Isothermal Amplification · Sexually Transmitted Disease
Neisseria gonorrhoeae Detection Kit (Enzymatic Probe Isothermal Amplification)
Qualitative detection of Neisseria gonorrhoeae nucleic acid in genitourinary tract samples to aid in the diagnosis of gonococcal infection. Uses enzymatic probe isothermal amplification technology.
- SKU Code
- On request
- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of Neisseria gonorrhoeae nucleic acid in genitourinary tract samples to aid in the diagnosis of gonococcal infection. Uses enzymatic probe isothermal amplification technology.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Isothermal Amplification |
| Application area | Sexually Transmitted Disease |
Certificate
CE
Epidemiology
Gonorrhea is a well-known sexually transmitted infection resulting from Neisseria gonorrhoeae (NG). It primarily presents as purulent inflammation of the urogenital mucosal surfaces. According to WHO estimates from 2012, there were approximately 78 million adult cases globally. The pathogen colonizes the urogenital tract, leading to urethritis in males, and both urethritis and cervicitis in females. Inadequate treatment can allow the infection to extend into the reproductive organs. During childbirth, an infected mother may transmit the bacterium to the newborn, causing gonococcal ophthalmia neonatorum. Humans possess no inherent immunity against N. gonorrhoeae, so all individuals are susceptible. Furthermore, the immune response following infection is insufficient to prevent subsequent re-infections.
| SKU code | On request |
|---|---|
| Storage | Liquid: ≤-18℃ In dark; Lyophilized: ≤30℃ In dark |
| Shelf-life | Liquid: 9 months; Lyophilized: 12 months |
| Specimen Type | Urine for men, urethral swab for men, cervical swab for women |
| Tt | ≤28 |
| CV | ≤5.0% |
| LoD | 50pcs/mL |
| Specificity | No cross-reactivity with other genitourinary infection pathogens such as high-risk HPV type 16, human papillomavirus type 18, herpes simplex virus type 2, treponema pallidum, M.hominis, Mycoplasma genitalium, Staphylococcus epidermidis, Escherichia coli, Gardnerella vaginalis, Candida albicans, Trichomonas vaginalis, L.crispatus, adenovirus, cytomegalovirus, Group B Streptococcus, HIV virus, L.casei, and human genome DNA. |
| Applicable Instruments | Applied Biosystems 7500 Real-Time PCR Systems SLAN-96P Real-Time PCR Systems LightCycler®480 Real-Time PCR system Real-time Fluorescence Constant Temperature Detection System Easy Amp |
| 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.
Inquiry
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