14 Respiratory Pathogens Detection Kit (Fluorescence PCR)

In vitro qualitative detection of 14 respiratory pathogens: SARS-CoV-2, influenza A, influenza B, respiratory syncytial virus, adenovirus, human metapneumovirus, rhinovirus, parainfluenza 1–4, coronavirus, enterovirus, human bocavirus, Mycoplasma pneumoniae, Chlamydia pneumoniae, and Streptococcus pneumoniae, in oropharyngeal and nasopharyngeal swabs.

SKU Code
AENE-RT159B
Approval
On request
Product Type
Assay / Kit
Status
Available

In vitro qualitative detection of 14 respiratory pathogens: SARS-CoV-2, influenza A, influenza B, respiratory syncytial virus, adenovirus, human metapneumovirus, rhinovirus, parainfluenza 1–4, coronavirus, enterovirus, human bocavirus, Mycoplasma pneumoniae, Chlamydia pneumoniae, and Streptococcus pneumoniae, in oropharyngeal and nasopharyngeal swabs.

Product typeAssay / Kit
Technology platformFluorescence PCR
Application areaRespiratory Infections

Epidemiology

Infections of the respiratory tract represent the most prevalent human illness, affecting individuals regardless of gender, age, or geographic location. These infections are a major contributor to global morbidity and mortality[1]. Frequently encountered respiratory pathogens encompass the novel coronavirus, Influenza A and B viruses, Respiratory syncytial virus, Adenovirus, human metapneumovirus, rhinovirus, Parainfluenza virus types I through IV, Bocavirus, Enterovirus, Coronavirus, Mycoplasma pneumoniae, Chlamydia pneumoniae, and Streptococcus pneumoniae [2,3].

Work Flow

The suggested extraction reagent is the Viral DNA/RNA Kit, compatible with an Automatic Nucleic Acid Extractor. Use a sample volume of 200 µL for extraction. All further steps must follow the reagent’s instructions for use. The advised elution volume is 80 µL.

SKU codeAENE-RT159B
Storage≤-18℃
Shelf-life9 months
Specimen TypeOropharyngeal swab、Nasopharyngeal swab
Ct≤38
CV5.0%
LoD2 00Copies/mL
SpecificityThe cross-reactivity test results showed that there was no cross reaction between this kit and Cytomegalovirus, Herpes simplex virus type 1, Varicella-zoster virus, Epstein-Barr virus, Bordetella pertussis, Corynebacterium, Escherichia coli, Haemophilus influenzae, Lactobacillus, Legionella pneumophila, Moraxella catarrhalis, attenuated strains of Mycobacterium tuberculosis, Neisseria meningitidis, Neisseria, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pyogenes, Streptococcus salivarius, Acinetobacter baumannii, Stenotrophomonas maltophilia, Burkholderia cepacia, Corynebacterium striatum, Nocardia, Serratia marcescens, Citrobacter, Cryptococcus, Aspergillus fumigatus, Aspergillus flavus, Pneumocystis jiroveci, Candida albicans, Rothia mucilaginosus, Streptococcus oralis, Klebsiella pneumoniae, Chlamydia psittaci, Coxiella burnetii and human genomic nucleic acids.
Applicable InstrumentsSLAN-96P Real-Time PCR Systems (Hongshi Medical Technology Co. Ltd.) Applied Biosystems 7500 Real-Time PCR Systems Applied Biosystems 7500 Fast Real-Time PCR Systems QuantStudio ® 5 Real-Time PCR Systems 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
ApprovalOn request
DocumentsDatasheet, 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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