Le khithi ifanele ukutholwa kwekhwalithi yegciwane le-hepatitis E (HEV) i-nucleic acid kumasampula e-serum kanye namasampula endle ku-vitro.
Le khithi ifanele ukutholwa kwekhwalithi yegciwane le-hepatitis A (HAV) i-nucleic acid kumasampula e-serum kanye namasampula endle ku-vitro.
Le khithi isetshenziselwa ukutholwa kwe-in vitro quantitative ye-RNA yegciwane le-hepatitis B kusampula seserum yomuntu.
Le kit isetshenziselwa ukutholwa komthamo wegciwane le-hepatitis B nucleic acid ku-serum yomuntu noma amasampula e-plasma.
Le kit isetshenziselwa ukutholwa kwe-genotyping yegciwane le-hepatitis C (HCV) subtypes 1b, 2a, 3a, 3b kanye no-6a kumasampula omtholampilo we-serum/plasma yegciwane le-hepatitis C (HCV).Isiza ekuxilongeni nasekwelapheni iziguli ze-HCV.
I-HCV Quantitative Real-Time PCR Kit iyi-in vitro Nucleic Acid Test (NAT) ukuze ithole futhi ilinganise ama-nucleic acid e-Hepatitis C Virus (HCV) ku-plasma yegazi lomuntu noma amasampula e-serum ngosizo lwe-Quantitative Real-Time Polymerase Chain Reaction (qPCR ) indlela.
Le khithi isetshenziselwa ukutholwa kokuthayipha kwekhwalithi yohlobo B, uhlobo C kanye nohlobo D kumasampula e-serum/plasma egciwane le-hepatitis B (HBV)
Le kit isetshenziselwa ukutholwa kwe-in vitro quantitative ye-hepatitis B virus nucleic acid kumasampula e-serum yomuntu.