Cite as: Cold Spring Harb. Protoc.; 2006; doi:10.1101/pdb.prot4048
| Protocol |
This protocol was adapted from Molecular Cloning, 3rd edition, by Joseph Sambrook and David W. Russell. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, USA, 2001
| The first 15% of the full text of this article appears below. |
INTRODUCTION
When many RNA samples are to be processed or when working with small amounts (<50 µg) of total mammalian RNA, the technique of choice is batch chromatography on oligo(dT)-cellulose. The method described in this protocol uses a combination of temperature and ionic strength to maximize binding and recovery of polyadenylated RNA. IMPORTANT: Prepare all reagents used in this protocol with Diethyl pyrocarbonate (DEPC)-treated H2O.
MATERIALS
Ammonium acetate (10 M)
Ice-cold water
RNA absorption/washing buffer
This buffer is TES containing 0.5 M
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