Fluorescence PCR · Sexually Transmitted Disease
Chlamydia trachomatis, Ureaplasma urealyticum, and Neisseria gonorrhoeae Detection Kit (Fluorescence PCR)
Qualitative detection of Chlamydia trachomatis, Ureaplasma urealyticum, and Neisseria gonorrhoeae in urogenital specimens. For STD diagnosis.
- SKU Code
AENE-UR019A- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of Chlamydia trachomatis, Ureaplasma urealyticum, and Neisseria gonorrhoeae in urogenital specimens. For STD diagnosis.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Sexually Transmitted Disease |
Epidemiology
Sexually transmitted infections (STIs) continue to pose a significant risk to global public health, potentially causing infertility, preterm birth, cancer development, and other severe complications. The causative agents of STIs are diverse, encompassing bacteria, viruses, chlamydia, mycoplasma, and spirochetes. Frequently encountered pathogens include Neisseria gonorrhoeae, Chlamydia trachomatis, Ureaplasma urealyticum, herpes simplex virus types 1 and 2, Mycoplasma hominis, and Mycoplasma genitalium.
| SKU code | AENE-UR019A |
|---|---|
| Storage | Liquid: ≤-18℃ In dark; Lyophilized: ≤30℃ In dark |
| Shelf-life | 12 months |
| Specimen Type | Urethral secretions, cervical secretions |
| Ct | ≤38 |
| CV | ＜5.0% |
| LoD | Liquid: 400 Copies/mL; Lyophilized:400 Copies/mL |
| Specificity | There is no cross-reactivity for detecting other STD-infected pathogens, such as Treponema pallidum, etc. |
| 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 System 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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