We narrowed to 169,584 results for: addgene

#236288-AAV8

Ready-to-use AAV8 particles produced from pAAV.TBG.PI.FLPo.rBG (#236288). In addition to the viral particles, you will also receive purified pAAV.TBG.PI.FLPo.rBG plasmid DNA. TBG-driven expression of the recombinase FLPo. These AAV preparations are suitable purity for injection into animals.

Melina Fan, Addgene Research Program

Oct. 23, 2025

Academic Institutions and Nonprofits only

#69571-AAV1

Ready-to-use AAV1 particles produced from pAAV-EF1a-C-CreintG (#69571). In addition to the viral particles, you will also receive purified pAAV-EF1a-C-CreintG plasmid DNA. EF1a-driven expression of optimized C-terminal component of Cre recombinase dependent on GFP (Cre-DOG OPT); to be coinjected with pAAV-EF1a-N-CretrcintG (Addgene catalog# 69570) and GFP (or for use with transgenic GFP animals). These AAV preparations are suitable purity for injection into animals.

Connie Cepko

Tang et al Nat Neurosci. 2015 Sep;18(9):1334-41. do

Feb. 19, 2020

Academic Institutions and Nonprofits only

#69570-AAV1

Ready-to-use AAV1 particles produced from pAAV-EF1a-N-CretrcintG (#69570). In addition to the viral particles, you will also receive purified pAAV-EF1a-N-CretrcintG plasmid DNA. EF1a-driven expression of optimized N-terminal component of Cre recombinase dependent on GFP (Cre-DOG OPT); to be coinjected with pAAV-EF1a-C-CreintG (Addgene catalog# 69571) and GFP (or for use with transgenic GFP animals). These AAV preparations are suitable purity for injection into animals.

Connie Cepko

Tang et al Nat Neurosci. 2015 Sep;18(9):1334-41. do

Feb. 19, 2020

Academic Institutions and Nonprofits only

#100798-AAV1

Ready-to-use AAV1 particles produced from pAAV-syn-FLEX-splitTVA-EGFP-tTA (#100798). In addition to the viral particles, you will also receive purified pAAV-syn-FLEX-splitTVA-EGFP-tTA plasmid DNA. Helper virus for monosynaptic tracing with rabies virus; to be coinjected with pAAV-TREtight-mTagBFP2-B19G (Addgene#100799). These AAV preparations are suitable purity for injection into animals.

Ian Wickersham

Liu et al Nature. 2017 Aug 31;548(7669):582-587. d

Dec. 18, 2018

Academic Institutions and Nonprofits only

#100799-AAV1

Ready-to-use AAV1 particles produced from pAAV-TREtight-mTagBFP2-B19G (#100799). In addition to the viral particles, you will also receive purified pAAV-TREtight-mTagBFP2-B19G plasmid DNA. Helper virus for monosynaptic tracing with rabies virus; to be coinjected with pAAV-syn-FLEX-splitTVA-EGFP-tTA (Addgene# 100798). These AAV preparations are suitable purity for injection into animals.

Ian Wickersham

Liu et al Nature. 2017 Aug 31;548(7669):582-587. d

Dec. 18, 2018

Academic Institutions and Nonprofits only

#1000000227

A collection of standardized parts compatible with CIDAR MoClo (Addgene #1000000059) to assemble gene expression constructs in many bacteria across Pseudomonadota.

Eric Young

Sept. 20, 2023

Academic Institutions and Nonprofits only

#1000000161

Plasmids to efficiently build a wide variety of gene expression constructs. Can be used as a stand-alone toolkit or with the CIDAR MoClo Parts Kit (Addgene #1000000059).

Richard Murray

Feb. 7, 2020

Academic Institutions and Nonprofits only

#159446

E. coli BW25113 ΔfrmA, harboring plasmid Addgene plasmid # 129104, was adaptively evolved to grow efficiently on threonine and perform significant biosynthesis while employing methanol-derived carbon

Maciek R. Antoniewicz, Eleftherios Terry Papoutsakis

Har et al Appl Microbiol Biotechnol. 2021 Jan;105(

Aug. 18, 2021

Industry, Academic Institutions, and Nonprofits

#1000000253

Plasmids to quickly and efficiently build a wide variety of gene expression constructs using the EcoFlex-standard MoClo system (Addgene #1000000080).

Mikhail Shapiro

March 11, 2025

Academic Institutions and Nonprofits only

#11794

Lawrence Loeb

Camps et al Proc Natl Acad Sci U S A. 2003 Aug 19. 1

June 20, 2007

Academic Institutions and Nonprofits only

#229395

Escherichia coli DH10B DAP-auxotrophic strain containing an integrated RK2/RP4 mobilization vector to conjugate plasmids with an IncP origin of transfer (modified pTA-Mob 2.0, AddGene Plasmid #149662)

Michael Springer

Soltysiak et al ACS Synth Biol. 2025 Apr 18;14(4):1173-1

March 24, 2025

Academic Institutions and Nonprofits only

#166036

Loopometer recipient strain: lacI- Oid+ control

Keith Shearwin

Hao et al Nucleic Acids Res. 2021 Jan 28. pii: 612

May 26, 2021

Academic Institutions and Nonprofits only

#166037

Loopometer recipient strain: lacI+ Oid- control

Keith Shearwin

Hao et al Nucleic Acids Res. 2021 Jan 28. pii: 612

May 26, 2021

Academic Institutions and Nonprofits only

#166038

Loopometer recipient strain: lacI+ Oid+

Keith Shearwin

Hao et al Nucleic Acids Res. 2021 Jan 28. pii: 612

May 26, 2021

Academic Institutions and Nonprofits only

#37167

Gary Roberts

Aug. 3, 2012

Academic Institutions and Nonprofits only

#197113

E. coli BL21(DE3) derivative for diterpenoid production with genome-integrated yeast MEV pathway, redox enzyme array, and Marionette cluster

Christopher Voigt

Lin et al Nature Catalysis. 6, 1016–1029 (2023). h

June 30, 2023

Academic Institutions and Nonprofits only

#197112

E. coli BL21(DE3) derivative for sesquiterpenoid production with genome-integrated yeast MEV pathway, redox enzyme array, and Marionette cluster

Christopher Voigt

Lin et al Nature Catalysis. 6, 1016–1029 (2023). h

June 30, 2023

Academic Institutions and Nonprofits only

#87359

This is C321.∆A with additional mutations engineered by Kuznetsov et al. to improve doubling time.

George Church

Kuznetsov et al Genome Biol. 2017 May 25;18(1):100. doi:

May 1, 2017

Academic Institutions and Nonprofits only

#37170

Gary Roberts

Aug. 23, 2012

Academic Institutions and Nonprofits only

#37176

Gary Roberts

Aug. 3, 2012

Academic Institutions and Nonprofits only