Cite as: Cold Spring Harb. Protoc.; 2006; doi:10.1101/pdb.prot3222
| 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
Markers for pulsed-field gel electrophorsis can be generated by ligation of linear monomers of bacteriophage
DNA (48.5 kb) into a nested series of concatemers. This procedure yields a series of concatemers that contain up to 20 tandemly arranged copies of bacteriophage DNA.
MATERIALS
1x Ligation buffer with PEG
METHOD
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