Please cite as: CSH Protocols; 2006; doi:10.1101/pdb.prot3514
| 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
Mammalian DNA prepared from blood or tissues as described in this protocol is 20-50 kb in size and suitable for use as a template in PCRs. The yields of DNA vary between 0.5 and 3.0 µg/mg tissue or 5 and 15 µg per 300 µl of whole blood.
MATERIALS
DNase-free RNase (4 mg/ml)
Ethanol
Optional, please see Step 5.
Isopropanol
Mammalian tissue
Potassium acetate (5 M)
Proteinase K (20 mg/ml)
Use of a genomic grade proteinase K that has been shown to be free of DNase and RNase activity.
Rapid
METHOD
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