I-2019-nCoV/IAV/IBV Nucleic Acid Test Kit (PCR- fluorescence probe method)
Ukusetshenziswa Okuhlosiwe
Le khithi iwukuhlolwa kwesikhathi sangempela kwe-RT-PCR okuhloselwe ukutholwa kwekhwalithi ye-RNA kusukela ku-2019-nCoV, igciwane le-Influenza A (IAV), igciwane loMkhuhlane B (IBV).
Izinzuzo
Ukutholwa ngokubambisana:ukutholwa kwekhwalithi ye-RNA kusukela ku-2019-nCoV, i-Influenza A virus (IAV), igciwane le-Influenza B (IBV).
Ezokuthutha phakathi kuka-37 ℃ izinyanga ezingu-3:i-lyophilized reagent izinzile;Izimo zokuhamba: ≤37℃, zizinzile izinyanga ezi-3.
Ukusebenza okuncane:Isixazululo se-amplification reaction sahlanganiswa ndawonye, ukunciphisa ukusebenza kwelabhorethri.
Izinhlobo ezahlukene zesampula:Uhlobo lwesampula lwe-nasopharyngeal swab; i-oropharyngeal swabs; isikhwehlela; ama-alveolar lavage fluid specimens.
Ukusebenza Okuthembekile:Izinga lokuziqondana kwemikhiqizo yereferensi emihle noma engalungile: 100%.i-coefficient yokuhluka kwevelu ye-Ct (CV, %) ingaphansi noma ilingana no-5%.
Izinsimbi
I-UltraFast QPCR FQ-8A, i-QuantGene 9600 Real-Time PCR System ;I-ABI 7500 Real-Time PCR System, Roche LightCycler96 Real-Time PCR System, Tianlong TL988 Real-Time PCR System, SLAN Real-Time PCR System njll.
Kudingeka isiteshi se-fluorescent
Isiteshi sokutholwa kofuzo lwe-N: FAM
Isiteshi sokuthola i-IBV: VIC
Isiteshi sokuthola i-IAV: I-Tex Red
Isiteshi sokuthola ukulawula kwangaphakathi: CY5
Umkhawulo Wokutholwa
2019-nCoV : 400 amakhophi/mL.
Igciwane lomkhuhlane A: 1.5 TCID50/mL.
Igciwane lomkhuhlane B: 2.0 TCID50/mL.
Ukucaciswa kokuhlaziya
Le khithi yokuhlola ingasetshenziswa ukuthola i-2019-nCoV, igciwane loMkhuhlane A (2009 H1N1, H1N1,H3N2,H5N1, H7N9), igciwane Lomkhuhlane B (Yamagata, Victoria) ngokuqondile.
Ukucaciswa komkhiqizo
12X8T
12X4T
HS28- 12X8T/Kit
I-HS28- 4X24T/Kit