Shanghai Eugene Biotech Co.,Ltd

Shanghai,China

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Shanghai Eugene Biotech Co.,Ltd

Shanghai,China

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Shanghai Eugene Biotech Co.,Ltd

Shanghai,China

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Antibodies to Human Immunodeficiency Virus type 1,2 and O combo test

FOB Price : Get a Price/Quote

Min.Order : 1 Set(s)

Certification : CFDA,GMP,ISO13485,CE,FDA

Brand Name : Eugene

Payment Terms : L/C,T/T,WesternUnion

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product information

brand name : Eugene
certification : CFDA,GMP,ISO13485,CE,FDA
min.order : 1 Set(s)
warranty :
payment terms : L/C,T/T,WesternUnion
Packaging :
Specification :
place of origin : China

product description

Model: Colloidal Gold Immunoassay Technologies Certification: ISO13485

Dimension:63cm*41cm*29cm Packaging Details: Eugene color pouch and inner box, fully packed in export cartons

Brand Name: Eugene Place of Origin: Shanghai

Warranty: 2 years Color: white

Size: strip/cassette/midstream Finish: 7-15Days

Customer's Logo: Eugene MOQ: 500pcs

Processing Time: 5-10 minutes

Usage: The EUGENE® HIV1.2.O Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of antibodies to HIV type 1, type 2 and Subtype O in human whole blood, serum or plasma. It is intended to be used as an aid for the diagnosis and management of patients related to infection with HIV and for screening of blood donors, or blood products as well. The test is recommended for professional use only. All results must be interpreted together with other clinical information or other diagnosis methods available to the physician.
Quality: sensitivity: 100% ; accuracy: 99.30%
Packaing: 25T/kit

SUMMARY
HIV (Human Immunodeficiency Virus) is the etiologic agent of Acquired Immune Deficiency Syndrome (AIDS). The virion is surrounded by a lipid envelope that is derived from the host cell membrane. Several viral glycoproteins are on the envelope. Each virus contains two copies of positive-sense genomic RNAs. HIV-1 has been isolated from patients with AIDS and AIDS-related complex, and from healthy people with high potential risk for developing AIDS.1 HIV-1 consists of Subtype M and Subtype O. Highly divergent strains of HIV-1 were first recognized in 1990 and grouped provisionally as Subtype O as this variation has similar glycoprotein markers to HIV-1 but a slight variation to the protein marker. Although rarely compared to HIV-1 and HIV-2. Infections caused by Subtype O have so far been identified in Africa (Cameroon), France and Germany. HIV-2 has been isolated from West African AIDS patients and from seropositive asymptomatic individuals.2 HIV-1, HIV-2, and Subtype O all elicit immune responses.3 Detection of HIV antibodies in serum, plasma or whole blood is the most efficient and common way to determine whether an individual has been exposed to HIV and to screen blood and blood products for HIV.4 Despite the differences in their biological characters, serological activities and genome sequences, HIV-1, HIV-2, and Subtype O show strong antigenic cross-reactivity.5,6 Most HIV-2 positive sera can be identified by using HIV-1 based serological tests.
The EUGENE® HIV1.2.O Rapid Test is lateral flow immunochromatographic assay for the qualitative detection of antibodies to HIV type 1, type 2, and/or Subtype O in human whole blood, serum or plasma specimen.
STORAGE&STABILITY
Store the kit in cool and dry places at a temperature between 2-30°C. Do not freeze. The shelf-life of the kit under these storage conditions is 24 months.

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