@article{MAKHILLJAVA201211203816,
    title = {Characterization of &#946;-Actin Promoter of <I>Leuciscus merzbacheri</I>},
    journal = {Journal of Animal and Veterinary Advances},
    volume = {11},
    number = {20},
    pages = {3849-3854},
    year = {2012},
    issn = {1680-5593},
    doi = {javaa.2012.3849.3854},
    url = {https://makhillpublications.co/view-article.php?issn=1680-5593&doi=javaa.2012.3849.3854},
    author = {Shiwei,Wenge,Chuangfu,Yuanzhi,Yan,Xudong and},
    keywords = {Leuciscus merzbacheri,promoter analysis,B-actin gene,green fluorescent protein,China},
    abstract = {<I>Leuciscus merzbacheri</I> is a unique vulnerable indigenous 
  fish which is only distributed in the Junggar Basin, Xinjiang. In this study, 
  researchers cloned two <I>L. merzbacheri</I> &#946;-actin promoter fragments 
  of different length: SZ11 and SZ21 and analyzed their structural features. The 
  mammalian expression vector pEGFP-N1 was used to construct eukaryotic expression 
  vectors &#946;1 pEGFP-N1-AFP III and &#946;2 pEGFP-N1-AFP III in which fish 
  type III antifreeze protein gene was used as the structural gene. The results 
  showed that the cloned two fragments of &#946;-actin promoters had the ability 
  to drive the expression of the green fluorescent protein gene in BHK-21 cells. 
  These data suggest that the vectors researchers constructed based on &#946;-actin 
  promoter could be exploited as all fish recombinant eukaryotic expression vector.}
    }