We narrowed to 42,257 results for: LAT

#135635-PHPeB

Ready-to-use AAV PHP.eB particles produced from pAAV-S5E2-Gq-P2A-dTomato (#135635). In addition to the viral particles, you will also receive purified pAAV-S5E2-Gq-P2A-dTomato plasmid DNA. Expression of Gq-DREADD and dTomato (physically separate) under the control of the E2 regulatory element. These AAV were produced with the PHPeB serotype, which permits efficient transduction of the central nervous system. These AAV preparations are suitable purity for injection into animals.

Jordane Dimidschstein

Vormstein-Schneider et al Nat Neurosci. 2020 Dec;23(12):1629-1636.

Aug. 27, 2021

Academic Institutions and Nonprofits only

#202199-AAV1

Ready-to-use AAV1 particles produced from pAAV_hSyn-SIO-stChrimsonR-EGFP-P2A-PdCO-miniWPRE (#202199). In addition to the viral particles, you will also receive purified pAAV_hSyn-SIO-stChrimsonR-EGFP-P2A-PdCO-miniWPRE plasmid DNA. Synapsin-driven, Cre-dependent expression of bicistronically soma-targeted ChrimsonR in frame with EGFP and the optimized opsin PdCO. These AAV preparations are suitable purity for injection into animals.

Ofer Yizhar

Wietek et al Nat Methods. 2024 May 29. doi: 10.1038/s

April 10, 2024

Academic Institutions and Nonprofits only

#202199-AAV5

Ready-to-use AAV5 particles produced from pAAV_hSyn-SIO-stChrimsonR-EGFP-P2A-PdCO-miniWPRE (#202199). In addition to the viral particles, you will also receive purified pAAV_hSyn-SIO-stChrimsonR-EGFP-P2A-PdCO-miniWPRE plasmid DNA. Synapsin-driven, Cre-dependent expression of bicistronically soma-targeted ChrimsonR in frame with EGFP and the optimized opsin PdCO. These AAV preparations are suitable purity for injection into animals.

Ofer Yizhar

Wietek et al Nat Methods. 2024 May 29. doi: 10.1038/s

April 10, 2024

Academic Institutions and Nonprofits only

#105321-AAV1

Ready-to-use AAV1 particles produced from pGP-AAV-syn-jGCaMP7c variant 1513-WPRE (#105321). In addition to the viral particles, you will also receive purified pGP-AAV-syn-jGCaMP7c variant 1513-WPRE plasmid DNA. Synapsin-driven jGCaMP7c expression. jGCaMP7c exhibits high contrast between peak fluorescence and resting fluorescence. It is useful for activity imaging of large populations of densely-labeled neurons because background fluorescence from inactive neurons is reduced. These AAV preparations are suitable purity for injection into animals.

Douglas Kim, GENIE Project

Dana et al Nat Methods. 2019 Jul;16(7):649-657. doi

July 12, 2019

Academic Institutions and Nonprofits only

#135633-PHPeB

Ready-to-use AAV PHP.eB particles produced from pAAV-S5E2-C1V1-eYFP (#135633). In addition to the viral particles, you will also receive purified pAAV-S5E2-C1V1-eYFP plasmid DNA. Expression of red-shifted opsin C1V1 fused to EYFP under the control of the E2 regulatory element. These AAV were produced with the PHPeB serotype, which permits efficient transduction of the central nervous system. These AAV preparations are suitable purity for injection into animals.

Jordane Dimidschstein

Vormstein-Schneider et al Nat Neurosci. 2020 Dec;23(12):1629-1636.

Aug. 27, 2021

Academic Institutions and Nonprofits only

#1000000164

Use the Core Optogenetic Vector Collection (OVC) to rapidly generate custom-made optogenetic tools in configurations ABC, BAC, or ACB to regulate protein-protein interactions.

Harald Janovjak

Oct. 9, 2020

Academic Institutions and Nonprofits only

#1000000242

Plasmids for inducible, linkage-specific polyubiquitylation of a protein of interest for in vitro experiments.

Helle Ulrich

May 31, 2024

Academic Institutions and Nonprofits only

#1000000037

Collection of precisely quantitated bacterial transcription and translation initiation elements for controlled and reliable expression in E. coli.

Drew Endy

Dec. 12, 2013

Academic Institutions and Nonprofits only

#62843

amplified library of Salpingoeca rosetta

Nicole King

Fairclough et al Genome Biol. 2013 Feb 18;14(2):R15. doi:

June 16, 2015

Academic Institutions and Nonprofits only

#62844

amplified library of Salpingoeca rosetta from a colony rich culture which included the colony inducing bacteria Algoriphagus machipongonensis

Nicole King

Fairclough et al Genome Biol. 2013 Feb 18;14(2):R15. doi:

June 16, 2015

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

#1000000133

A flexible modular system for advanced strain engineering in Pichia pastoris to accomplish pathway expression, protein production, or other DNA integration applications.

Brigitte Gasser

Feb. 20, 2018

Academic Institutions and Nonprofits only

#1000000255

Regulate gene expression by combining gRNA constructs targeting natural promoters and insertion of synthetic promoters in Yarrowia lipolytica.

Irina Borodina

April 28, 2025

Academic Institutions and Nonprofits only

#1000000244

Plasmids for inducible, linkage-specific polyubiquitylation of a protein of interest in human cells.

Helle Ulrich

May 31, 2024

Academic Institutions and Nonprofits only

#1000000272

Standardized DNA parts and vectors for genetic engineering of the plant synthetic biology model Marchantia polymorpha and other related plant species.

Jim Haseloff

Feb. 6, 2026

Industry, Academic Institutions, and Nonprofits

#217744

Targets 56 transcription factors in Yarrowia lipolytica, enabling the knockout or modulation of expression levels for these factors.

Irina Borodina

May 20, 2025

Academic Institutions and Nonprofits only

#1000000197

Lentiviral plasmids with unique protein barcodes and gRNA cloning sites for CRISPR screens and tracking cell populations. Barcodes are linked to a nuclear-localizing mCherry fluorescent reporter. Part of the Pro-Code Vector Kits.

Brian Brown

Nov. 3, 2022

Academic Institutions and Nonprofits only

#1000000065

Plasmids consisting of open reading frames cloned into the pCellFree vector, which enables protein expression in any in vitro translation system.

Kirill Alexandrov

Nov. 6, 2015

Academic Institutions and Nonprofits only

#125753

Knockout library targeting a set of human interferon-stimulated genes (ISGs).

Michael Emerman, Molly OhAinle

Roesch et al Retrovirology. 2018 Mar 20;15(1):26. doi

May 7, 2020

Academic Institutions and Nonprofits only

#1000000177

Lentiviral plasmids with unique protein barcodes and gRNA cloning sites for CRISPR screens and tracking cell populations. Part of the Pro-Code Vector Kits.

Brian Brown

Sept. 3, 2021

Academic Institutions and Nonprofits only