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Lepu Medical SARS-CoV-2 Antigen rapid test (front nasal swab) – box of 25
Lepu Medical SARS-CoV-2 Antigen rapid test (front nasal swab) – box of 25
very easy test execution by test card
- very simple sample implementation without tubes
- Smear from the front of the nose
- Test result in 15 minutes
- Verifiably recognizes the Delta variant
- BfArM listed and evaluated by the Paul Ehrlich Institute (PEI)
- Sensitivity 92.00%
- Specificity 99.26%
- Omikron / Delta / Epsilon virus detection
1 box contains 25 tests with 25 test liquids
Sie sind interessiert an Großmengen oder Rahmenverträgen zu besonders attraktiven Preisen?
0,99 € – 1,29 € zzgl. Mwst. Stück
immediately available |
Lieferzeit: about 1-2 business days
Einheit | Mengen | Stückpreis |
---|---|---|
box | 25 – 425 | 1,29 € |
carton | 450 – 4.500 | 1,14 € |
Pallet small | 4.950 – 10.350 | 1,09 € |
Large range | 10.800 – 43.200 | 0,99 € |
Einheit wählen für Staffelpreis
3% Rabatt für Vorbesteller Jetzt für Lieferung in KW28 vorbestellen und 3% Rabatt auf alle Mengen erhalten.
GUTSCHEIN CODE: LIEFERUNG-KW28
GUTSCHEIN CODE: LIEFERUNG-KW28
Produktdetails
further information
scope of delivery
application
Delivery Restriction
Zertifikate/Dokumente
Produkt anfragen
What is the LEPU Medical SARS-CoV-2 Rapid Antigen Test?
The novel coronavirus (SARS-Cov-2) rapid antigen test is an in vitro diagnostic test for the qualitative detection of novel coronavirus antigens in nasopharyngeal swabs and oropharyngeal swabs using the rapid immunochromatographic method. The identification is based on the monoclonal antibodies specific for the new coronvirus antigen. This product is intended for professional use in the laboratory and at the point of care.
The current test card is based on specific antibody-antigen reaction and immunoassay technology.
The test card contains a colloidal gold-labelled SARS-CoV-2 N protein monoclonal antibody pre-coated on the combination pad, a matching SARS-CoV-2 N protein monoclonal antibody immobilized on the test area (T). , and a corresponding antibody in the quality control area (C). During testing, the N-protein in the sample binds to the colloidal gold-labeled N-protein monoclonal antibody SARS-CoV-2 pre-coated on the combination pad. The conjugates migrate upwards by capillary action and are then captured by the N-protein monoclonal antibody immobilized in the test area (T). The higher the level of N-protein in the sample, the more conjugates are captured by the conjugates and the darker the color in the test area. If there is no virus in the sample or if the virus content is lower than the detection limit, no color can be seen in the test area (T). A purple stripe will appear in the Quality Control area (C) regardless of whether the virus is present in the sample or not. The purple stripe in the quality control area (C) is a criterion for judging whether there is enough sample or not and whether the chromatographic process is normal or not.
The kit is ready to use and contains all the components needed to perform a test.
Scope of delivery of a box:
- 25x SARS-CoV-2 test card
- 25x Sample Extraction Buffer (0.3mL)
- 25x disposable swabs for sample collection
- 1x instruction manual
Additional Materials Required
- timer / clock
Positive (+): Purple streaks appear
both in the quality control area (C) and in the test area (T).
Negative (-): There is only one purple streak in the quality control area (C) and no purple streaks in either test area (T).
Invalid: There is no purple stripe in the Quality Control area (C), or there is a blue stripe in the Quality Control area (C), indicating incorrect operating procedures, or the test card is already unusable. In this case, read the instructions for use again carefully and then use a new test card. If the problem persists, stop using the products with the same lot number and contact the local suppliers immediately.
We would like to point out that in-vitro tests are intended for professional use and are only available to medical professionals! By ordering, you confirm that you belong to the group of medical professionals or that these tests will only be used and evaluated by medical professionals (e.g. general practitioner or company doctor).