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Article
Rapid Communication: MspI Restriction Fragment Length Polymorphism at the Swine Myogenin Locus
Journal of Animal Science
  • C. W. Ernst, Iowa State University
  • D. A. Vaske, Iowa State University
  • R. G. Larson, Iowa State University
  • Max F. Rothschild, Iowa State University
Document Type
Article
Publication Version
Published Version
Publication Date
1-1-1993
DOI
/1993.71123479x
Abstract

Source and Description of Probe. A 1,486-bp rat cDNA clone for myogenin (MYOG) was excised from the EcoRI site of the plasmid, pBluescrybe M13- (Wright et al., 1989). Method of Detection. DNA was isolated from whole blood and digested with MspI. Fragments were then separated by agarose gel electrophoresis and transferred to charged nylon membranes. Hybridizations were at 65°C for 16 to 20 h (.5 M NaCl, .05 M Naphosphate buffer, pH 6.5, 5x Denhardt's reagent, 10% dextran sulfate, .5% SDS, 100 pg/mL sonicated, denatured salmon sperm DNA). Final washes were at 55 to 60°C in .7x SSC, 5% SDS for 15 to 20 min.

Comments

This is an article from Journal of Animal Science 71 (1993): 3479, doi:/1993.71123479x. Posted with permission.

Copyright Owner
American Society of Animal Science
Language
en
File Format
application/pdf
Citation Information
C. W. Ernst, D. A. Vaske, R. G. Larson and Max F. Rothschild. "Rapid Communication: MspI Restriction Fragment Length Polymorphism at the Swine Myogenin Locus" Journal of Animal Science Vol. 71 Iss. 12 (1993) p. 3479 - 3479
Available at: http://works.bepress.com/max-rothschild/103/