Ureaplasma Urealyticum Nucleic Acid Detection Kit (Isothermal Amplification)

Qualitative detection of Ureaplasma urealyticum nucleic acid in genitourinary tract specimens. For in vitro diagnostic use in identifying urogenital infections caused by this pathogen.

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

Qualitative detection of Ureaplasma urealyticum nucleic acid in genitourinary tract specimens. For in vitro diagnostic use in identifying urogenital infections caused by this pathogen.

Product typeAssay / Kit
Technology platformIsothermal Amplification
Application areaSexually Transmitted Disease

Certificate

CE

Epidemiology

Ureaplasma urealyticum (UU) is the tiniest prokaryote capable of independent existence, positioned between bacteria and viruses, and is a common cause of genitourinary infections. In males, it may lead to conditions such as prostatitis, urethritis, and pyelonephritis. In females, it can trigger vaginal inflammation, cervicitis, and pelvic inflammatory disease. UU is among the pathogens associated with infertility and miscarriage. The species includes 14 serotypes, classified by molecular traits into two biogroups: Biogroup I (Up) contains four serotypes (1, 3, 6, and 14) with smaller genomes, while Biogroup II (Uu) encompasses the other ten serotypes, which have larger genomes.

SKU codeOn request
StorageLiquid: ≤-18℃ In dark; Lyophilized: ≤30℃ In dark
Shelf-lifeLiquid: 9 months; Lyophilized: 12 months
Specimen TypeUrine for men, urethral swab for men, cervical swab for women
Tt≤28
CV≤5.0%
LoD400Copies/mL
SpecificityThere is no cross-reactivity between this kit and High-risk HPV 16, HPV 18, Herpes simplex virus type 2, Treponema pallidum, Mycoplasma hominis, Mycoplasma genitalium, Staphylococcus epidermidis, Escherichia coli, Gardnerella vaginalis, Candida albicans, Trichomonas vaginalis, Lactobacillus crispatus, Adenovirus, Cytomegalovirus, Beta Streptococcus, HIV virus, Lactobacillus casei and human genomic DNA.
Applicable InstrumentsSample Release Reagent Viral DNA/RNA Kit () Automatic Nucleic Acid Extractor
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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