Nine Kinds of Genitourinary Tract Infection Pathogen Nucleic Acid Detection Kit (Fluorescence PCR)

Qualitative detection of nine genitourinary pathogens—Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Mycoplasma hominis (Mh), Herpes Simplex Virus Type 1 (HSV1), Ureaplasma urealyticum (UU), Herpes Simplex Virus Type 2 (HSV2), Ureaplasma parvum (UP), Mycoplasma genitalium (Mg), and Trichomonas vaginalis (TV)—in urine, urethral, cervical, and vaginal swabs to aid diagnosis of genitourinary tract infections.

SKU Code
AENE-UR048
Approval
On request
Product Type
Assay / Kit
Status
Available

Qualitative detection of nine genitourinary pathogens—Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Mycoplasma hominis (Mh), Herpes Simplex Virus Type 1 (HSV1), Ureaplasma urealyticum (UU), Herpes Simplex Virus Type 2 (HSV2), Ureaplasma parvum (UP), Mycoplasma genitalium (Mg), and Trichomonas vaginalis (TV)—in urine, urethral, cervical, and vaginal swabs to aid diagnosis of genitourinary tract infections.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaSexually Transmitted Disease

Epidemiology

Sexually transmitted infections (STIs) pose a serious ongoing risk to global public health, contributing to infertility, preterm birth, cancer development, and a range of severe complications. STI-causing pathogens encompass bacteria, viruses, Chlamydia, Mycoplasma, and spirochetes. Commonly encountered agents include Chlamydia trachomatis, Ureaplasma urealyticum, Ureaplasma parvum, Mycoplasma hominis, herpes simplex virus type 1 (HSV-1), Neisseria gonorrhoeae, herpes simplex virus type 2 (HSV-2), Mycoplasma genitalium, and Trichomonas vaginalis.

Work flow

Type I :

Type II:

SKU codeAENE-UR048
Storage≤ -18℃
Shelf-life12 months
Specimen TypeUrine, male urethral swab, female cervical swab, female vaginal swab
CV5.0%
LoDLimit of Detection (LoD): The LoD of the kit for detecting CT, NG, UU, UP, HSV1, HSV2, Mg, and TV is 400Copies/mL; the LoD of the kit for detecting Mh is 1000Copies/mL.
SpecificityThere is no cross reaction with similar STI pathogens.
Applicable InstrumentsType I: Applied Biosystems 7500 Real-Time PCR System, Applied Biosystems 7500 Fast Real-Time PCR Systems, QuantStudio®5 Real-Time PCR Systems, SLAN-96P Real-Time PCR Systems (Hongshi Medical Technology Co. Ltd.), LightCycler®480 Real-Time PCR system, LineGene 9600 Plus Real-Time PCR Detection System (FQD-96A, Hangzhou Bioer technology) and MA-6000 Real-Time Quantitative Thermal Cycler (Suzhou Molarray Co. Ltd.). Ltd. Type II:
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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