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Aids Rapid Test 4th Gen HIV Ab AG Rapid Test Kit

China Aids Rapid Test 4th Gen HIV Ab AG Rapid Test Kit, Find details about China HIV Ab AG Test Kit, HIV Test Kit from Aids Rapid Test 4th Gen HIV Ab AG Rapid Test Kit

Model NO.
HIV0123
Trademark
Neo nostics
Origin
Jiang Su, China
Model NO.
HIV0123
Trademark
Neo nostics
Origin
Jiang Su, China
Aids Rapid Test 4th Gen HIV Ab AG Rapid Test Kit
The HIV 4th gen test kit is a lateral flow immunoassay for the simultaneous detection and differentiation of anti-HIV-1/ anti-HIV-2 antibodies (IgG, IgM,IgA) and P24 antigen in human serum, plasma, or whole blood. It is intended to be  used as a screening test and as an aid in the diagnosis of infection with HIV. Any reactive specimen with the HIV 4th gen test kit must be confirmed with alternative testing method(s) such as ELISA or PCR.
Aids Rapid Test 4th Gen HIV Ab AG Rapid Test Kit
 
Product Name
HIV Ab /Ag Plus Combo Rapid Test
Brand Name
Neo nostics , OEM-Buyer's logo
Specimen
Fingerstick Whole Blood/Venous Whole Blood/Serum
Format
Cassette
Relative 
97.7%
Reading time
1-20mins
Shelf time
24 months
Storage
2ºC to 30ºC

TEST PROCEDURE

Step 1: Bring the specimen and test components to room temperature if refrigerated or frozen. Mix the specimen well prior to assay once thawed. 
Step 2: When ready to test, open the pouch at the notch and remove device. Place the test device on a clean, flat surface. 
Step 3: Be sure to label the device with specimen's ID number. Step 4: For whole blood test Apply 2 drops of whole blood (about 50-60 μL) into the sample well. Then add 1 drop (about 35-50 µL) of Sample Diluent immediately.

For serum or plasma test
Fill the pipette dropper with the specimen. Holding the dropper vertically, dispense 2 drops (about 50-60 μl) of specimen into the sample well making sure that there are no air bubbles Then add 1 drop (about 35-50 µL) of Sample Diluent immediately

Step 5: Set up timer.
Step 6: Results can be read in 15 minutes. Positive or reactive results can be visible in as short as 1 minute. Don't read result after 15 minutes. To avoid confusion, discard the test device after interpreting the result.
 
INTERPRETATION OF RESULTS

Negative: If only the C band is present, the absence of any burgundy color in the both test bands (Ag and Ab) indicates that no HIV antibodies or P24 antigen are detected in the specimen. The result is negative or non- reactive

HIV -1+2 Antibody Positive: In addition to the presence of C band, if Ab band is developed, the test indicates presence of antibodies to HIV-1+2 in the specimen. The result is HIV-1+2 positive or reactive

HIV -1+2 Antien Positive: In addition to the presence of C band, if Ag band is developed, the test indicates presence of antigen to anti-P24 antibody in the specimen. The result is HIV-1/2 positive or reactive.

HIV -1+2 Antibody & Antigen Positive: In addition to the presence of C band, if both Ab and Ag bands are developed, the result is also HIV positive or reactive. For differentiation of the type of HIV virus infection, dilute the test specimen with Sample Diluent at 1:50 or 1:100 dilution, then retest the diluted specimen with a new test device .
Samples with positive or reactive results should be confirmed with alternative testing method(s)such as ELISa or PCR and clinical findings before a diagnostic decision is made.

Invalid: If no C band is developed, the assay is invalid regardless of any burgundy color in the T bands as indicated below. Repeat the assay with a new device.

PACKAGING DETAILS

1. Each box contains 30 test devices, each sealed in a foil pouch with three items inside:  one cassette device , one desiccant and one 5 µL mini plastic droppers.
2. buffer (1 bottle, 6 mL)
3. One package insert (instruction for use).


1 test/pouch, 50 or 100 tests/box for strip;
1 test/pouch, 25 or 30 tests/box for cassette.

COMPANY PROFILE
Aids Rapid Test 4th Gen HIV Ab AG Rapid Test KitAids Rapid Test 4th Gen HIV Ab AG Rapid Test Kit

PRODUCTION PROCESS
Aids Rapid Test 4th Gen HIV Ab AG Rapid Test Kit
FAQ

Q1.What's the method you use to do the test?

A: Colloidal Gold Method.

Q2: What's ur MOQ ?
A: Always, for strip format, the MOQ is 5000pcs. While for cassette format, MOQ is 2000pcs, same as midstream.  

Q3: What's your packing of the tests?
A: If you choose the low cost, we will suggest you the bulk packing to go. Which means 1 test in a single pouch, then 100/25 pouches in a plastic bag, 50 bags in a carton. If you need to sell in pharmacy/chain shop or some countries which have strict requirements about the packing, you can choose to pack in a box, like 30 pcs in a box, or even 1 test in a single box.

Q4: What's the main differences when comparing products from different suppliers?
A: You can compare the mainly features of the test: Accuracy, Sensitivity, Specificity, and then the Price.

Q5: Some tests can be tested with serum/plasma or with whole blood, so what's the difference?
A: Well, if the specimen is whole blood, people will need buffer, lancet and alcohol swab to help the test. If they buy all the accessories, they can test very easily at home. But if the specimen is serum/plasma, it will need centrifuge to separate serum from whole blood first. This way, it's better to use at lab or hospital. And in some words, serum/plasma test will always give a more accurate results.

Q6: How can i distinguish a good test kit?
A: You can judge from the 4 facts: 
1. Technical data: Such as the accuracy, specificity and sensitivity.
2. Pouch sealing: Tight enough. If the foil pouch is not sealed well, the humidity in circustance will destroy the reactivity of antibodies labeled on NC membrane. Shelf life will be shorten down.
3. Flow speed: The shorter the better??  NO!!   The reaction of antibodies on NC membrane and antigens in specimen usually requires quite a while to work sufficiently. You can refer to the instruction for more accurate time.
4. Background: Good test usually gives clean background after running. If there are red smears in the reading window, it usually caused by bad colloidal gold technology or bad NC membrane. Sometimes, the defect caused false positive result in practice.

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