STI Multiplex 7 Detection Kit (Fluorescence PCR)

Qualitative fluorescence PCR assay for the detection of seven common STI pathogens—Neisseria gonorrhoeae, Chlamydia trachomatis, Ureaplasma urealyticum, HSV-1, HSV-2, Mycoplasma hominis, and Mycoplasma genitalium—in male urinary tract and female genital tract secretions. Aids in the diagnosis of urogenital infections.

SKU Code
AENE-UR012
Approval
On request
Product Type
Assay / Kit
Status
Available

Qualitative fluorescence PCR assay for the detection of seven common STI pathogens—Neisseria gonorrhoeae, Chlamydia trachomatis, Ureaplasma urealyticum, HSV-1, HSV-2, Mycoplasma hominis, and Mycoplasma genitalium—in male urinary tract and female genital tract secretions. Aids in the diagnosis of urogenital infections.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaSexually Transmitted Disease

Epidemiology

Sexually transmitted infections (STIs) persist as a major global public health concern, potentially leading to infertility, preterm birth, tumorigenesis, and a range of serious complications. The spectrum of STI pathogens includes bacteria, viruses, chlamydia, mycoplasma, and spirochetes. Commonly encountered organisms are NG, CT, UU, HSV 1, HSV 2, Mh, and Mg.

SKU codeAENE-UR012
Storage≤ -18℃
Shelf-life12 months
Specimen TypeUrethral secretions, Cervical secretions
CV5.0%
LoDLimit of Detection (LoD): The LoD of the kit for detecting CT, NG, UU, HSV1, HSV2 and Mg is 400Copies/mL; the LoD of the kit for detecting Mh is 1000Copies/mL.
SpecificityThere is no cross reaction with similar STI pathogens.
Applicable InstrumentsApplied Biosystems 7500 Real-Time PCR Systems, Applied Biosystems 7500 Fast Real-Time PCR Systems, QuantStudio®5 Real-Time PCR systems, SLAN® -96P Real-Time PCR Systems, LightCycler® 480 Real-Time PCR system, LineGene 9600 Plus Real-Time PCR Detection System (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 Systemand and etc.
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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