40 Test Kit + 10 Free in this kit
A rapid test for the diagnosis of Human Immunodeficiency Virus to detect antibodies to HIV type 1, type 2 and Subtype O qualitatively in Serum or plasma. For professional in vitro diagnostic use only. The HIV 1/2/O Rapid Test Cassette 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 serum or plasma to aid in the diagnosis of HIV infection. HIV (Human Immunodeficiency Virus) is the etiologic agent of Acquired Immune Deficiency Syndrome (AIDS). Aspen Hiv Rapid 40 Test Kit
Aspen Hiv Rapid 40 Test Kit Serum or Plasma
Naco Guideline on HIV Testing
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 1 complex, and from healthy people with high potential risk for developing AIDS. 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 2 3 individuals. HIV-1, HIV-2, and Subtype O all elicit immune responses. Detection of HIV antibodies in serum, plasma is the most efficient and common way to determine 4 whether an individual has been exposed to HIV and to screen blood and blood products for HIV.
Despite the differences in their biological characters, serological activities and genome sequences, 5,6 HIV-1, HIV-2, and Subtype O show strong antigenic cross-reactivity. Most HIV-2 positive sera can be identified by using HIV-1 based serological tests. The HIV 1/2/O Rapid Test Cassette Serum Plasma is a rapid test to qualitatively detect the presence of antibodies to HIV type 1, type 2, and/or Subtype O in serum or plasma specimen.
The HIV 1/2/O Aspen Hiv Rapid 40 Test Kit Rapid Test Cassette Serum/Plasma is a qualitative, membrane based immunoassay for the detection of antibodies to HIV-1, HIV-2, and Subtype O in serum or plasma. The membrane is pre-coated with recombinant HIV antigens in the test line regions, T1 and T2. The T1 test line is pre-coated with HIV-1 and Subtype O antigen and the T2 test line is precoated with HIV-2 antigen.
During testing, the serum or plasma specimen reacts with HIV antigen coated particles in the test strip. The mixture then migrates upward on the membrane chromatographically by capillary action and reacts with recombinant HIV antigen on the membrane in the test line region. If the specimen contains antibodies to HIV-1 and/or Subtype O, or HIV-2, one colored line will appear in the test line region; if the specimen contains antibodies to HIV-1 and/or Subtype O, and HIV-2, two colored lines will appear in the test line region.
Both indicate a positive result. If the specimen does not contain HIV-1, Subtype O, and/or HIV-2 antibodies, no colored line will appear in the test line region indicating a negative result. To serve as a procedural control, a colored line will always appear in the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. The test contains HIV type 1, type 2, and Subtype O recombinant antigens coated particles and HIV type 1, type 2, and Subtype O recombinant antigens coated on the membrane.
• For professional in vitro diagnostic use only. Do not use after expiration date. • Do not eat, drink or smoke in the area where the specimens or test cassettes are handled. • Do not use test if pouch is damaged. • Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout all procedures and follow the standard procedures for proper disposal of specimens.
• Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are assayed. • Aspen Hiv Rapid 40 Test Kit The used test should be discarded according to local regulations. • Humidity and temperature can adversely affect results. Store as packaged in the sealed pouch either at room temperature or refrigerated (2-30°C). The test is stable through the expiration date printed on the sealed pouch.
The test must remain in the sealed pouch until use. DO NOTFREEZE. Do not use after the expiration date. The Aspen Hiv Rapid 40 Test Kit HIV 1/2/O Rapid Test Cassette Serum Plasma can be performed using serum or plasma. Testing should be performed immediately after the specimens have been collected. Do not leave the specimens at room temperature for prolonged periods.
Serum and plasma specimens may be stored at 2-8°C for up to 3 days. For long term storage, specimens should be kept below -20°C. Whole blood collected by venipuncture should be stored at 2-8°C if the test is to be run within 2 days of collection. Do not freeze whole blood specimens.
in Aspen Hiv Rapid 40 Test Kit Whole blood collected by fingerstick should not be tested. • Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly.
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POSITIVE:* Two or three distinct colored lines appear. One line should always appear in the control line region (C), and another one or two apparent colored line(s) should appear in the test line region(s) (T1 and/or T2). *NOTE: The intensity of the color in the test line region (T1 and T2) will vary depending on the concentration of HIV antibodies present in the specimen. Therefore, any shade of color in the test line region (T1 and/or T2) should be considered positive.
NEGATIVE: One colored line appears in the control region (C). No apparent colored lines appear in the test line regions (T1 and T2). INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor
Aspen HIV 1/2/O Rapid Test is a professional HIV antibody screening assay designed for qualitative detection of antibodies associated with HIV-1, HIV-2 and the stated HIV-1 subtype coverage in the specimen types specified by the manufacturer.
Because this is an antibody screening test, it should not be interpreted as an HIV p24 antigen test or as a fourth-generation HIV antigen/antibody assay.
A Reactive result on a single HIV screening assay should proceed through the applicable HIV diagnostic testing algorithm.
HIV diagnosis should not be based on one Reactive screening device alone.
HIV Screening vs Confirmatory Testing: Why One Reactive Rapid Test Is Not a Final Diagnosis
HIV Rapid Test Kit Complete Guide
Understand HIV antibody testing, Reactive and Non-Reactive result interpretation, testing-window considerations and how rapid assays fit into a wider HIV testing pathway.
An antibody test may not detect infection during the early period after acquisition before sufficient antibodies have developed.
Therefore, a Non-Reactive result should not automatically be used to exclude very recent HIV infection when clinical or exposure history suggests that further evaluation is appropriate.
HIV Testing During Pregnancy & Antenatal Care
HIV screening is an important component of antenatal care. Appropriate diagnostic testing and timely linkage to care support maternal health and prevention of vertical transmission.
Rapid Diagnostic Tests for Gynecology & Antenatal Clinics: Pregnancy, HIV, HBsAg, HCV & Syphilis
This professional guide explains how HIV testing relates to pregnancy, HBsAg, syphilis and HCV screening while keeping each infection-specific diagnostic pathway separate.
Rapid Test Do’s & Don’ts: HIV, HBsAg, HCV & Syphilis Sample Handling, Storage & Common Errors
Review specimen handling, pouch integrity, expiry, storage, timing, procedural controls, documentation and other practices that can affect rapid-test reliability.
Professional-use note: Always follow the exact current Aspen Instructions for Use for specimen type, collection and storage, sample volume, timing, controls and interpretation. Test-line darkness should not be used to estimate HIV viral load, disease stage or clinical severity.
Aspen Hiv Rapid 40 Test Kit
Legal Disclaimer: this is an diagnostic product to be used in or by medical professional expert supervision only Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and cross verify with ELISA / PCR Methods at your diagnostic centre or referral diagnostic laboratory
