Highly efficient, automated purification of viral DNA from human plasma
T7 phage DNA was spiked into human plasma samples. Viral DNA was purified in an automated manner by using the NucleoMag®Virus kit on the epMotion 5073m workstation. The recovery efficiency was determined by a subsequent Taqman® Probe qPCR assay using the Applied Biosystems® 7500 Real-Time PCR System.
Highly efficient, automated purification of viral RNA from human plasma
MS2 phage RNA was spiked into human plasma samples. Viral RNA was purified in an automated manner by using the NucleoMag®Virus kit on the epMotion 5073m workstation. The recovery efficiency was determined by a subsequent Taqman® Probe qRT-PCR assay using the Applied Biosystems® 7500 Real-Time PCR System.
Highly efficient, automated purification of viral DNA from human plasma
T7 phage DNA was spiked into human plasma samples. Viral DNA was purified in an automated manner by using the NucleoMag®Virus kit on the epMotion 5073m workstation. The recovery efficiency was determined by a subsequent Taqman® Probe qPCR assay using the Applied Biosystems® 7500 Real-Time PCR System.
Highly efficient, automated purification of viral RNA from human plasma
MS2 phage RNA was spiked into human plasma samples. Viral RNA was purified in an automated manner by using the NucleoMag®Virus kit on the epMotion 5073m workstation. The recovery efficiency was determined by a subsequent Taqman® Probe qRT-PCR assay using the Applied Biosystems® 7500 Real-Time PCR System.