Extraction and isolation of viral RNA is the first step in the detection and testing of viral RNA by real-time RT-PCR. Here we compare different methods and protocols for extraction of viral RNA.
Nested RT-PCR and real-time RT-PCR are the most common methods for the analysis of viral infections (see Robert Koch Institute >). In contrast to examinations with ELISA or IFA, this can be done at an earlier stage of infection.
Nested RT-PCR and real-time RT-PCR are the most common methods for the analysis of viral infections (see Robert Koch Institute >). In contrast to examinations with ELISA or IFA, this can be done at an earlier stage of infection.
Die Extraktion und Isolation viraler RNA ist der erste Schritt zum Nachweis und Test von Virus-RNA über real-time RT-PCR. Wir stellen hier verschiedene Methoden und Protokolle zur Extraktion viraler RNA vor.
A special regulatory strategy of genome translation in RNA viruses and bacterias is mediated via RNA thermometers. RNA thermometers (RNATs) are secondary structures in RNA sequences that are essential for the virulence of the organism. However the base pairing in the RNA thermometers can be altered due to various factors like the thermal denaturation.
A special regulatory strategy of genome translation in RNA viruses and bacterias is mediated via RNA thermometers. RNA thermometers (RNATs) are secondary structures in RNA sequences that are essential for the virulence of the organism. However the base pairing in the RNA thermometers can be altered due to various factors like the thermal denaturation.
A special regulatory strategy of genome translation in RNA viruses and bacterias is mediated via RNA thermometers. RNA thermometers (RNATs) are secondary structures in RNA sequences that are essential for the virulence of the organism. However the base pairing in the RNA thermometers can be altered due to various factors like the thermal denaturation.