Nasal Swab Self Test Rapid Antigen Test Kit At Home
Brand Name:Ascentet
Certification:CE FDA TGA
Model Number:Covid Test Kit
Minimum Order Quantity:10000pcs
Delivery Time:5-20 days
Payment Terms:T/T, Western Union, MoneyGram
Contact Now
Add to Cart
Active Member
Location:
Shanghai Shanghai China
Address:
703-1, Building 33, 258 Xinbrick Road, Hi-tech Park, Caohejing Development Zone, Shanghai
Supplier`s last login times:
within 1 hours
Product Details
Company Profile
Product Details
15mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit
Rapid Selftest Device Test
IgG will be appeared in the body's immune system during infection. IgG antibodies generally appear around 2-4 weeks, maintain a longer time, fade slowly, and the c
oncentration is relatively high. Detection of COVID-19 IgG antibody
has the advantages of high sensitivity, strong specificity, and
clear identification of previous virus infection. Therefore,
detection of novel coronavirus IgG antibody is of great
significance in epidemiological investigation.
IgG antibody appears later than IgM antibody, and it reaches the
peak in about four weeks. It can be in the body for a long time and
it is a sign of previous infection.
Rapid Selftest Device Principle
COVID-19(SARS-Cov-2)IgG Antibody Test Kit was determined by colloidal gold immunochromatography, for the detection of the antibody in human serum / plasma / whole blood specimens. After dropping, if the COVID-19-IgG antibody is existing in the specimen, it will form a Novel Coronvirus COVID-19 antigen and antibody complex along with the Novel Coronvirus antigen that marked in the gold pad. When the complex migrates to the detection line, it will combined with the anti- human IgG antibody that fixed there to form the Test line. The excess gold markers will combined with the polyclonal antibody that fixed at the control line to form the C line. So if the specimen contains COVID-19 antibody, two visible lines will be appeared. If there was no COVID-19 antibody in the specimen, only one visible line will be formed at the control line
HOW TO PERFORM THE TEST?
1. Remove a Test Device from the foil pouch by tearing at the notch and place it on a level surface.
2. Holding Extraction Reagent bottle vertically, add 10 drops (400μL) to the Extraction tube.
3. Insert the nasopharyngeal (and oropharyngeal) swab sample(s) into the extraction solution, then, mix the swab 10 times.
4. Remove the swabs while pressing against the solution tube in order to extract most of the specimen
5. Place the dropper cap and drop 3 drops (60~70μl) into the sample well.
6. Read the result in 10-15 minutes. Do not read results after more than 20 minutes.
Something you need to learn about:
1) What is the difference between an antigen test and a molecular
test?
An antigen test detects specific proteins on the surface of the
virus. These tests are quicker and less expensive, but have a
higher chance of missing an active infection, according to the FDA.
A molecular (PCR or polymerase chain reaction) test detects the
virus’s genetic material. These tests require a more complex
technology to get results, and it usually takes a day or two to get
those results (depending on lab capacity, results may take up to a
week).
If an antigen test shows a negative result and you have reason to
believe you may have the virus (because of symptoms or exposure),
your doctor may order a molecular test to confirm the results.
2) Which tests are more accurate?
No test is 100% accurate, but the molecular tests are considered to
be more accurate than the antigen tests, according to available
research.
According to the FDA, an antigen test cannot “definitively rule out
active coronavirus infection,” but positive results are “highly
accurate” (negative results may require a confirmation test).
Harvard Medical School wrote in August that the reported rate of
false negatives with molecular testing is as low as 2% and as high
as 37%. A molecular test using a deep nasal swab will have fewer
false negative results than samples from throat swabs or saliva,
they say.
For antigen testing, Harvard noted that the reported rate of false
negative results can be as high as 50%, but that the FDA has
granted emergency use authorization for a more accurate antigen
test.
In general, some of the issues that may affect the accuracy of a
test include ineffective swabbing, contamination or mishandling of
the sample, or problems with the testing chemicals, according to
the FDA.
3) If antigen tests are less accurate, why would we use them?
Experts say the value in the rapid antigen tests is in the
frequency of the testing rather than the accuracy, with repeated
testing recommended. According to Science, getting a false negative
in an antigen test two or three times in a row is rare. This
strategy lines up with the NPR report mentioned above, which would
employ daily testing of those in high-risk areas.
4) Who must be tested for COVID-19?
As per the Minister’s Directive: COVID-19: Long-Term Care Home
Surveillance Testing and Access to Homes (Minister’s Directive)
effective January 8, 2021, all staff, student placement and
volunteers working in long-term care homes must be tested regularly
in accordance with the Minister’s Directive, unless the exception
for individuals who have previously had laboratory confirmed
COVID-19 applies. The testing requirements in the Minister’s
Directive include all individuals working in long-term care homes
who are: • Staff as defined in the Long-Term Care Homes Act, 2007 •
Volunteers as defined in the Long-Term Care Homes Act, 2007 •
Student placement, meaning any person working in the long-term care
home as part of a clinical placement requirement of an educational
program of a college or university, and who does not meet the
definition of “staff” or “volunteer” under the Long-Term Care Homes
Act, 2007. The Minister’s Directive also includes additional
testing and documentation requirements for general visitors,
caregivers and support workers.
Nasal Swab Self Test Rapid Antigen Test Kit At Home
Inquiry Cart
0