Your Cart

Respiratory Pathogen Panel (RPP)

Respiratory Pathogen Panel (RPP)
Secured Shopping
Best security features
Respiratory Pathogen Panel (RPP)

Respiratory tract infections (RTIs) are very common in all age groups. As a large number of pathogens cause respiratory infection including both viruses and bacteria, knowledge of the etiology of an RTI is essential to facilitate the appropriate treatment of patients and reduces the inappropriate use of drugs.

The diagnosis methods of identifying pathogens in respiratory secretions specimens have been developed over many years. Initially, cell cultures, immunofluorescence assays, and rapid antigen direct tests were all used in identifying RTI pathogens. However, none of those methods are ideal for clinical use as they are either expensive, lack of sensitivity and specificity, or have a long turnaround time.

In recent years, those problems have been overcome with advanced molecular diagnostic methods in clinical use. FDA 510(k) Cleared Respiratory Pathogen Panel (RPP) is capable of the simultaneous detection and identification of nucleic acids from multiple viruses and bacteria extracted from nasopharyngeal swab (NPS) samples obtained from individuals with signs and/or symptoms of respiratory tract infection. This fully automated system can process up to 94 patient samples simultaneously. Thereby,  RPP can provide appropriate results to physicians within a short turnaround time (24-48 hours after sample receiving, or the same day if it's STAT case. ) to aid RTI pathogen diagnosis.

17 pathogens identified:


▪Influenza A

Subtype H1

Subtype H1 2009pdm

Subtype H3

▪Influenza B

▪Parainfluenza 1

▪Parainfluenza 2

▪Parainfluenza 3

▪Parainfluenza 4

▪Respiratory Syncytial Virus A and B

▪Human Metapneumovirus A and B


▪Coronavirus (229E, OC43, HKU1, and NL63) 



▪Mycoplasma pneumoniae

▪Chlamydia pneumoniae

▪Bordetella pertussis

Please review our Terms and Conditions, including Cancellation Policy (including 15% cancellation fee), Informed Consent.  By submitting this order, you certify that you have reviewed, understood, and agreed to the Terms and Conditions.  

When checking out, please do not refresh your web page, or submit the order multiple times, to avoid duplicate charges.  In the case of technical difficulties, please contact our customer service.  Please include the name, gender,  and birthday information for the people to be tested in the Comment area of the order.