward through the capillary effect, Until the sandwich complex is formed. If the NCO VAG of 2019 exists in the sample, The red band appears in the T area of the explanation window. Otherwise, The result is negative. The Control Line (C) is used for program control. If the test program runs successfully, It must always be displayed.
Product usage:
This kit is used for vitro qualitative detection of coronavirus(Covid-19) in human pharyngeal or nasal secretions,sailva samples.
Used as a supplementary test indicator for suspected cases of new coronavirus nucleic acid test negative or used in conjunction with nucleic acid testing in the diagnosis of suspected cases
Product advantage:
Storage Conditions and Validity:
Keep it at 2℃~30℃, and the validity period is tentatively set at 24 months.
Aluminum foil bag is svalid for 4 hour
Production lot number:see details label
For more information:see label
Test procedure:
Detailed explanation of test results:
Symboals on labels:
Contact Person: Ms. Carina
Fax: 86-755-89366646