We narrowed to 14,121 results for: CAN

#194715

Bicistronic vector expressing CMV promoter driven AsCpf1, and U6 promoter driven guide RNA that can be cloned with BbsI sites

Rudolf Jaenisch

Ma et al Bio Protoc. 2024 Nov 20;14(22):e5108. do

Jan. 5, 2023

Academic Institutions and Nonprofits only

#235773

Plasmid used for constructing donor DNA for TP901-compatible p1 integration. This plasmid is a sfGFP dropout plasmid where sfGFP can be replaced by GOIs using Golden Gate Assembly.

Chang Liu

Pisera et al ACS Synth Biol. 2025 Apr 18;14(4):1002-1

May 5, 2025

Academic Institutions and Nonprofits only

#84881

Empty concatmer vector in which 4 gRNAs can be inserted

Bon-Kyoung Koo

Andersson-Rolf et al Dev Biol. 2016 Oct 27. pii: S0012-1606(1

June 12, 2017

Academic Institutions and Nonprofits only

#102664

Tetracycline inducible expression of GFPmut2 using bicistronic autoregulation; strong ribosome binding site; GFPmut2 ORF can be replaced with gene of interest by isothermal assembly

Zach Hensel

Hensel et al PLoS One. 2017 Oct 30;12(10):e0187259. d

Dec. 1, 2017

Academic Institutions and Nonprofits only

#185594

Control lentivector that can be used to express inserts from the PGK promoter and/or shRNA cassettes from U6.

Jarrod Johnson

Greiner et al Curr Protoc. 2022 Aug;2(8):e514. doi: 10

Aug. 23, 2022

Academic Institutions and Nonprofits only

#216389

this vector can be used to make modRNA expressing Cas9 and p53DD

Xiaojun Lian

Haideri et al Stem Cell Reports. 2024 May 14;19(5):744

April 10, 2024

Academic Institutions and Nonprofits only

#210212

An empty gRNA expression vector to clone U6 promoter driven sgRNAs with gRNA scaffold and with co-expression of DsRed. sgRNA can be cloned by Golden Gate Assembly or restriction digestion using BbsI.

Albert Jeltsch

Rajaram et al Methods Mol Biol. 2024;2842:179-192. doi

Dec. 5, 2023

Academic Institutions and Nonprofits only

#206047

this mini-donor knockin vector can be used to knock nuclear EGFP into NKX6.1 locus

Xiaojun Lian

Haideri et al Stem Cell Reports. 2024 May 14;19(5):744

April 5, 2024

Academic Institutions and Nonprofits only

#134451

Empty concatemer vector in which 2 sgRNAs can be inserted; with Cas9 + Puro

Daniel Stange

Gaebler et al J Vis Exp. 2020 Feb 18;(156). doi: 10.37

Jan. 21, 2020

Academic Institutions and Nonprofits only

#85586

An empty sgRNA expression vector. sgRNA sequence can be cloned into its Bbs I site. Its gRNA scaffold has efficient ver. 2 structure.

Hodaka Fujii

Fujita et al Sci Rep. 2016 Jul 28;6:30485. doi: 10.10

Dec. 5, 2016

Academic Institutions and Nonprofits only