Ezplex Respiratory Pathogens Real-time PCR Kit is an in vitro diagnostic test for the qualitative detection of 19 respiratory viruses and 6 types of pneumonia-causing bacteria through nucleic acids isolated and extracted from human throat swabs using real-time polymerase chain reaction
Comprehensive Panel- One test can identify 19 respiratory viruses and 6 bacterial species simultaneously.
Sensitivity Detection of all targeted viruses and bacteria with high sensitivity.
Convenience Genetree Viewer analysis software available for users to conveniently produce test results.
Clinical Performance: Clinical testing confirmed the high sensitivity and specificity.
Stability: Shelf life of up to 12 months.
Analytical Specificity: Testing of 31 species of microorganisms showed no cross reactivity.
Temperature Block Temperature Range: 0 - 105 Max. Heating Rate: 7 /s Max. Cooling Rate: 5 /s
Ezple Respiratory Pathogens Real-time PCR Kit is an in vitro diagnostic test for the qualitative detection of 19 respiratory viruses and 6 types of pneumonia-causing bacteria through nucleic acids isolated and extracted from human throat swabs using real-time polymerase chain reaction.
2X Real-Time PCR Master Mix including SYBR Green in Mixture 2X HRM Master mix
This kit is intended for qualiativein vitro detection of Orf1ab and N genes of Novel Coronavirus 2019-nCoV which are found in throat swab,sputum and alveolar lavage fuid samples of suspected cases of pneumonia,suspected cases of clustering and other patients who need to carry out diagnosis or differential diagnosis of Novel Coronavirus 2019-nCoV infection.
Monkeypox Virus Real-time PCR Kit. PM for details.
DESCRIPTION * Detection of Sars-Cov-2 with reverse transcption Real time PCR ( TAT 2.0 hr ) * Amplify N gene and RdRp(orf1ab) gene of Sars-Cov2 AVAILABLE SAMPLE TYPE * Sputum * Oropharyngeal ( OP ) and nasopharyngeal ( NP ) swabs
SFTS Virus Real-time PCR Kit is an in vitro diagnostic test intended for the qualitative detection of the Dabie bandavirus that causes Severe Fever with thrombocytopenia Syndrome using nucleic acid RNA extracted from human blood or serum. Clinical evaluation performed with human blood specimens confirmed clinical accuracy. High reproducibility with similar results were confirmed various tests.
Lowest detection line:200 copy/ml CE marks
25 tests per box
