Colloidal Gold · Sexually Transmitted Disease
HIV 1/2 Antibody Rapid Detection Kit (Colloidal Gold)
Qualitative detection of HIV-1 and HIV-2 antibodies in human whole blood, serum, or plasma. The colloidal gold immunochromatographic assay aids in diagnosing HIV infection.
- SKU Code
- On request
- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of HIV-1 and HIV-2 antibodies in human whole blood, serum, or plasma. The colloidal gold immunochromatographic assay aids in diagnosing HIV infection.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Colloidal Gold |
| Application area | Sexually Transmitted Disease |
Epidemiology
The human immunodeficiency virus (HIV), responsible for acquired immunodeficiency syndrome (AIDS), is a retrovirus. Transmission can occur via infected blood or blood products, sexual contact, or from an HIV-positive mother to her child before, during, or after childbirth. Two distinct types, HIV-1 and HIV-2, have been identified.
Serological assays currently serve as the primary method for laboratory diagnosis of HIV. This test utilizes colloidal gold immunochromatographic technology to detect HIV infection, and its results are intended for reference purposes only.
| SKU code | On request |
|---|---|
| Target region | HIV-1/2 antibody |
| Storage temperature | 4℃-30℃ |
| Sample type | whole blood, serum and plasma |
| Shelf life | 12 months |
| Auxiliary instruments | Not required |
| Extra Consumables | Not required |
| Detection time | 15-20 mins |
| Specificity | No cross-reaction with Treponema pallidum, Epstein-Barr virus, hepatitis A virus, hepatitis B virus, hepatitis C virus, rheumatoid factor. |
| Approval | On request |
|---|---|
| Documents | Datasheet, IFU, SDS, COA / conformance, origin, and export documents where available |
FAQ
What should be confirmed before quotation?
Sample context, collection method, and extraction workflow should be confirmed before final kit selection.
Which documents can be requested?
Datasheet, IFU, SDS, COA / conformance, origin, insurance, and export documents can be checked where available.
Can the format be adjusted for different workflows?
Liquid or lyophilized format options should be confirmed together with instrument compatibility and shipment requirements.
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