Abstract
A simple way to determine the amount of RNA made by in vitro transcription is to include a trace amount of radioactive nucleotide and calculate the amount of nucleotides incorporated into the RNA, as described here. This protocol can also be used to quantitate unlabeled transcripts, assuming that the unlabeled RNA is equivalent to an aliquot of labeled RNA synthesized in parallel.
Publisher
Cold Spring Harbor Laboratory
Subject
General Biochemistry, Genetics and Molecular Biology
Cited by
3 articles.
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