We narrowed to 45,013 results for: ina

#199776-PHPeB

Ready-to-use AAV PHP.eB particles produced from AiP13779 - pAAV-AiE0779m_3xC2-minBG-iCre(R297T)-BGHpA (Alias: CN3779) (#199776). In addition to the viral particles, you will also receive purified AiP13779 - pAAV-AiE0779m_3xC2-minBG-iCre(R297T)-BGHpA (Alias: CN3779) plasmid DNA. Cre recombinase expression in striatal direct pathway medium spiny neurons (D1-MSNs). 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.

Allen Institute for Brain Science, Jonathan Ting

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

July 15, 2024

Academic Institutions and Nonprofits only

#230681-AAV5

Ready-to-use AAV5 particles produced from AiP1636 - pAAV-AiE2116m-minBG-iCre-WPRE-BGHpA (#230681). In addition to the viral particles, you will also receive purified AiP1636 - pAAV-AiE2116m-minBG-iCre-WPRE-BGHpA plasmid DNA. minBG-driven expression of iCre recombinase in specific populations of brain cells. These AAV preparations are suitable purity for injection into animals.

Allen Institute for Brain Science, Bosiljka Tasic

Ben-Simon et al Cell. 2025 May 16:S0092-8674(25)00513-6.

Aug. 6, 2025

Academic Institutions and Nonprofits only

#199775-PHPeB

Ready-to-use AAV PHP.eB particles produced from AiP13778 - pAAV-AiE0450h-minBG-iCre(R297T)-BGHpA (Alias: CN3778) (#199775). In addition to the viral particles, you will also receive purified AiP13778 - pAAV-AiE0450h-minBG-iCre(R297T)-BGHpA (Alias: CN3778) plasmid DNA. Cre recombinase expression in striatal medium spiny neurons. 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.

Allen Institute for Brain Science, Jonathan Ting

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

July 15, 2024

Academic Institutions and Nonprofits only

#111706

Encodes 14-3-3σ and human phosphopeptides fused to split mCherry for Hi-P

Jesse Rinehart

Barber et al Nat Biotechnol. 2018 Aug;36(7):638-644.

Dec. 1, 2022

Academic Institutions and Nonprofits only

#111705

Encodes 14-3-3β and human phosphopeptides fused to split mCherry for Hi-P

Jesse Rinehart

Barber et al Nat Biotechnol. 2018 Aug;36(7):638-644.

Dec. 1, 2022

Academic Institutions and Nonprofits only

#111704

Encodes GST-fused human phosphopeptides

Jesse Rinehart

Barber et al Nat Biotechnol. 2018 Aug;36(7):638-644.

Dec. 1, 2022

Academic Institutions and Nonprofits only

#172650

Set C contains best-ranked guides 1 and 4.

John Doench, David Root

DeWeirdt et al Nat Biotechnol. 2020 Jul 13. pii: 10.103

Nov. 10, 2021

Academic Institutions and Nonprofits only

#172651

Set D contains best-ranked guides 2 and 3.

John Doench, David Root

DeWeirdt et al Nat Biotechnol. 2020 Jul 13. pii: 10.103

Nov. 10, 2021

Academic Institutions and Nonprofits only

#111708

Encodes NEDD4-2 WW2 domain and human phosphopeptides fused to split mCherry for Hi-P

Jesse Rinehart

Barber et al Nat Biotechnol. 2018 Aug;36(7):638-644.

Dec. 1, 2022

Academic Institutions and Nonprofits only

#111707

Encodes NEDD4 WW2 domain and human phosphopeptides fused to split mCherry for Hi-P

Jesse Rinehart

Barber et al Nat Biotechnol. 2018 Aug;36(7):638-644.

Dec. 1, 2022

Academic Institutions and Nonprofits only

#79153

Library of protospacer flanking sites (PFS) inserted at the 5' end of the β-lactamase gene for screening PFS preference for Cas13a/C2c2.

Feng Zhang

Abudayyeh et al Science. 2016 Jun 2. pii: aaf5573.

Oct. 26, 2017

Academic Institutions and Nonprofits only

#123361

CRISPR-Cpf1/Cas12a double knockout library. Targets 26 genes, chosen from analysis of human metastasis cohorts. It can be used to interrogate the genetic interactions driving metastasis.

Sidi Chen

Chow et al Nat Methods. 2019 May;16(5):405-408. doi

June 10, 2019

Academic Institutions and Nonprofits only

#199601

pRep-Cap SSM library enables VP1, VP2, and VP3 expression under the control of the endogenous p40 promoter

George Church

Ogden et al Science. 2019 Nov 29;366(6469):1139-1143

June 13, 2023

Academic Institutions and Nonprofits only

#179776

SPLINTR (Single-cell Profiling and LINeage TRacing) is a high diversity lentiviral barcode library for tracing clonal lineages using bulk and single-cell readouts.

Mark Dawson

Fennell et al Nature. 2022 Jan;601(7891):125-131. doi:

May 11, 2022

Academic Institutions and Nonprofits only

#179775

SPLINTR (Single-cell Profiling and LINeage TRacing) is a high diversity lentiviral barcode library for tracing clonal lineages using bulk and single-cell readouts.

Mark Dawson

Fennell et al Nature. 2022 Jan;601(7891):125-131. doi:

May 11, 2022

Academic Institutions and Nonprofits only

#179774

SPLINTR (Single-cell Profiling and LINeage TRacing) is a high diversity lentiviral barcode library for tracing clonal lineages using bulk and single-cell readouts.

Mark Dawson

Fennell et al Nature. 2022 Jan;601(7891):125-131. doi:

May 11, 2022

Academic Institutions and Nonprofits only

#224585

Pyrrolysine tRNA synthetase library to generate new genetic code expansion (GCE) systems for site-specific incorporation of non-canonical amino acids (ncAAs) into proteins.

Ryan Mehl

Avila-Crump et al ACS Chem Biol. 2022 Dec 16;17(12):3458-3

Jan. 6, 2025

Academic Institutions and Nonprofits only

#104055-AAV2

Ready-to-use AAV2 particles produced from pAAV-CAG-eYFP (#104055). In addition to the viral particles, you will also receive purified pAAV-CAG-eYFP plasmid DNA. CAG-driven eYFP expression control. These AAV preparations are suitable purity for injection into animals.

Viviana Gradinaru

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

June 13, 2023

Academic Institutions and Nonprofits only

#117382-AAV9

Ready-to-use AAV9 particles produced from pAAV-hSyn1-eYFP (#117382). In addition to the viral particles, you will also receive purified pAAV-hSyn1-eYFP plasmid DNA. hSyn-driven eYFP expression. These AAV preparations are suitable purity for injection into animals.

Viviana Gradinaru

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

Jan. 6, 2022

Academic Institutions and Nonprofits only

#99118-AAV2

Ready-to-use AAV2 particles produced from pAAV-CAG-tTA (#99118). In addition to the viral particles, you will also receive purified pAAV-CAG-tTA plasmid DNA. CAG-driven expression of tetracycline-controlled transactivator (tTA). These AAV preparations are suitable purity for injection into animals.

Viviana Gradinaru

Chan et al Nat Neurosci. 2017 Aug;20(8):1172-1179.

June 26, 2024

Academic Institutions and Nonprofits only