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MDA Igm Igg Rapid Antigen Novel Saliva Test Kit

Name: MDA Igm Igg Rapid Antigen Novel Saliva Test Kit
Brand: Ascentet
Price: 1.50 USD

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Brand Name :	Ascentet
Model Number :	Covid Test Kit
Certification :	CE FDA TGA
Price :	$1.50-2.0/pcs
Payment Terms :	T/T, Western Union, MoneyGram
Supply Ability :	100000pcs/day
Delivery Time :	5-20 days

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MDA Igm Igg Rapid Antigen Novel Saliva Test Kit

15mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit

Product Description

REAGEN This kit is a full-component lyophilized fluorescent PCR reagent for patients with suspected cases of pneumonia, suspected aggregation cases of COVID-19 infection, and other patients who need to undergo clinical diagnosis of new coronavirus infection. The COVID-19 ORF1ab and N genes were specifically tested.

Detection Principle

REAGEN The COVID-19 nucleic acid detection kit is based on reverse transcription PCR combined with fluorescent probe amplification detection technology. Fluorescent labeling of specific fluorescent probes. 5'is labeled with a fluorescent reporter group and 3'is labeled with a fluorescent quencher group. Before amplification, the fluorescent signal of the reporter group is absorbed by the quencher group and cannot excite the fluorescent signal; during the PCR amplification process, Taq polymerase The 5'-3' exonuclease activity cuts off the fluorescent group of the probe, separates the fluorescent reporter group and the fluorescent quencher group, enables the fluorescence monitoring system to receive the fluorescence signal, and records the increase of the fluorescence level by the fluorescence PCR instrument .

Kit Contents, Storage and Shelf Life

REAGEN Table1:COVID-19 Real-Time Fluorescence PCR Detection Kit (lyophilized)

Component	Amount
RT-PCR Mix	1 bottle
Positive control (lyophilized powder)	1 tube
Negative control	1 tube
Manual	1

INTEND USE

The rapid test kit is used for qualitative determination of novel coronavirus (SARS-CcV-2) antigen in human nasal swab samples in vitro.. This kit is offered to clinical laboratories and healthcare workers for point-of-care testing, and not for at home testing, in compliance with Section IV.D. of the FDA’s Policy for COVID-19 Diagnostic Test.

MAIN COMPONENTS
• Test Cassette.
• Extraction Tube.
• Extraction Reagent.
• Nasal/Oral Swab.
• Working Holder.

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.

Rapid Test Kit Antigen Self Test in 15 mins Nasal Swab 0

Rapid Test Kit Antigen Self Test in 15 mins Nasal Swab 1

Rapid Test Kit Antigen Self Test in 15 mins Nasal Swab 2

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MDA Igm Igg Rapid Antigen Novel Saliva Test Kit

MDA Igm Igg Rapid Antigen Novel Saliva Test Kit

MDA Igm Igg Rapid Antigen Novel Saliva Test Kit

15mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit

Product Description

Detection Principle

Kit Contents, Storage and Shelf Life

15 Mins Antigen Novel Saliva Test Kit

MDA Igm Igg Rapid Antigen Novel Saliva Test Kit

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