Fluorescence PCR · Respiratory Infections
Chlamydia pneumoniae Nucleic Acid Detection Kit (Fluorescence PCR)
Qualitative detection of Chlamydia pneumoniae nucleic acid in human sputum and oropharyngeal swabs, aiding in the diagnosis of respiratory infections.
- SKU Code
AENE-RT023- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of Chlamydia pneumoniae nucleic acid in human sputum and oropharyngeal swabs, aiding in the diagnosis of respiratory infections.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Fluorescence PCR |
| Application area | Respiratory Infections |
Epidemiology
Acute respiratory tract infections (ARTIs) are frequent multifaceted illnesses in pediatrics. Chlamydia pneumoniae and Mycoplasma pneumoniae are two prevalent bacterial causes, exhibiting contagiousness and transmissibility via respiratory droplets. Affected individuals typically present with mild symptoms such as sore throat, nonproductive cough, and fever; children of any age can be susceptible. Comprehensive data indicate that school-aged children above 8 years and young adults represent the primary populations for Chlamydia pneumoniae infection, constituting roughly 10–20% of community-acquired pneumonia cases. Older adults with weakened immune systems or pre-existing conditions are also vulnerable. Over recent years, the incidence of Chlamydia pneumoniae infection has risen steadily, with particularly elevated rates among preschool and school-aged children. Because early symptoms are often atypical and the incubation period is prolonged, misdiagnosis and underdiagnosis are common in clinical settings, potentially delaying treatment for pediatric patients.
Work Flow
The Viral DNA/RNA Kit is available in two versions: one for use with the Automatic Nucleic Acid Extractor, and another for manual workflows. A sample volume of 200 µL is used for extraction, with a recommended elution volume of 150 µL.
| SKU code | AENE-RT023 |
|---|---|
| Storage | ≤-18℃ |
| Shelf-life | 12 months |
| Specimen Type | sputum,oropharyngeal swab |
| CV | ≤10.0% |
| LoD | 200Copies/mL |
| Specificity | The cross-reactivity test results showed that there was no cross reaction between this kit and Ureaplasma urealyticum, Mycoplasma genitalium, Mycoplasma hominis, Streptococcus pneumoniae, Mycoplasma pneumoniae, Haemophilus influenzae, Klebsiella pneumoniae, Staphylococcus aureus, Mycobacterium tuberculosis, Legionella pneumophila, Pseudomonas aeruginosa, Acinetobacter baumannii, influenza A virus, influenza B virus, Parainfluenza virus type I/II/III/IV, Rhinovirus, Adenovirus, human metapneumovirus, respiratory syncytial virus and human genomic nucleic acids |
| Applicable Instruments | 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 (Hongshi Medical Technology Co. Ltd.), LightCycler ® 480 Real-Time PCR system, LineGene 9600 Plus Real-Time PCR Detection Systems (FQD-96A, Hangzhou Bioer technology), MA-6000 Real-Time Quantitative Thermal Cycler (Suzhou Molarray Co. Ltd.), 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.
Inquiry
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