Fluorescence PCR · Sexually Transmitted Disease
Chlamydia Trachomatis Nucleic Acid Detection Kit (Fluorescence PCR)
Qualitative detection of Chlamydia trachomatis nucleic acid in male urine, male urethral swab, and female cervical swab specimens via fluorescence PCR.
- SKU Code
- On request
- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of Chlamydia trachomatis nucleic acid in male urine, male urethral swab, and female cervical swab specimens via fluorescence PCR.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Sexually Transmitted Disease |
Intended Use
The kit is designed for the qualitative detection of Chlamydia trachomatis nucleic acid in specimens including male urine, male urethral swabs, and female cervical swabs.
Epidemiology
Chlamydia trachomatis (CT) is an obligate intracellular prokaryotic parasite. It is classified into serotypes A through K based on serological methods. Urogenital infections are predominantly caused by the trachoma biovar serotypes D–K. In men, CT typically presents as urethritis, which may resolve spontaneously but often becomes chronic with periodic exacerbations, and can be associated with epididymitis, proctitis, and other conditions. In women, infection can result in urethritis, cervicitis, and, more seriously, salpingitis.
Epidemiology
The FAM channel detects Chlamydia trachomatis (CT), while the VIC/HEX channel detects the internal control.
| SKU code | On request |
|---|---|
| Storage | ≤-18℃ In dark |
| Shelf-life | 12 months |
| Specimen Type | Male urethral secretions, Female cervical secretions, Male urine |
| Ct | ≤38 |
| CV | ＜5.0% |
| LoD | 400Copies/mL |
| Specificity | There is no cross-reactivity for detecting other STD-infected pathogens by this kit, such as Treponema pallidum, Neisseria gonorrhoeae, Ureaplasma urealyticum, Mycoplasma hominis, Mycoplasma genitalium, etc. which are outside the detection range of kit. |
| Applicable Instruments | It can match the mainstream fluorescent PCR instruments on the market. Applied Biosystems 7500 Real-Time PCR Systems 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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