منابع مشابه
Preparative-scale purification of RNA using an efficient method which combines gel electrophoresis and column chromatography.
Here we describe a reliable method for purifying large amounts of RNA of any sequence and length with comparable efficiency and resolution of gel electrophoresis and with capacity approaching that of column chromatography. The RNA mixture of interest is separated on a cylindrical denaturing polyacrylamide gel, eluted by a peristaltic pump, detected by a UV-vis detector, and collected by a fract...
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RNA-based applications requiring high-quality, non-degraded RNA are a foundational element of many research studies. As such, it is paramount that the integrity of experimental RNA is validated prior to cDNA synthesis or other downstream applications. In the absence of expensive equipment such as microfluidic electrophoretic devices, and as an alternative to the costly and time-consuming standa...
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Caulobacter crescentus RNA polymerase holoenzyme and core enzyme have been separated by chromatography on denatured DNA-cellulose and purified by phosphocellulose chromatography. In order to assess the functional role of the putative C. crescentus CT subunit, the enzymes were compared to Escherichia coli holoenzyme and core RNA polymerases, and the transcription of various DNA templates by C. c...
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Preparative polyacrylamide gel electrophoresis has been used to purify the enterotoxin of Clostridium perfringens from Sephadex G-100 extracts. Purified toxin of high specific activity was eluted in 1 to 3 h, depending upon the length of the acrylamide gel used. Recovery of biological activity with this technique ranged from 80 to 90%. The purity and physical characteristics of the toxin were s...
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ژورنال
عنوان ژورنال: Cold Spring Harbor Protocols
سال: 2013
ISSN: 1559-6095
DOI: 10.1101/pdb.prot072942