We narrowed to 21,181 results for: ato

#84446-AAV8

Ready-to-use AAV8 particles produced from pAAV-CAG-FLEX-rc [Jaws-KGC-tdTomato-ER2] (#84446). In addition to the viral particles, you will also receive purified pAAV-CAG-FLEX-rc [Jaws-KGC-tdTomato-ER2] plasmid DNA. CAG-driven, Cre-dependent expression of Jaws-KGC-tdTomato-ER2 for optogenetic inhibition. These AAV preparations are suitable purity for injection into animals.

Edward Boyden

Chuong et al Nat Neurosci. 2014 Aug;17(8):1123-9. doi

June 21, 2024

Academic Institutions and Nonprofits only

#51082-AAV1

Ready-to-use AAV1 particles produced from AAV-EF1a-DIO-GCaMP6s-P2A-nls-dTomato (#51082). In addition to the viral particles, you will also receive purified AAV-EF1a-DIO-GCaMP6s-P2A-nls-dTomato plasmid DNA. GCaMP6s calcium sensor and bicistronic, physically separate nuclear localized dTomato expression under the EF1a promoter. These AAV preparations are suitable purity for injection into animals.

Jonathan Ting

Sept. 19, 2017

Academic Institutions and Nonprofits only

#51083-AAVrg

Ready-to-use AAV Retrograde particles produced from AAV-EF1a-DIO-GCaMP6f-P2A-nls-dTomato (#51083). In addition to the viral particles, you will also receive purified AAV-EF1a-DIO-GCaMP6f-P2A-nls-dTomato plasmid DNA. Cre-dependent GCaMP6f calcium sensor and physically separate nuclear tdTomato, under control of the EF1a 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.

Jonathan Ting

June 7, 2017

Academic Institutions and Nonprofits only

#224173-AAV2

Ready-to-use AAV2 particles produced from AiP13738 - pAAV-AiE0743m_3xC2-minBG-tdTomato-WPRE3-BGHpA (Alias: CN3738) (#224173). In addition to the viral particles, you will also receive purified AiP13738 - pAAV-AiE0743m_3xC2-minBG-tdTomato-WPRE3-BGHpA (Alias: CN3738) plasmid DNA. minBG-driven expression of tdTomato in striatal cholinergic neurons. These AAV preparations are suitable purity for injection into animals.

Allen Institute for Brain Science, Jonathan Ting

Hunker et al Neuron. 2025 May 21;113(10):1507-1524.e1

Nov. 14, 2025

Academic Institutions and Nonprofits only

#232069

Knockout library for use in CRASP-Seq experiments. Provides a flexible platform for studying splicing regulation.

Thomas Gonatopoulos-Pournatzis

Behera et al Mol Cell. 2026 Jan 8;86(1):41-59.e15. do

Oct. 28, 2025

Academic Institutions and Nonprofits only

#232068

The CRASP-Seq backbone is designed to accommodate the cloning of diverse gRNA libraries. It includes a cell barcode (CBC), which enhances its functionality by enabling library preparation.

Thomas Gonatopoulos-Pournatzis

Behera et al Mol Cell. 2026 Jan 8;86(1):41-59.e15. do

Oct. 28, 2025

Academic Institutions and Nonprofits only

#232070

Tiling library to conduct CRASP-Seq experiments combined with high-throughput base editing for precise and scalable investigations into protein regions that affect splicing regulation.

Thomas Gonatopoulos-Pournatzis

Behera et al Mol Cell. 2026 Jan 8;86(1):41-59.e15. do

Oct. 28, 2025

Academic Institutions and Nonprofits only

#1000000213

A set of plasmids containing barcoded self-reporting transposons used for 'calling card' experiments to identify transcription factor binding sites and changes in gene expression.

Rob Mitra

Feb. 16, 2023

Academic Institutions and Nonprofits only

#237473

Enables high-throughput identification of frame-preserving exons that influence transcriptional phenotypes, building on the CHyMErA system (Nature Biotechnology, 2020; PMID: 32249828).

Thomas Gonatopoulos-Pournatzis

Kumari et al Nat Commun. 2026 Feb 3;17(1):1218. doi:

Oct. 28, 2025

Academic Institutions and Nonprofits only

#155200

Hybrid guide RNA library targeting human alternative cassette exons for deletion and disruption

Benjamin Blencowe, Jason Moffat

Gonatopoulos-Pournatzis et al Nat Biotechnol. 2020 May;38(5):638-648.

Sept. 2, 2020

Academic Institutions and Nonprofits only

#155199

Hybrid guide RNA library targetings human paralog pairs and other protein-coding genes.

Benjamin Blencowe, Jason Moffat

Gonatopoulos-Pournatzis et al Nat Biotechnol. 2020 May;38(5):638-648.

Sept. 2, 2020

Academic Institutions and Nonprofits only

#209734

CHyMErA Cas12a Nuclease Optimization hgRNA Libraries allows assessment and comparison of the efficacy of different LbCas12a nucleases in the context of the Cas9-Cas12a CHyMErA system.

Thomas Gonatopoulos-Pournatzis

Xiao et al Mol Cell. 2024 Jul 11;84(13):2553-2572.e

June 20, 2024

Academic Institutions and Nonprofits only

#209735

CHyMErA Cas12a Nuclease Optimization hgRNA Libraries allows assessment and comparison of the efficacy of different AsCas12a nucleases in the context of the Cas9-Cas12a CHyMErA system.

Thomas Gonatopoulos-Pournatzis

Xiao et al Mol Cell. 2024 Jul 11;84(13):2553-2572.e

June 20, 2024

Academic Institutions and Nonprofits only

#1000000060

A plasmid toolbox used to construct vectors for constitutive or inducible gene expression, knockdown, deletion or editing.

Ian Frew

June 16, 2015

Academic Institutions and Nonprofits only

#209736

CHyMErA Exon Deletion hgRNA Library allows identification of frame-preserving exons that affect cell fitness in human cells using the CHyMErA screening platform.

Thomas Gonatopoulos-Pournatzis

Xiao et al Mol Cell. 2024 Jul 11;84(13):2553-2572.e

June 20, 2024

Academic Institutions and Nonprofits only

#1000000259

Plasmids and parts for modular assembly of single and multi-gene plasmids for any Xanthobacter or Roseixanthobacter strain.

Michael Springer

June 16, 2025

Academic Institutions and Nonprofits only

#170511

Genome-wide knockout library. It is identical to the Brie library #73633, replacing Puromycin resistance with mCherry.

Pavel Tolar

Newman et al bioRxiv 2021.03.02.433398

Sept. 9, 2021

Academic Institutions and Nonprofits only