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.
Specification Strength/ Size Packing Size Packed In HIV 1 & 2 Card Test Triline 50 Tests 50 Box Pack
General Information One-Step HIV Ab Rapid Test is to detect the antibodies in serum, plasma or whole blood. Applied highly purified HIV recombinant proteins: gp120 ,gp41 and gp36 antibody, detect HIV type1,type2 with combining or separate test lines at one time. Sensitivity : 100% , Specificity : 100% Specimen : Serum , Plasma ,Whole Blood , or Urine Reading Time : 10 min
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 1000pcs
Uncut Sheet HIV 1/2 Tri-Lines Rapid Test 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.
The test shows the presence in blood or serum of HIV antibodies (both type 1 and type 2).
Hiv test kit 99% above sensitivity and specificity Anti-hiv 1/2 or anti-hiv tri-line, which can tell hiv 1 or hiv 2 positive seperately Single pouched, then in bulk or in box
SARS-CoV-2 Rapid Antigen Test kit Colloidal Gold Method Medical Simple Rapid Convenient Sensitivity : 98.4% Specificity : 98.1% Test Time : 10-15min
Covid-19 Self Test Kit We are the authorized first vendor of ADTech! KFDA CE approved, FDA Pending Price : Negotiable 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 3) Clinical Laboratory tested the sample with Immunofluorescence Analysis 2. Pre-clinical test result 1) Samples were tested by ADTech COVID-19 IgM/IgG RAPID KIT 2) Test result by ADTechs RAPID KIT - 4 negatives and 11 positives results in 15 samples 3) Comparison between Immunofluorescence analysis and ADTechs RAPID KIT - 14 test results are same(including negative and positive results) - 1 samples test result are different(Positive Negative by ADTech
For in vitro qualitative detect of Covid-19 antigen in nasal(NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days of the onset of the symptoms. This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, and not for at home testing. 1.Easy to collect samples simple operation without professional equipment. 2.The test results are available in 15 minutes, and the test results are clearly visible. 3.Convenient transportation and low price, higher accuracy. 4.Suitable for large-scale rapid screening. Shelf life: 24 Months Test Result time: 10 Mins Packing: 25 Pieces per Box
