We narrowed to 22,785 results for: Ide

#127842

For performing high-throughput cell state-specific synthetic promoter screening

Timothy Lu

Wu et al Nat Commun. 2019 Jun 28;10(1):2880. doi:

Aug. 22, 2020

Academic Institutions and Nonprofits only

#132561

Activation library targeting human SLC proteins.

Giulio Superti-Furga

Rebsamen et al Life Sci Alliance. 2022 Sep 16;5(11):e20

May 18, 2020

Academic Institutions and Nonprofits only

#69763

Used for genome scale lentiviral CRISPR screening. Target sites were chosen in a region close to the translation initiation site.

Haoquan Wu

Ma et al Cell Rep. 2015 Jul 28;12(4):673-83. doi:

Feb. 9, 2016

Academic Institutions and Nonprofits only

#247026

Human genome-wide CRISPR knockout library for the use of S. pyogenes Cas9. Each gene is targeted by 3 constructs.

John Doench, David Root

Drepanos et al bioRxiv 2025.08.26.672375; doi: https://

Oct. 2, 2025

Academic Institutions and Nonprofits only

#75313

Human sgRNA library in backbone lentiGuide-Puro targeting 763 kinase genes and containing 3,052 unique sgRNAs along with 100 non-targeting controls

John Doench, David Root

Doench et al Nat Biotechnol. 2016 Jan 18. doi: 10.103

June 27, 2016

Academic Institutions and Nonprofits only

#75315

Human sgRNA library in backbone lentiCRISPRv2 targeting 763 kinase genes and containing 3,052 unique sgRNAs along with 100 non-targeting controls

John Doench, David Root

Doench et al Nat Biotechnol. 2016 Jan 18. doi: 10.103

June 27, 2016

Academic Institutions and Nonprofits only

#137999

Knockout library that delivers random pairs of optimised gRNAs, reducing screens scale with similar performance to larger libraries.

Leopold Parts

Peets et al bioRxiv 859652

Oct. 15, 2020

Academic Institutions and Nonprofits only

#64750

Library designed for genomic targeting and screening in Drosophila cells. All possible gRNA target sites within the shared exonic regions on either DNA strand of the Drosophila genome were computed.

Ji-Long Liu

Bassett et al J Genet Genomics. 2015 Jun 20;42(6):301-

March 7, 2016

Academic Institutions and Nonprofits only

#243681

For stable recombination of nearly all human GPCRs with unique molecular identifiers.

Jonathan Schlebach

Tedman et al bioRxiv [Preprint]. 2025 Sep 21:2025.09.

Oct. 27, 2025

Academic Institutions and Nonprofits only

#216134

Library of intron-targeting sgRNAs for pooled tagging of proteins with GFP or other protein tags at their endogenous genomic locus using an intron tagging approach.

Stefan Kubicek

Reicher et al Nat Cell Biol. 2024 May;26(5):745-756. d

April 19, 2024

Academic Institutions and Nonprofits only

#216133

Library of intron-targeting sgRNAs for pooled tagging of proteins with GFP or other protein tags at their endogenous genomic locus using an intron tagging approach.

Stefan Kubicek

Reicher et al Nat Cell Biol. 2024 May;26(5):745-756. d

April 19, 2024

Academic Institutions and Nonprofits only

#190744

Targets proximal poly(A) signal sequences in genes identified to be differentially polyadenylated in the mouse B16-F10 melanoma system.

Robert Bradley

Gabel et al Nat Commun. 2024 Feb 1;15(1):959. doi: 1

Feb. 2, 2024

Academic Institutions and Nonprofits only

#197348

To allow for genome-wide genetic modifier screening, the library has a second fixed non-targeting control guide.

Rebecca Voorhees, Jonathan Weissman

Guna et al BMC Genomics. 2023 Oct 30;24(1):651. doi

May 25, 2023

Academic Institutions and Nonprofits only

#197349

To allow for genome-wide genetic modifier screening, the library has a second fixed guide targeting EMC2.

Rebecca Voorhees, Jonathan Weissman

Guna et al BMC Genomics. 2023 Oct 30;24(1):651. doi

May 25, 2023

Academic Institutions and Nonprofits only

#118727

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

David Bikard

Rousset et al PLoS Genet. 2018 Nov 7;14(11):e1007749.

April 1, 2019

Academic Institutions and Nonprofits only

#104052-AAVPHP.V1

Ready-to-use AAV PHP.V1 particles produced from pAAV-CAG-DIO-EYFP (#104052). In addition to the viral particles, you will also receive purified pAAV-CAG-DIO-EYFP plasmid DNA. CAG-driven, Cre-dependent expression of EYFP. These AAV were produced with the PHP.V1 serotype, which permits efficient transduction of brain vascular cells. These AAV preparations are suitable purity for injection into animals.

Viviana Gradinaru

Challis et al Nat Protoc. 2019 Feb;14(2):379-414. doi:

July 24, 2020

Academic Institutions and Nonprofits only