Influenza A Virus/Influenza B Virus Nucleic Acid Test Kit (PCR-fluorescence probe method)
INTENDED USE
This kit is a lyophilized nucleic acid detection reagent, pre-packed in fluorescent PCR 8-strip tubes for the qualitative detection of Influenza A Virus/Influenza B Virus (IAV/IBV) nucleic acid in human oropharyngeal swabs and is suitable for the auxiliary diagnosis of Influenza A Virus/Influenza B Virus. Positive results indicate the presence of Influenza A Virus (IAV) or Influenza B Virus (IBV); clinical correlation with the patient's medical history and other diagnostic information is necessary to determine the patient's infection status. Positive results do not exclude bacterial infection or co-infection with other viruses. The pathogen detected may not be the exact cause of the disease.
Negative results do not exclude Influenza A Virus (IAV) or Influenza B Virus (IBV) infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical features, patient history, and epidemiological information to make clinical decisions.
This kit is intended for use by qualified and trained clinical laboratory personnel with specific training in PCR and in vitro molecular diagnostic procedure techniques.
This kit is for in vitro diagnostic use only.
APPLICABLE INSTRUMENTS
This test kit is applicable to be used with different kinds of PCR detection systems including UltraFast QPCR HC800, and regular Real-Time PCR Systems such as ABI 7500 Real-Time PCR System, Tianlong TL988 Real-Time PCR System, SLAN Real-Time PCR System.
SAMPLE REQUIREMENTS
Sample type: oropharyngeal swabs.
TRANSPORTATIONCONDITION
2°C ~3o°C, stable for 3 months.
INTENDED USE
This kit is a lyophilized nucleic acid detection reagent, pre-packed in fluorescent PCR 8-strip tubes for the qualitative detection of Influenza A Virus/Influenza B Virus (IAV/IBV) nucleic acid in human oropharyngeal swabs and is suitable for the auxiliary diagnosis of Influenza A Virus/Influenza B Virus. Positive results indicate the presence of Influenza A Virus (IAV) or Influenza B Virus (IBV); clinical correlation with the patient's medical history and other diagnostic information is necessary to determine the patient's infection status. Positive results do not exclude bacterial infection or co-infection with other viruses. The pathogen detected may not be the exact cause of the disease.
Negative results do not exclude Influenza A Virus (IAV) or Influenza B Virus (IBV) infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical features, patient history, and epidemiological information to make clinical decisions.
This kit is intended for use by qualified and trained clinical laboratory personnel with specific training in PCR and in vitro molecular diagnostic procedure techniques.
This kit is for in vitro diagnostic use only.
APPLICABLE INSTRUMENTS
This test kit is applicable to be used with different kinds of PCR detection systems including UltraFast QPCR HC800, and regular Real-Time PCR Systems such as ABI 7500 Real-Time PCR System, Tianlong TL988 Real-Time PCR System, SLAN Real-Time PCR System.
SAMPLE REQUIREMENTS
Sample type: oropharyngeal swabs.
TRANSPORTATIONCONDITION
2°C ~3o°C, stable for 3 months.
INTENDED USE
This kit is a lyophilized nucleic acid detection reagent, pre-packed in fluorescent PCR 8-strip tubes for the qualitative detection of Influenza A Virus/Influenza B Virus (IAV/IBV) nucleic acid in human oropharyngeal swabs and is suitable for the auxiliary diagnosis of Influenza A Virus/Influenza B Virus. Positive results indicate the presence of Influenza A Virus (IAV) or Influenza B Virus (IBV); clinical correlation with the patient's medical history and other diagnostic information is necessary to determine the patient's infection status. Positive results do not exclude bacterial infection or co-infection with other viruses. The pathogen detected may not be the exact cause of the disease.
Negative results do not exclude Influenza A Virus (IAV) or Influenza B Virus (IBV) infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical features, patient history, and epidemiological information to make clinical decisions.
This kit is intended for use by qualified and trained clinical laboratory personnel with specific training in PCR and in vitro molecular diagnostic procedure techniques.
This kit is for in vitro diagnostic use only.
APPLICABLE INSTRUMENTS
This test kit is applicable to be used with different kinds of PCR detection systems including UltraFast QPCR HC800, and regular Real-Time PCR Systems such as ABI 7500 Real-Time PCR System, Tianlong TL988 Real-Time PCR System, SLAN Real-Time PCR System.
SAMPLE REQUIREMENTS
Sample type: oropharyngeal swabs.
TRANSPORTATIONCONDITION
2°C ~3o°C, stable for 3 months.