Literature DB >> 19454215

pGreen-S: a clone vector bearing absence of enhanced green fluorescent protein for screening recombinants.

Jinbao Tang1, Shujuan Liang, Jinbao Zhang, Zhiqin Gao, Suhua Zhang.   

Abstract

The bacterial cloning vector, pGreen-S, was constructed by inserting the enhanced green fluorescent protein (EGFP) gene at the XbaI restriction site of pUC18 plasmid. When expressed in Escherichia coli DH5alpha produced colonies that were an absinthe green color under daylight and strongly fluorescent green under longwave ultraviolet light. The pGreen-S vector was used to select for directional insert based on the loss of green fluorescence in recombinant colonies that was caused by the absence of EGFP. The EGFP reporter system differs from the conventional complementation of lacZ, making screening recombinants simpler, less expensive, and more effective.

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Year:  2009        PMID: 19454215     DOI: 10.1016/j.ab.2009.02.007

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  2 in total

1.  Preparation of a bio-immunoreagent between ZZ affibody and enhanced green fluorescent protein for immunofluorescence applications.

Authors:  Hong-Ming Yang; Yong Chen; Zhi-Qin Gao; Jin-Bao Tang
Journal:  World J Microbiol Biotechnol       Date:  2011-05-03       Impact factor: 3.312

2.  White and green screening with circular polymerase extension cloning for easy and reliable cloning.

Authors:  Elizabeth B Speltz; Lynne Regan
Journal:  Protein Sci       Date:  2013-05-08       Impact factor: 6.725

  2 in total

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