Fluorescence PCR · Sexually Transmitted Disease
Mycoplasma Genitalium (Mg) Detection Kit (Fluorescence PCR)
Qualitative detection of Mycoplasma genitalium (Mg) nucleic acid in male urinary tract and female genital tract secretions. Intended as an aid in the diagnosis of Mg-related urogenital infections.
- SKU Code
- On request
- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of Mycoplasma genitalium (Mg) nucleic acid in male urinary tract and female genital tract secretions. Intended as an aid in the diagnosis of Mg-related urogenital infections.
| 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, contributing to infertility, premature birth, tumor development, and numerous other severe complications [1-4]. A wide variety of pathogens cause STIs, such as bacteria, viruses, chlamydia, mycoplasma, and spirochetes. Frequently encountered species include Neisseria gonorrhoeae, Chlamydia trachomatis, Ureaplasma urealyticum, herpes simplex virus types 1 and 2, Mycoplasma hominis, and Mycoplasma genitalium.
| SKU code | On request |
|---|---|
| Storage | -18℃ |
| Shelf-life | 12 months |
| Specimen Type | u rethral secretion, cervical secretions |
| Tt | ≤38 |
| CV | ≤5.0% |
| LoD | 500 Copies/μL |
| Specificity | There is no cross-reactivity with other sexually transmitted disease pathogens, such as Chlamydia trachomatis, Ureaplasma urealyticum, Neisseria gonorrhoeae, Mycoplasma hominis, Herpes simplex virus type 1, and Herpes simplex virus type 2. |
| Applicable Instruments | Applied Biosystems 7500 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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