Ureaplasma Parvum Nucleic Acid Detection Kit (Fluorescence PCR)

Qualitative detection of Ureaplasma parvum DNA in male urine and female reproductive tract secretions to aid in the diagnosis of Ureaplasma parvum infections.

SKU Code
AENE-EQ011
Approval
On request
Product Type
Assay / Kit
Status
Available

Qualitative detection of Ureaplasma parvum DNA in male urine and female reproductive tract secretions to aid in the diagnosis of Ureaplasma parvum infections.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaSexually Transmitted Disease

Epidemiology

Human Ureaplasma pathogens are classified into two biogroups comprising 14 serotypes. Biogroup I, Ureaplasma urealyticum, encompasses serotypes 2, 4, 5, 7, 8, 9, 10, 11, 12, and 13. Biogroup II, Ureaplasma parvum, includes serotypes 1, 3, 6, and 14. Often a commensal or parasite in the lower female genital tract, Ureaplasma is a significant cause of genitourinary infections. Infected women frequently transmit the organism to sexual partners. Ureaplasma infection is an important contributor to infertility. In pregnancy, infection may result in preterm rupture of membranes, preterm delivery, neonatal respiratory distress syndrome, postpartum infection, and other serious adverse outcomes that warrant careful attention.

Reagent required but not provided

Normal saline and a Viral DNA/RNA Kit (compatible with an Automatic Nucleic Acid Extractor).

SKU codeAENE-EQ011
Storage-18℃
Shelf-life12 months
Specimen Typemale urinary tract,female reproductive tract
Ct≤38
CV<5.0%
LoD400 Copies/mL
Applicable InstrumentsApplicable to type I detection reagent: Applied Biosystems 7500 Real-Time PCR Systems, QuantStudio ® 5 Real-Time PCR Systems, SLAN-96P Real-Time PCR Systems (Hongshi Medical Technology Co. Ltd.), LineGene 9600 Plus Real-Time PCR Detection Systems (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 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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