Mycoplasma hominis Nucleic Acid Detection Kit (Fluorescence PCR)

Qualitatively detects Mycoplasma hominis in male urinary tract and female genital tract secretions via fluorescence PCR, aiding the diagnosis of sexually transmitted infections.

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

Qualitatively detects Mycoplasma hominis in male urinary tract and female genital tract secretions via fluorescence PCR, aiding the diagnosis of sexually transmitted infections.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaSexually Transmitted Disease

Epidemiology

Sexually transmitted infections continue to be a major global health concern, associated with infertility, preterm delivery, carcinogenesis, and other severe sequelae. Mycoplasma hominis (MH) colonizes the urogenital tract and triggers local inflammation. In men, urogenital MH infection can manifest as non-gonococcal urethritis and epididymitis; in women, it often causes a cervicitis-centered reproductive inflammation that may ascend, frequently leading to salpingitis, and occasionally resulting in endometritis and pelvic inflammatory disease.

SKU codeOn request
StorageLiquid: ≤-18℃ In dark
Shelf-life12 months
Specimen Typeurethral secretions, cervical secretions
Ct≤38
CV<5.0%
LoD1000Copies/mL
SpecificityThere is no cross-reactivity with other STD infection pathogens, which are outside the detection range, and there is no cross-reactivity with chlamydia trachomatis, ureaplasma urealyticum, neisseria gonorrhoeae, mycoplasma genitalium, herpes simplex virus type 1, herpes simplex virus type 2, etc.
Applicable InstrumentsIt can match the mainstream fluorescent PCR instruments on the market. 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 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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