Optimization of DNase I Removal of Contaminating DNA from RNA for Use in Quantitative RNA-PCR

In competitive RNA-PCR studies, contaminating DNA can produce incorrect results because of its potential to act as a second competitor. Preliminary studies using published methods for DNase I digestion of DNA as a contaminant of RNA, followed by thermal inactivation of the enzyme at 95°C for 5 min b...

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Bibliographic Details
Main Authors: Zeqi Huang, Michael J. Fasco, Laurence S. Kaminsky
Format: Article
Language:English
Published: Taylor & Francis Group 1996-06-01
Series:BioTechniques
Online Access:https://www.future-science.com/doi/10.2144/96206st02
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