DocumentCode :
2497644
Title :
An Effective Combined-Enhancer for the PCR Amplification of GC-Rich Longer DNA Sequences
Author :
Liu, Fang ; Zhu, Wenze ; Zhang, Zhizhou
Author_Institution :
Teda Bic-X Center for Syst. Bio Technol., Tianjin Univ. of Sci. & Technol., Tianjin, China
fYear :
2009
fDate :
11-13 June 2009
Firstpage :
1
Lastpage :
6
Abstract :
DNA manipulation technology is facing more challenges in the postgenomics era. The amplification of GC-rich longer DNA fragments PCR more difficult than others . through more and more enhancers have been investigated for their potential implications in developing better gene technology. In this study, we reported a beneficial effect of combined-enhancer in enhancing the specificity and total efficiency of GC-rich (GC% ges 65%) longer DNA fragments PCR. Combined-enhancer is a concentration-dependent combination of 5.5 M betaine ,0.5u pfu enzyme, 1.5 mM the mixture of 1,2- propylene glycol and ethylene glycol (the ration of 1,2- propylene glycol and ethylene glycol = 1:1)in 25 muL PCR condition. The combined-enhancer broadly enhanced the quantitative and/or qualitative output of GC-rich (GC% ges 65) longer DNA fragments PCRs.
Keywords :
DNA; biochemistry; genomics; molecular biophysics; 1,2-propylene glycol; DNA manipulation technology; GC rich long DNA sequences; PCR amplification; betaine; combined enhancer; ethylene glycol; pfu enzyme; polymerase chain reaction; specificity enhancement; total efficiency enhancement; Anti-freeze; Biochemistry; Bioinformatics; Blood; DNA; Genomics; Humans; Polymers; Protocols; Sequences;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
Conference_Location :
Beijing
Print_ISBN :
978-1-4244-2901-1
Electronic_ISBN :
978-1-4244-2902-8
Type :
conf
DOI :
10.1109/ICBBE.2009.5162313
Filename :
5162313
Link To Document :
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