Sigma-Aldrich
Life Science

Antibodies
Automation
Cancer Research
Cell Culture
Cell Signaling and Neuroscience
Custom Synthesis
Drug Discovery
Epigenetics
Functional Genomics and RNAi
Metabolomics
Molecular Biology
Automated Sequencing
Cloning and Expression
DNA and RNA Purification
Gene Expression Analysis
Molecular Biology Reagents
Nucleic Acid Detection
Nucleic Acid Electrophoresis
PCR
Whole Genome Amplification
New Products
Neuroscience
Nutrition Research
Obesity Research
Peptides and Proteins
Plant Biotechnology
Proteomics and Protein Expr.
Stable Isotopes
Stem Cell Biology
Your Favorite Gene - Search
Life Science Innovations
PathFinder

 Product List for "Selection of Poly(A)+ RNA by Oligo(dT)-Cellulose Chromatography" Protocol

Sigma-Aldrich Research Biotechnology
 

The following Cold Spring Harbor Laboratory Press protocols are brought to you by BioSupplyNet in a partnership with Sigma-Aldrich. A list of products is available to use in each protocol.

View the protocol on BioSupplyNet.com.

Selected Protocol from "Molecular Cloning: A Laboratory Manual", Third Edition, Joseph Sambrook, David W. Russell.

Selection of Poly(A)+ RNA by Oligo(dT)-Cellulose Chromatography

Joseph Sambrook -- Peter Maccallum Cancer Institute and The University of Melbourne, Australia
David W. Russell -- University of Texas Southwestern Medical Center, Dallas

Buy this book, M8265

ABSTRACT
Chromatography on oligo(dT) columns is the preferred method for large-scale purification (>25 mg) of poly(A)+ RNAextracted from mammalian cells. Typically, between 1% and 10% of the RNA applied to the oligo(dT) column is recovered as poly(A)+ RNA. Because the method can be frustratingly slow, it is not recommended for purification of poly(A)+ RNA from multiple samples. For this purpose, batch elution (Protocol 7.4) is the better choice.
IMPORTANT: Prepare all reagents used in this protocol with DEPC-treated H2O.

Products Available for this Protocol

Protocol Material Description Product #  Product Name Add to Cart
2x Column-loading buffer      
40 mM Tris-HCl (pH 7.6) T5941 Trizma® hydrochloride for molecular biology, Biotechnology Performance Certified
1 mM NaCl S3014 Sodium chloride for molecular biology
2 mM EDTA (pH 8.0) E5134 Ethylenediaminetetraacetic acid disodium salt solution for molecular biology
Elution Buffer      
10 mM Tris-HCl (pH 7.6) T5941 Trizma® hydrochloride for molecular biology, Biotechnology Performance Certified
1 mM EDTA (pH 8.0) E5134 Ethylenediaminetetraacetic acid disodium salt solution for molecular biology
0.05% SDS L4390 Sodium dodecyl sulfate for molecular biology
NaCl (5M), Rnase-free S3014 Sodium chloride for molecular biology
Ethanol E7023 Ethanol
NaOH (10 N) 72068 Sodium hydroxide solution, BioChemika Ultra, for molecular biology
Sodium acetate (3 M, pH 5.2) S7899 Sodium acetate buffer solution
Oligo(dt)-cellulose O3131 Oligo(dT)-Cellulose
pH Paper (pH Test Strips) P4786 pH Test strips

Note: As an alternative, the entire protocol could be accomplished with product MRN10 or MRN70, the GenElute™ mRNA Miniprep Kits.

back to top
View all available Cold Spring Harbor Laboratory Press Protocols

Product Association Disclaimer: The Sigma-Aldrich products listed for this specific protocol were selected either to match or to supplement the products listed within the actual protocol. The products/reagents from Sigma-Aldrich have been qualified for usage, but may not have been validated for this specific application. Please refer to the detailed product description on the usage of specific products of interest.