HIV Quantitative Detection Kit (Fluorescence PCR)

This fluorescence PCR kit quantitatively detects HIV RNA in human serum/plasma for viral load monitoring.

SKU Code
AENE-OT032
Approval
On request
Product Type
Assay / Kit
Status
Available

This fluorescence PCR kit quantitatively detects HIV RNA in human serum/plasma for viral load monitoring.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaSexually Transmitted Disease

Certificate

CE

Epidemiology

HIV lives in human blood and compromises the immune system, leaving the body vulnerable to other diseases. This can lead to untreatable infections and tumors, which may be fatal. Transmission occurs through sexual contact, blood, and from mother to child.

Work Flow

Recommended extraction reagent: Virus DNA/RNA Kit (suitable for use with an Automatic Nucleic Acid Extractor). Conduct the extraction as per the instruction manual. Use a sample volume of 300 μL and elute with 80 μL.

SKU codeAENE-OT032
Storage≤-18℃ In dark
Shelf-life9 months
Specimen TypeSerum/Plasma samples
CV≤5.0%
Ct≤38
LoD100 IU/mL
SpecificityUse the kit to test other virus or bacterial samples such as: human cytomegalovirus, EB virus, human immunodeficiency virus, hepatitis B virus, hepatitis A virus, syphilis, herpes simplex virus type 1, herpes simplex virus type 2, influenza A virus, staphylococcus aureus, candida albicans, etc. and the results are all negative.
Applicable Instruments: Applied Biosystems 7500 Real-Time PCR Systems Applied Biosystems 7500 Fast Real-Time PCR Systems SLAN ®-96P Real-Time PCR Systems QuantStudio™ 5 Real-Time PCR Systems LightCycler®480 Real-Time PCR system LineGene 9600 Plus Real-Time PCR Detection System MA-6000 Real-Time Quantitative Thermal Cycler BioRad CFX96 Real-Time PCR System BioRad CFX Opus 96 Real-Time PCR System
ApprovalOn request
DocumentsDatasheet, 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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