Fluorescence PCR · Sexually Transmitted Disease
Trichomonas vaginalis Detection Kit (Fluorescence PCR)
Qualitative detection of Trichomonas vaginalis nucleic acid in urogenital tract secretion samples for the diagnosis of trichomoniasis, a common sexually transmitted infection associated with increased risk of HIV and HPV.
- SKU Code
- On request
- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of Trichomonas vaginalis nucleic acid in urogenital tract secretion samples for the diagnosis of trichomoniasis, a common sexually transmitted infection associated with increased risk of HIV and HPV.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Sexually Transmitted Disease |
Epidemiology
Trichomonas vaginalis (TV) is a flagellate protozoan that inhabits the human vagina and urinary tract, primarily causing trichomonas vaginitis and urethritis, a sexually transmitted infection. The organism is highly resilient in the external environment and infects individuals universally. Globally, around 180 million people are infected, with the highest prevalence among women between 20 and 40 years of age. TV infection increases the risk of acquiring other pathogens, including human immunodeficiency virus (HIV) and human papillomavirus (HPV). Epidemiological data indicate strong associations between TV infection and adverse pregnancy outcomes, cervicitis, infertility, as well as the development and prognosis of reproductive tract malignancies such as cervical cancer and prostate cancer. Therefore, accurate detection of Trichomonas vaginalis infection is a critical step in disease management and is essential for controlling its transmission.
Reagent required but not provided
General DNA/RNA kit (usable with an automatic nucleic acid extractor) and nucleic acid extraction or purification kit (YDP302).
| SKU code | On request |
|---|---|
| Storage | Liquid: ≤-18℃ In dark |
| Shelf-life | 12 months |
| Specimen Type | urethral secretions, cervical secretions |
| Ct | ≤38 |
| CV | ＜5.0% |
| LoD | 400Copies/mL |
| Specificity | There is no cross-reactivity with other urogenital tract samples, such as Candida albicans, Chlamydia trachomatis, Ureaplasma urealyticum, Neisseria gonorrhoeae, Group B streptococcus, Mycoplasma hominis, Mycoplasma genitalium, Herpes simplex virus, Human papillomavirus, Escherichia coli, Gardnerella vaginalis, staphylococcus aureus and Human Genomic DNA, etc. |
| Applicable Instruments | It 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 |
| Approval | On request |
|---|---|
| Documents | Datasheet, 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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