IAV/IBV/ADV Nucleic Acid Test Kit (PCR- fluorescence probe method)
Contact us for pricing - info@breakwatersci.com
For research use only
PRODUCT NAME
IAV/IBV/ADV Nucleic Acid Test Kit (PCR- fluorescence probe method)
PACKAGE SPECIFICATION
48T/Kit
INTENDED USE
This kit is intended for in vitro qualitative detection of Influenza A virus (IAV), Influenza B virus (IBV) and Human adenovirus (ADV) nucleic acid in human oropharyngeal swabs specimens.
Influenza A virus, influenza B virus and Human adenovirus can all cause respiratory tract infections with similar clinical symptoms, mainly fever, cough, nasal congestion, throat discomfort, fatigue, headache, muscle aches and other symptoms, and some patients are accompanied by shortness of breath, bronchitis or pneumonia.
This kit is suitable for the auxiliary diagnosis of IAV/IBV/ADV infection, clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Negative results must be combined with clinical observations, patient history, and epidemiological information to make decision.
This kit is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro molecular diagnostic procedures.
This kit is for in vitro diagnostic use only.
Contact us for pricing - info@breakwatersci.com
For research use only
PRODUCT NAME
IAV/IBV/ADV Nucleic Acid Test Kit (PCR- fluorescence probe method)
PACKAGE SPECIFICATION
48T/Kit
INTENDED USE
This kit is intended for in vitro qualitative detection of Influenza A virus (IAV), Influenza B virus (IBV) and Human adenovirus (ADV) nucleic acid in human oropharyngeal swabs specimens.
Influenza A virus, influenza B virus and Human adenovirus can all cause respiratory tract infections with similar clinical symptoms, mainly fever, cough, nasal congestion, throat discomfort, fatigue, headache, muscle aches and other symptoms, and some patients are accompanied by shortness of breath, bronchitis or pneumonia.
This kit is suitable for the auxiliary diagnosis of IAV/IBV/ADV infection, clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Negative results must be combined with clinical observations, patient history, and epidemiological information to make decision.
This kit is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro molecular diagnostic procedures.
This kit is for in vitro diagnostic use only.
Contact us for pricing - info@breakwatersci.com
For research use only
PRODUCT NAME
IAV/IBV/ADV Nucleic Acid Test Kit (PCR- fluorescence probe method)
PACKAGE SPECIFICATION
48T/Kit
INTENDED USE
This kit is intended for in vitro qualitative detection of Influenza A virus (IAV), Influenza B virus (IBV) and Human adenovirus (ADV) nucleic acid in human oropharyngeal swabs specimens.
Influenza A virus, influenza B virus and Human adenovirus can all cause respiratory tract infections with similar clinical symptoms, mainly fever, cough, nasal congestion, throat discomfort, fatigue, headache, muscle aches and other symptoms, and some patients are accompanied by shortness of breath, bronchitis or pneumonia.
This kit is suitable for the auxiliary diagnosis of IAV/IBV/ADV infection, clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Negative results must be combined with clinical observations, patient history, and epidemiological information to make decision.
This kit is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro molecular diagnostic procedures.
This kit is for in vitro diagnostic use only.