## Abstract Rapid diagnosis of human herpesvirus primary infections or reactivations is facilitated by quantitative PCRs. Quantitative PCR assays with a standard thermal cycling profile permitting simultaneous detection of herpes simplex virus (HSV), varicella zoster virus (VZV), cytomegalovirus (C
โฆ LIBER โฆ
The optimization and validation of the glycoprotein ELISA assay for quantitative varicella-zoster virus (VZV) antibody detection
โ Scribed by Olivia Hammond; Yue Wang; Tina Green; Joseph Antonello; Robert Kuhn; Clifford Motley; Philip Stump; Beverly Rich; Narendra Chirmule; Rocio D. Marchese
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 251 KB
- Volume
- 78
- Category
- Article
- ISSN
- 0146-6615
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Rapid quantitative PCR assays for the si
โ
I. Engelmann; D.R. Petzold; A. Kosinska; B.G. Hepkema; T.F. Schulz; A. Heim
๐
Article
๐
2008
๐
John Wiley and Sons
๐
English
โ 155 KB
๐ 1 views
Validation of single real-time TaqManยฎ P
โ
V. Enouf; G. Dos Reis; J.P. Guthmann; P.J. Guerin; M. Caron; V. Marechal; E. Nic
๐
Article
๐
2006
๐
John Wiley and Sons
๐
English
โ 205 KB
๐ 1 views
Since the characterization of the genome of the hepatitis E virus (HEV) in 1990, a large genetic diversity has been described. A single real-time reverse transcription (RT)-PCR assay with TaqMan technology has been validated which uses only one set of primers and probe within the ORF2 HEV region (nt