## Abstract Hepatitis C virus (HCV) requires reverse transcriptase‐polymerase chain reaction (RT‐PCR) or branched DNA signal amplification assays to be detected in patient samples. Although conventional methods of RNA isolation are employed for samples of serum, plasma, and peripheral blood mononuc
Rapid detection of hepatitis C virus RNA by direct capture from blood
✍ Scribed by Leen-Jan van Doom; Bernhard Kleter; Jolanda Voermans; Geert Maertens; Hans Brouwer; Ruud Heijtink; Wim Quint
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 753 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0146-6615
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A new diagnostic assay for hepatitis C virus RNA detection is described. HCV genomic RNA is captured onto streptavidin‐coated magnetic beads by solution hybridization with biotinylated complementary oligonucleotides. The specificity of the capture assay is confirmed using different capture oligonucleotides as well as sera representing different types of HCV. Sensitivity was determined by testing serial dilutions of a HCV infected plasma. A panel of 50 sera was tested for anti‐HCV by a Line Immunoassay and for HCV‐RNA by both a conventional guanidinium extraction method and the new capture assay. The specificity of the capture assay was 95.8% and the sensitivity was 92.3% compared to the standard protocol. This method provides a rapid and simple alternative for HCV‐RNA detection in blood samples. © 1994 Wiiey‐Liss, Inc.
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