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Hiv 1+2 Rapid Test

Supplier From Romania
Nov-24-10

See now human immunodeficiency virus type 1 and 2 (hiv-1/2) antibody test is a rapid and convenient immunochromatographic in vitro assay. It is used for detection of antibodies to hiv-1/2 in human serum, plasma or whole blood.

30 cassettes in a plastic box.

Price and Minimum Quantity

Price: $0.6
MOQ: Not Specified

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One-Step HIV Ab Rapid Test is to detect the antibodies in serum, plasma or whole blood.
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Product Description
One-Step HIV1/2 Rapid Test
One-Step HIV1/2 Rapid Test is to detect the antibodies against HIV 1/2 in serum, plasma or whole blood.General InformationNo instruments neededApplied highly purified HIV recombinant proteins : p24 ,gp41 and gp36Detect HIV type1 and type2 with separate test lines at one timeSensitivity : 99.9% , Specificity : 99.5%Specimen : Serum , Plasma or Whole Blood , or UrineReading Time : 10 min
Product Feature
format:strip/cassette/uncut sheet
MOQ:1000pcs
sensitivity:99.9%
specificity:99.5%
specimen:WB/S/P
Product Specification/Models
package:neutral pouch bulk package/OEM package
Application
One-Step HIV1/2 Rapid Test is to detect the antibodies against HIV 1/2 in serum, plasma or whole blood.
Payment
T/T and western union
Delivery
7-15 work days
Origin
China
Minimum Order
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Uncut Sheet Hiv 1/2 Tri-Lines Rapid Test

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Package:30sheets/pouch

Specimen:Whole blood/Serum/plasma

INTENDED USE

The HIV-1/2 Rapid Screen Test (RST) is a qualitative test for the detection of antibodies to Human Immunodeficiency Virus type 1 and 2(HIV-1/2) in human serum/plasma and whole blood. It is considered as an initial screening test for HIV-1/2 antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA.

PRECAUTION

1.For in vitro diagnostic uses only.

2.All patient samples should be treated as if capable of transmitting diseases.

3.Do not use test kit beyond expiration date.

4.Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.

SUMMARY AND EXPLANATION OF THE TEST

It has been shown that the acquired immunodeficiency syndrome (AIDS) is caused by viruses transmitted by sexual contact, transfusion, use of contaminated blood products and sharing contaminated needles. HIV-1 and HIV-2 viruses have been isolated from patients with AIDS and AIDS-related complex (ARC), high-risk persons for AIDS. HIV-1 and HIV-2 viruses delete T helper cells, a subpopulation of T cells for body defense, thus causing AIDS patients susceptible to opportunistic infections and developing malignant tumors. The incidence of specific antibodies to HIV-1/2 is high in AIDS, ARC and persons with high risk for AIDS. The HIV-1/2 Rapid Screen Test is designed to detect antibodies to HIV-1/2 in AIDS patients, ARC or high risk persons and identify any potential donors carrying these antibodies in serum specimens.

PRINCIPLE

HIV-1/2 RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HIV-1/2 in human serum/plasma and whole blood. HIV-1/2 specific antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HIV-1/2 specific antigens. Antibodies to HIV-1/2, if present, a red colored band will develop on the membrane in proportion to the amount of HIV-1/2 antibodies present in the specimen. Absence of this red colored band in the test region suggests a negative result. To serve as a procedural control, red colored band in the control region will always appear regardless the presence of antibodies to HIV-1/2.
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Pre-Clinical Test Report
Accuracy
- In total samples 93.3% (14/15) - In positive samples 91.7% (11/12)

1. Pre-Clinical Test summary

1) Pre-clinical test is fulfilled by Domestic large clinical laboratory with ADTech COVID-19 IgM/IgG RAPID KIT
2) Tests are made by total 15 samples with 12 positive and 3 negative samples
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2. Pre-clinical test result

1) Samples were tested by ADTech COVID-19 IgM/IgG RAPID KIT
2) Test result by ADTechs RAPID KIT
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3) Comparison between Immunofluorescence analysis and ADTechs RAPID KIT
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GCMS manufactures COVID-19 antigen test kit, the GENEDIA W COVID-19 Ag which is listed on the EU common list, also with GMP and ISO certifications. GENEDIA W COVID-19 Ag is unaffected based on the in-silicon analysis of the mutations in the nucleocapsid (N gene) of Omicron viruses. Letter of statement is available upon your request.

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Price and Minumum Quantity
Price FOB in USD: negotiable 0.8 to 1.8Minimum Order Qty: None Pieces
Production Capacity: 3,000,000/monthPackaging: 20 Tests/kit, 30 Kits/box, 12 Boxes/pallet
Sample: Available. Sample Cost Born By Supplier
Product Model And Origin
Brand: GENEDIAModel: 643G-S (Saliva)
Seller Code: Genedia w covid 19 agHS Code: 3002.15
Standards: Ce
Competitive Advantages
Allow wider testing with fast test time (10 minutes)
All necessary materials provided / no equipment needed
Sensitivity: 93.33%, specificity: 100%
Free sample. no moq. price is negotiable. customized packing.
Other Details
20 tests / kit
24 months from the date of manufacture
2 ~ 30c(35.6 ~ 86f) available for room temperature deliver
In stock. fast delivery.
1 x Instructions for Use Manual
40 x Test Cassettes
1 x Buffer
40 x Dropper

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