An efficient and economic enhancer mix for PCR
- 1 September 2006
- journal article
- Published by Elsevier BV in Biochemical and Biophysical Research Communications
- Vol. 347 (3), 747-751
- https://doi.org/10.1016/j.bbrc.2006.06.151
Abstract
No abstract availableKeywords
Funding Information
- Max-Planck-Gesellschaft
- Bundesministerium für Bildung und Forschung (01GR0414)
This publication has 13 references indexed in Scilit:
- Present and future of rapid and/or high-throughput methods for nucleic acid testingClinica Chimica Acta; International Journal of Clinical Chemistry, 2006
- Improved PCR Method for Amplification of GC-Rich DNA SequencesMolecular Biotechnology, 2005
- High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5' to 3' exonuclease activity.Genome Research, 1993
- Rapid purification of high-activityTaqDNA polymeraseNucleic Acids Research, 1993
- Intervening sequences in an Archaea DNA polymerase gene.Proceedings of the National Academy of Sciences of the United States of America, 1992
- Purification of Thermus aquaticus DNA polymerase expressed in Escherichia coliAnalytical Biochemistry, 1990
- The Unusual Origin of the Polymerase Chain ReactionScientific American, 1990
- Formamide can dramatically improve the specificity of PCRNucleic Acids Research, 1990
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985