Isothermal Amplification · Respiratory Infections
Mycoplasma pneumoniae Nucleic Acid Detection Kit (Isothermal Amplification)
For in vitro qualitative detection of Mycoplasma pneumoniae nucleic acid in human throat swabs.
- SKU Code
AENE-RT129A- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
For in vitro qualitative detection of Mycoplasma pneumoniae nucleic acid in human throat swabs.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Isothermal Amplification |
| Application area | Respiratory Infections |
Certificate
CE
Epidemiology
Mycoplasma pneumoniae (MP) is the smallest prokaryotic organism, possessing a cell structure but lacking a cell wall, and falls between bacteria and viruses. It primarily causes respiratory infections in humans, particularly in children and young adults. MP is responsible for various conditions such as pneumonia (including atypical pneumonia) and respiratory tract infections in children. Clinical presentations vary widely; the most frequent are severe cough, fever, chills, headache, sore throat, and upper respiratory infections, often leading to bronchopneumonia. Some patients may progress from an upper respiratory infection to severe pneumonia, which can result in acute respiratory distress and occasionally death. MP is a common and significant pathogen in community-acquired pneumonia (CAP), representing 10%–30% of cases; this proportion can rise 3- to 5-fold during outbreaks. Over recent years, the share of MP among CAP pathogens has steadily grown. The incidence of Mycoplasma pneumoniae infection is rising, and because its symptoms are nonspecific, it is easily mistaken for bacterial or viral colds. Consequently, early laboratory diagnosis is crucial for appropriate clinical management.
Work Flow
Option 1.
Recommended extraction reagents: a viral DNA/RNA kit and a nucleic acid extractor.
Option 2.
Recommended extraction reagent: a nucleic acid extraction or purification kit (e.g., YD315-R).
| SKU code | AENE-RT129A |
|---|---|
| Storage | Liquid: ≤-18℃ In dark, Lyophilized: ≤30℃ In dark |
| Shelf-life | Liquid: 9 months, Lyophilized: 12 months |
| Specimen Type | Throat swab |
| Tt | ≤28 |
| CV | ≤10.0% |
| LoD | 2 Copies/μL |
| Specificity | No cross-reactivity with other respiratory samples such as Influenza A, Influenza B, Legionella pneumophila, Rickettsia Q fever, Chlamydia pneumoniae, Adenovirus, Respiratory Syncytial Virus, Parainfluenza 1, 2, 3, Coxsackie virus, Echo virus, Metapneumovirus A1/A2/B1/B2, Respiratory syncytial virus A/B, Coronavirus 229E/NL63/HKU1/OC43, Rhinovirus A/B/C, Boca virus 1/2/3/4, Chlamydia trachomatis, adenovirus, etc. and human genomic DNA. |
| Applicable Instruments | Applied Biosystems 7500 Real-Time PCR Systems SLAN ®-96P Real-Time PCR Systems LightCycler® 480 Real-Time PCR system Easy Amp Real-time Fluorescence Isothermal Detection 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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