We narrowed to 40,797 results for: LAT

#50915

Tet-regulatable dCas9 lentiviral expression vector

Rene Maehr, Scot Wolfe

Kearns et al Development. 2014 Jan;141(1):219-23. doi

Feb. 11, 2014

Academic Institutions and Nonprofits only

#229040

Light inducible three-node circuit that can generate ring patterns in a growing bacterial colony upon blue light pulses. Heterologous expression of dCas9, Csy4, and VVD-AraC are necessary.

Yolanda Schaerli

Hollo et al Mol Syst Biol. 2025 Sep 29. doi: 10.1038

Sept. 23, 2025

Academic Institutions and Nonprofits only

#121183

N-terminal tagging

Masato Kanemaki

Yesbolatova et al Methods. 2019 Apr 23. pii: S1046-2023(18

Feb. 13, 2019

Academic Institutions and Nonprofits only

#128407

Conditionally express both AsCas12a and CRISPR arrays on single transcripts

Randall Platt

Campa et al Nat Methods. 2019 Aug 12. pii: 10.1038/s

Nov. 1, 2019

Academic Institutions and Nonprofits only

#203769

For production of template RNA for use in PRINT, GFP under SV40 promoter

Kathleen Collins

Zhang et al Nat Biotechnol. 2024 Feb 20. doi: 10.103

Feb. 27, 2024

Academic Institutions and Nonprofits only

#11586

Cre-regulated lentiviral shRNA vector. Cre addition causes the puromycin gene to be recombined out of the construct, activating shRNA expression.

Tyler Jacks

Ventura et al Proc Natl Acad Sci U S A. 2004 Jul 13. 1

July 19, 2006

Academic Institutions and Nonprofits only

#24312

Roel Nusse

Fuerer et al PLoS One. 2010 . 5(2):e9370.

April 5, 2010

Academic Institutions and Nonprofits only

#21814

David Ron

Harding et al Nature. 1999 Jan 21. 397(6716):271-4.

March 29, 2010

Academic Institutions and Nonprofits only

#128132

Express both AsCas12a fused to [Repr] repressor domain and CRISPR arrays on a single transcript

Randall Platt

Campa et al Nat Methods. 2019 Aug 12. pii: 10.1038/s

Oct. 1, 2019

Academic Institutions and Nonprofits only