We narrowed to 27,367 results for: STI;

#180310

E. coli MG1655 strain with knockout of endogenous Type I-E CRISPR Cas system

James Chappell

Villegas Kcam et al ACS Synth Biol. 2022 Jan 25. doi: 10.102

May 2, 2022

Academic Institutions and Nonprofits only

#59170-AAV5

Ready-to-use AAV5 particles produced from pAAV-Syn-Chronos-GFP (#59170). In addition to the viral particles, you will also receive purified pAAV-Syn-Chronos-GFP plasmid DNA. Syn-driven Chronos-GFP expression for optogenetic neural activation. These AAV preparations are suitable purity for injection into animals.

Edward Boyden

Klapoetke et al Nat Methods. 2014 Mar;11(3):338-46. doi:

July 21, 2017

Academic Institutions and Nonprofits only

#59170-AAV1

Ready-to-use AAV1 particles produced from pAAV-Syn-Chronos-GFP (#59170). In addition to the viral particles, you will also receive purified pAAV-Syn-Chronos-GFP plasmid DNA. Syn-driven Chronos-GFP expression for optogenetic neural activation. These AAV preparations are suitable purity for injection into animals.

Edward Boyden

Klapoetke et al Nat Methods. 2014 Mar;11(3):338-46. doi:

Feb. 7, 2018

Academic Institutions and Nonprofits only

#62726-AAV8

Ready-to-use AAV8 particles produced from pAAV-Syn-Chronos-tdTomato (#62726). In addition to the viral particles, you will also receive purified pAAV-Syn-Chronos-tdTomato plasmid DNA. Syn-driven Chronos-tdTomato expression for optogenetic neuronal activation. These AAV preparations are suitable purity for injection into animals.

Edward Boyden

Klapoetke et al Nat Methods. 2014 Mar;11(3):338-46. doi:

Feb. 7, 2018

Academic Institutions and Nonprofits only

#59170-AAVrg

Ready-to-use AAV Retrograde particles produced from pAAV-Syn-Chronos-GFP (#59170). In addition to the viral particles, you will also receive purified pAAV-Syn-Chronos-GFP plasmid DNA. Chronos-GFP under the control of the Synapsin promoter. These AAV were produced with a retrograde serotype, which permits retrograde access to projection neurons. These AAV preparations are suitable purity for injection into animals.

Edward Boyden

Klapoetke et al Nat Methods. 2014 Mar;11(3):338-46. doi:

Oct. 3, 2017

Academic Institutions and Nonprofits only

#125258

Derivative of MG1655 used for the screening of clones able to survive the bad seed toxicity of dCas9, while still efficiently silencing the expression of mcherry

David Bikard

Depardieu et al Methods. 2019 Aug 1. pii: S1046-2023(18)

Aug. 23, 2019

Academic Institutions and Nonprofits only

#141407

LacI-deficient E. coli host bacterium that produces β-galactosidase constitutively

Antal Kiss

Szentes et al Nucleic Acids Res. 2020 Mar 18;48(5):e28

Aug. 4, 2020

Academic Institutions and Nonprofits only

#163489-AAV1

Ready-to-use AAV1 particles produced from AiP1051-pAAV-Synapsin promoter-oNigri-WPRE-hGHpA (#163489). In addition to the viral particles, you will also receive purified AiP1051-pAAV-Synapsin promoter-oNigri-WPRE-hGHpA plasmid DNA. Syn-driven expression of codon-optimized Nigri recombinase. These AAV preparations are suitable purity for injection into animals.

Tanya Daigle, Allen Institute for Brain Science

Aug. 6, 2025

Academic Institutions and Nonprofits only

#52962-LV

Ready-to-use Lentiviral Prep particles produced from lentiCas9-Blast (#52962). In addition to the viral particles, you will also receive purified lentiCas9-Blast plasmid DNA. Lentiviral particles carrying Cas9 and blasticidin resistance. This virus is used to make stable cell lines expressing Cas9.

Feng Zhang

Sanjana et al Nat Methods. 2014 Aug;11(8):783-4. doi:

July 14, 2016

Academic Institutions and Nonprofits only

#1000000155

pMVP and pMAGIC are cloning systems for adenoviral, lentiviral, expression, PiggyBac transposon, and Sleeping Beauty transposon vectors for transgene or RNAi delivery and dCas9-based engineering.

Christopher Newgard

Sept. 6, 2019

Academic Institutions and Nonprofits only

#102804

BL21(DE3)-based E. coli amino acid auxotrophic host strain used for selective isotope labeling. thrC ilvA genes deleted.

Robert Gennis, Toshio Iwasaki

Iwasaki et al J Biochem. 2021 Apr 29;169(4):387-394. d

Nov. 8, 2017

Academic Institutions and Nonprofits only

#102801

BL21(DE3)-based E. coli amino acid auxotrophic host strain used for selective isotope labeling. aspC tyrB ilvE genes deleted.

Robert Gennis, Toshio Iwasaki

Iwasaki et al J Biochem. 2021 Apr 29;169(4):387-394. d

Nov. 8, 2017

Academic Institutions and Nonprofits only

#102802

BL21(DE3)-based E. coli amino acid auxotrophic host strain used for selective isotope labeling. aspC tyrB ilvE avtA genes deleted.

Robert Gennis, Toshio Iwasaki

Iwasaki et al J Biochem. 2021 Apr 29;169(4):387-394. d

Nov. 8, 2017

Academic Institutions and Nonprofits only

#102799

BL21(DE3)-based E. coli amino acid auxotrophic host strain used for selective isotope labeling. aspC tyrB trpA trpB glyA serB genes deleted.

Robert Gennis, Toshio Iwasaki

Iwasaki et al J Biochem. 2021 Apr 29;169(4):387-394. d

Nov. 8, 2017

Academic Institutions and Nonprofits only

#102800

BL21(DE3)-based E. coli amino acid auxotrophic host strain used for selective isotope labeling. aspC tyrB trpA trpB glyA serB cysE genes deleted.

Robert Gennis, Toshio Iwasaki

Iwasaki et al J Biochem. 2021 Apr 29;169(4):387-394. d

Nov. 8, 2017

Academic Institutions and Nonprofits only

#102803

BL21(DE3)-based E. coli amino acid auxotrophic host strain used for selective isotope labeling. aspC tyrB ilvE avtA yfbQ(alaA) yfdZ(alaC) genes deleted. (yfbQ also called alaA; yfdZ also called alaC)

Robert Gennis, Toshio Iwasaki

Iwasaki et al J Biochem. 2021 Apr 29;169(4):387-394. d

Nov. 8, 2017

Academic Institutions and Nonprofits only

#1000000030

Contains modified pFUS array vectors and destination vectors that are designed for use with the Golden Gate TALEN and TAL Effector Kit.

Takashi Yamamoto

March 28, 2013

Academic Institutions and Nonprofits only

#229137

Donor vector library to introduce TP53 mutations into the endogenous gene locus at exon 5 of human cells via CRISPR-HDR.

Thorsten Stiewe

Funk et al Nat Genet. 2025 Jan;57(1):140-153. doi:

Feb. 24, 2025

Industry, Academic Institutions, and Nonprofits

#229138

Donor vector library to introduce TP53 mutations into the endogenous gene locus at exon 6 of human cells via CRISPR-HDR.

Thorsten Stiewe

Funk et al Nat Genet. 2025 Jan;57(1):140-153. doi:

Feb. 24, 2025

Industry, Academic Institutions, and Nonprofits