We narrowed to 168,206 results for: Gene

#102261

ompA, ompC double knockout strain for overproduction of outer membrane proteins

Jack Leo

Meuskens et al Front Cell Infect Microbiol. 2017 Nov 7;

Nov. 10, 2017

Academic Institutions and Nonprofits only

#52696

MG1655 with Lac Operon removed from native locus and re-integrated at the attTn7 locus

Tanja Kortemme

Eames et al Science. 2012 May 18;336(6083):911-5. do

Feb. 2, 2015

Academic Institutions and Nonprofits only

#102262

ompA, ompF double knockout strain for overproduction of outer membrane proteins

Jack Leo

Meuskens et al Front Cell Infect Microbiol. 2017 Nov 7;

Nov. 10, 2017

Academic Institutions and Nonprofits only

#102267

ompA, lamB, ompF triple knockout strain for overproduction of outer membrane proteins

Jack Leo

Meuskens et al Front Cell Infect Microbiol. 2017 Nov 7;

Nov. 10, 2017

Academic Institutions and Nonprofits only

#102264

lamB, ompF double knockout strain for overproduction of outer membrane proteins

Jack Leo

Meuskens et al Front Cell Infect Microbiol. 2017 Nov 7;

Nov. 10, 2017

Academic Institutions and Nonprofits only

#102260

ompA, lamB double knockout strain for overproduction of outer membrane proteins

Jack Leo

Meuskens et al Front Cell Infect Microbiol. 2017 Nov 7;

Nov. 10, 2017

Academic Institutions and Nonprofits only

#72340

Bacterial strain: E. coli BW25113 ΔlacI ΔaraC ΔsdiA Ptrc*-cinR Ptrc*-rhlR

Matthew Bennett

Chen et al Science. 2015 Aug 28;349(6251):986-9. do

March 10, 2016

Academic Institutions and Nonprofits only

#92352

Focused gRNA library that targets synthetic lethal candidate and control genes with oncogenic Ras.

Eric Lander, David Sabatini

Wang et al Cell. 2017 Feb 1. pii: S0092-8674(17)300

June 7, 2017

Academic Institutions and Nonprofits only

#115924

Expression of dCas9 gene under the control of a Ptet promoter in the E. coli chromosome

David Bikard

Cui et al Nat Commun. 2018 May 15;9(1):1912. doi:

March 26, 2019

Academic Institutions and Nonprofits only

#1000000211

A collection of Multisite Gateway Entry clone plasmids which can be used in a combinatorial fashion to generate large numbers of tagged expression clones for protein expression in a variety of systems

Dominic Esposito

Dec. 22, 2022

Academic Institutions and Nonprofits only