We narrowed to 14,112 results for: CAN

#108455

This plamid can be used to recombine the iTol2-Amp-γ-crystallin:RFP into a BAC.

Nadia Mercader Huber

Sanchez-Iranzo et al Nat Commun. 2018 Jan 30;9(1):428. doi: 1

Sept. 25, 2018

Academic Institutions and Nonprofits only

#102844

Can be used as PCR template for a STAgR reaction

Stefan Stricker

Breunig et al PLoS One. 2018 Apr 27;13(4):e0196015. do

Feb. 6, 2019

Academic Institutions and Nonprofits only

#219928

PrTPI with the overhangs for SapI restriction site can be insert into the base plasmid of TUNEYALI

Irina Borodina

Jiang et al Proc Natl Acad Sci U S A. 2025 Jun 10;12

June 11, 2024

Academic Institutions and Nonprofits only

#133041

SiC-V1 vector with SpCas9 gene and dTomato reporter. sgRNA targeting a gene of interest can be cloned downstream of U6 promoter.

Sriram Neelamegham

Kelkar et al Mol Ther. 2019 Sep 12. pii: S1525-0016(1

Nov. 26, 2019

Academic Institutions and Nonprofits only

#230996

Protein stability reporter construct for transient expression in mammalian cells. Stability of N-terminal GFP-fusion protein can be assessed by flow cytometry by normalizing to mCherry expression.

Michael Rape

Manford et al Cell. 2020 Oct 1;183(1):46-61.e21. doi:

Jan. 14, 2025

Academic Institutions and Nonprofits only

#108462

This plamid can be used to recombine the iTol2-Amp-γ-crystallin:RFP into a BAC.

Nadia Mercader Huber

Sanchez-Iranzo et al Proc Natl Acad Sci U S A. 2018 Apr 2. pi

Sept. 25, 2018

Academic Institutions and Nonprofits only

#181781

Expresses Y2-ShHELIX containing a nicking Y2 I-AniI fusion to ShTnsB. New sgRNA spacer sequences can be added using Golden Gate assembly (via SapI sites).

Benjamin Kleinstiver

Tou et al Nat Biotechnol. 2023 Jan 2. doi: 10.1038

Feb. 16, 2022

Academic Institutions and Nonprofits only

#102841

Can be used as PCR template for a STAgR reaction

Stefan Stricker

Breunig et al PLoS One. 2018 Apr 27;13(4):e0196015. do

May 24, 2019

Academic Institutions and Nonprofits only

#62894

Trojan-Gal4 Expression Module in Phase 2. Insert T2A-Gal4 to genomic loci using the Crispr/Cas technology. Can be converted by cassette exchange into other Trojan exons

Benjamin White

Diao et al Cell Rep. 2015 Mar 3;10(8):1410-21. doi:

May 1, 2015

Academic Institutions and Nonprofits only

#102992

Can be used as backbone for a STAgR reaction

Stefan Stricker

Breunig et al PLoS One. 2018 Apr 27;13(4):e0196015. do

Feb. 6, 2019

Academic Institutions and Nonprofits only