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Hangzhou AllTest Biotech CO.,LTD 

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High quality and sensitivity Rapid Test Reader HIV 1.2.O with CE

Product Details:

Place of Origin:China
Brand Name:AllTest
Certification:CE, ISO13485
Model Number:IHI-R402

Payment & Shipping Terms:

Minimum Order Quantity:N/A
Price:Negotiation
Packaging Details:20cassette/box
Delivery Time:2-4 Weeks
Payment Terms:Ex works
Supply Ability:10 M tests/month
Detailed Product Description
Format: Strip, Cassette, Uncut Sheet Accuracy: 99.2%
Specimen: Whole Blood/Serum/Plasma Time Of Use: One Time Use Only
Sample: Available Shelf Time: 24 Months

 

High quality and sensitivity Rapid Test Reader HIV 1.2.O with CE

 

Application:

 

The HIV 1.2.O Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies to Human Immunodeficiency Virus (HIV) type 1, type 2 and subtype O in whole blood, serum or plasma to aid in the diagnosis of HIV infection.

 

Description:

 

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 HIV 1.2.O Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid test to qualitatively detect the presence of antibodies to HIV type 1, type 2, and/or Subtype O in whole blood, serum or plasma specimen.
 
How to use?
 
Allow the test, specimen, buffer and/or controls to reach room temperature (15-30°C) prior to testing.
1.Exact QR Code from the QR code card for specific information of the test. Use only QR code card provided inside the test kits
2.Bring the pouch to room temperature before opening it. Remove the test cassette from the sealed pouch and use it as soon as possible.
3.Place the cassette on a clean and level surface.
For Serum or Plasma specimen: Hold the dropper vertically and transfer 1 drop of serum or plasma (approximately 25μL) to the specimen area, then add 1 drop of buffer (approximately 40μL),and start the timer, see illustration below.
For Venipuncture Whole Blood specimen: Hold the dropper vertically and transfer 2 drops of whole blood (approximately 50μL) to the specimen area, then add 2 drops of buffer (approximately 80μL), and start the timer. See illustration below.
For Fingerstick Whole Blood specimen:
·To use a capillary tube: Fill the capillary tube and transfer approximately 50μL of fingerstick whole blood specimen to the specimen area of test cassette, then add 2 drops of buffer (approximately 80μL) and start the timer. See illustration below.
4.Wait for the colored line(s) to appear. The result should be read with the AllTestTM LF Reader at 10 minutes.
5.For AllTestTM LF Reader installation, start up and complete instructions refer to the AllTestTM LF Reader User Manual. Operator must consult the AllTestTM LF Reader User Manual prior to use and become familiar with the processes and quality control procedures.
Note: It is suggested not to use the buffer, beyond 6 months after opening the vial.
High quality and sensitivity Rapid Test Reader HIV 1.2.O with CE
 
 
 
 
 

 

 
 

 

INTERPRETATION OF RESULTS


Results read by Alltest LF reader


The result of positive or negative for HIV 1.2.O infection is determined by the Alltest LF reader.


Result could be exported to excel.

 

Contact Details
Hangzhou AllTest Biotech CO.,LTD

Tel:86-571-56267891

Fax:86-571-56267856

Contact Person: Mrs. Selina

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