Literature DB >> 21601558

Simple cloning strategy using GFPuv gene as positive/negative indicator.

Hiromi Miura1, Hidetoshi Inoko, Ituro Inoue, Masafumi Tanaka, Masahiro Sato, Masato Ohtsuka.   

Abstract

Because construction of expression vectors is the first requisite in the functional analysis of genes, development of simple cloning systems is a major requirement during the postgenomic era. In the current study, we developed cloning vectors for gain- or loss-of-function studies by using the GFPuv gene as a positive/negative indicator of cloning. These vectors allow us to easily detect correct clones and obtain expression vectors from a simple procedure by means of the combined use of the GFPuv gene and a type IIS restriction enzyme.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21601558     DOI: 10.1016/j.ab.2011.04.040

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


  2 in total

1.  Random mutagenesis by error-prone pol plasmid replication in Escherichia coli.

Authors:  David L Alexander; Joshua Lilly; Jaime Hernandez; Jillian Romsdahl; Christopher J Troll; Manel Camps
Journal:  Methods Mol Biol       Date:  2014

2.  Ribosomal binding site switching: an effective strategy for high-throughput cloning constructions.

Authors:  Yangbo Hu; Lipeng Feng; Yunlong Li; Yong Zhang; Pei Lu; Simon Rayner; Shiyun Chen
Journal:  PLoS One       Date:  2012-11-21       Impact factor: 3.240

  2 in total

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