• 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