Enzyme Treatment-Free and Ligation-Independent Cloning Using Caged Primers in Polymerase Chain Reactions
A new simple scheme for constructing recombinant vectors that does not require any restriction enzyme, ligase, or any other special enzyme treatment has been developed. By using caged primers in PCR, unnatural sticky-ends of any sequence, which are sufficiently long for ligation-independent cloning...
Main Authors: | Akinori Kuzuya, Keita Tanaka, Hitoshi Katada, Makoto Komiyama |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2011-12-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/17/1/328/ |
Similar Items
-
Replacing UV with Blue Light during DNA Purification Increases the Efficiency of Ligation-Independent Cloning
by: Zeinab Sharafi, et al.
Published: (2019-01-01) -
Restriction-ligation-independent production of a TVCV infectious clone and a TVCV-based gene expression vector
by: Andrea Mirauti, et al.
Published: (2023-09-01) -
Recombinant Expressed Vector pET32a (+) S Constructed by Ligation Independent Cloning
by: Yu Wang, et al.
Published: (2014-10-01) -
A ligation-independent cloning method using nicking DNA endonuclease
by: Jie Yang, et al.
Published: (2010-11-01) -
‘Two in One’ Cloning Vector Applied for Blunt-End and T-A Cloning with One-Step Digestion–Ligation and Screening of Positive Recombinants by Unaided Eyes
by: Xingli Zhang, et al.
Published: (2024-12-01)