Home Use COVID-19 Rapid 19 Rapid Ag Test Kit,Rapid Test Kit Antigen
OEM Service
The COVID-19 Antigen Rapid Test device is a lateral flow
chromatographic immunoassay for the qualitative detection of the
nucleocapsid(N) protein antigen from SARS-CoV-2 in nasopharyngeal
swab, oropharyngeal swab. It provides an aid in the diagnosis of
infection with 2019-nCOV.
| Product Name | Home Use COVID-19 Rapid 19 Rapid Ag Test Kit,Rapid Test Kit Antigen
OEM Service |
| Formats | Device(4mm) |
| Place of Origen | China |
| Specimen | Swab |
| Read Time | 15 minutes |
| Shelf life | 2 years |
| Package | 25 device/box or 1Test/Box |
| Storage | 2℃-30℃ |
[SUMMARY]
The novel coronaviruses belong to the β genus. COVID-19 is an acute
respiratory infectious disease. People are generally susceptible.
Currently, the patients infected by the novel coronavirus are the
main source of infection; asymptomatic infected people can also be
an infectious source. Based on the current epidemiological
investigation, the incubation period is 1 to 14 days, mostly 3 to 7
days. The main manifestations include fever, fatigue and dry cough.
Nasal congestion, runny nose, sore throat, myalgia and diarrhea are
found in a few cases.
[PRINCIPLE]
The Device uses the principle of the double antibody sandwich
method for detecting the nucleoprotein (N) of SARS-CoV-2. The
marker is composed of the anti-N antibody 1 labeled with colored
particles. When testing, the sample was added into the sample well
and migrated to the
absorbent pad by the capillary effect. If the virus exists, it will
react with the marker and captured by the anti-N antibody 2 coated
in the NC membrane. Then there is a colored line produced at the
test area, indicating a positive result. If there is no virus in
the sample, the colored line will not show at the test area and it
means a negative result. Regardless of whether the virus contained
in the sample, as a procedural control, a colored line will always
appear at the control area, indicating that proper volume of
specimen has been added and the correct test procedure is
conducted.
