Improved LM-PCR Procedure for In Vivo Footprinting Analysis of GC-Rich Promoters
Author:
Affiliation:
1. Institut de Génétíque Moléculaire, UMR 5535 CNRS, Montpellier, France
Publisher
Future Science Ltd
Subject
General Biochemistry, Genetics and Molecular Biology,Biotechnology
Link
https://www.future-science.com/doi/pdf/10.2144/99265bm08
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Ionic liquids promote PCR amplification of DNA;Chemical Communications;2012
2. An improved, real-time PCR assay for the detection of GC-rich and low abundance templates of Mycobacterium tuberculosis;Journal of Microbiological Methods;2006-03
3. The periodic down regulation of Cyclin E gene expression from exit of mitosis to end of G1 is controlled by a deacetylase- and E2F-associated bipartite repressor element;Oncogene;2001-07
4. Dimethyl Sulfoxide as Additive in Ready-to-Use Reaction Mixtures for Real-Time Polymerase Chain Reaction Analysis with SYBR Green I Dye;Analytical Biochemistry;2001-02
5. A CDE/CHR-like element mediates repression of transcription of the mouseRB2 (p130)gene;FEBS Letters;2000-04-05
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