Development of a dual-expression vector facilitated with selection-free PCR recombination cloning strategy-Reference-Cited by-同舟云学术

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Development of a dual-expression vector facilitated with selection-free PCR recombination cloning strategy

Published:2017-05-16 Issue:1 Volume:7 Page:
ISSN:2191-0855
Container-title:AMB Express
language:en
Short-container-title:AMB Expr

Author:

Cao Liting,Zhou Yancheng,Huang Lin,Dong Shiqi,Ma Yue

Funder

Natural Science Foundation of Chongqing, China

Publisher

Springer Science and Business Media LLC

Subject

Applied Microbiology and Biotechnology,Biophysics

Link

http://link.springer.com/content/pdf/10.1186/s13568-017-0386-1.pdf

Reference22 articles.

1. Aslanidis C, Dejong PJ (1990) Ligation-independent cloning of PCR products (Lic-PCR). Nucleic Acids Res 18:6069–6074

2. Bryksin A, Matsumura I (2010) Overlap extension PCR cloning: a simple and reliable way to create recombinant plasmids. Biotechniques 48:463–465

3. Cheo DL, Titus SA, Byrd DR, Hartley JL, Temple GF, Brasch MA (2004) Concerted assembly and cloning of multiple DNA segments using in vitro site-specific recombination: functional analysis of multi-segment expression clones. Genome Res 14:2111–2120

4. Ent FVD, Löwe J (2006) RF cloning: a restriction-free method for inserting target genes into plasmids. J Biochem Biophys Methods 67(1):67–74

5. Henrich B, Lubitz W, Plapp R (1982) Lysis of Escherichia coli by induction of cloned ΦX174 genes. Mol Gen Genet 185(3):493–497

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