Nucleic Acids Research, Vol 27, Issue 3 917-918, Copyright © 1999 by Oxford University Press
M Kenzelmann and K Muhlemann
The efficiency of the original SAGE (Serial Analysis of Gene Expression)
protocol was limited by a small average size of cloned concatemers. We
describe a modification of the technique that overcomes this problem.
Ligation of ditags yields concatemers of various sizes. Small concatemers
may aggregate and migrate with large ones during gel electrophoresis. A
heating step introduced before gel electrophoresis breaks such
contaminating aggregates. This modification yields cloned concatemers with
an average size of 67 tags as compared to 22 tags by the original protocol.
It enhances the length of cloned concatemers substantially and reduces the
costs of SAGE.
ARTICLES
Substantially enhanced cloning efficiency of SAGE (Serial Analysis of Gene Expression) by adding a heating step to the original protocol
Institute of Medical Microbiology, University of Bern, Friedbuhlstrasse 51, 3010 Bern, Switzerland.
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