Fluorescence PCR · Others
HIV-1 Quantitative Detection Kit (Fluorescence PCR)
Quantitative detection of human immunodeficiency virus type 1 (HIV-1) RNA in serum or plasma samples. Useful for monitoring HIV-1 viral load in clinical settings.
- SKU Code
- On request
- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Quantitative detection of human immunodeficiency virus type 1 (HIV-1) RNA in serum or plasma samples. Useful for monitoring HIV-1 viral load in clinical settings.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Others |
Epidemiology
HIV-1 (Human Immunodeficiency Virus type 1) resides in the bloodstream and progressively dismantles the body's immune defenses. This loss of immunity makes individuals vulnerable to untreatable infections and cancers, ultimately causing death. The virus spreads via sexual contact, blood exposure, and vertical transmission from mother to child.
Reagent required but not provided
Nucleic acid extraction reagents.
| SKU code | On request |
|---|---|
| Storage | -18℃ |
| Shelf-life | 12 months |
| Specimen Type | Serum or Plasma samples |
| CV | ≤5.0% |
| LoD | 40IU/mL |
| Applicable Instruments | Applicable to type I detection reagent: Applied Biosystems 7500 Real-Time PCR Systems, QuantStudio ® 5 Real-Time PCR Systems, SLAN-96P Real-Time PCR Systems (Hongshi Medical Technology Co. Ltd.), LineGene 9600 Plus Real-Time PCR Detection Systems (FQD-96A, Hangzhou Bioer technology), MA-6000 Real-Time Quantitative Thermal Cycler (Suzhou Molarray Co. Ltd.), BioRad CFX96 Real-Time PCR System, BioRad CFX Opus 96 Real-Time PCR System. |
| 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.
Inquiry
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