We narrowed to 14,101 results for: ckb

#204624

Cloning vector for SSA vector (EGxxFP), the target sequence can be inserted by In-Fusion reaction after AfeI digestion

Akitsu Hotta

Kita et al Stem Cell Reports. 2023 Sep 12;18(9):175

Sept. 27, 2023

Academic Institutions and Nonprofits only

#74826

Gateway cloning compatible binary vector for C-terminal fusion with eYFP (no promoter).

Tsuyoshi Nakagawa

Nakagawa et al Biosci Biotechnol Biochem. 2007 Aug;71(8

Sept. 29, 2016

Academic Institutions and Nonprofits only

#72343

Mammalian expression of secreted mMBP-fused proteins with C-terminal 6His-tag/Strep-tag II/HA-tag

Luca Jovine

Bokhove et al J Struct Biol. 2016 Feb 3. 194:1-7. pii

Feb. 17, 2016

Academic Institutions and Nonprofits only

#160509

Rescue mfn2 knockdown by tethering mitochondria and ER with GFP

Qing Deng

Zhou et al J Cell Sci. 2020 Sep 4;133(17). pii: jcs

Nov. 17, 2020

Academic Institutions and Nonprofits only

#105074

Yeast mating-based Split Ubiquitin Assay, bait vector for in vivo cloning

Wolf Frommer

Obrdlik et al Proc Natl Acad Sci U S A. 2004 Aug 17;10

Feb. 26, 2018

Academic Institutions and Nonprofits only

#75162

Derived from LentiCRISPR v1 but expresses RFP657 instead of puromycin resistance

Beat Bornhauser

McComb et al Sci Transl Med. 2016 May 18;8(339):339ra

May 17, 2016

Academic Institutions and Nonprofits only

#164167

Expresses mCherry2 under the control of CMV promoter, basic vector for AAV, pAAV-CMV backbone, multiclonig site at C terminal

Isei Tanida

Tanida et al Sci Rep. 2020 Dec 14;10(1):21871. doi: 1

March 29, 2021

Academic Institutions and Nonprofits only

#89576

caCas9 integrating vector into the Neut5L locus

George Church

Shapiro et al Nat Microbiol. 2018 Jan;3(1):73-82. doi:

Oct. 2, 2017

Academic Institutions and Nonprofits only

#74852

Gateway cloning compatible binary vector for C-terminal fusion with FLAG (no promoter).

Tsuyoshi Nakagawa

Nakagawa et al Biosci Biotechnol Biochem. 2007 Aug;71(8

Sept. 30, 2016

Academic Institutions and Nonprofits only

#208830

HDR Universal Surrogate Reporter with a sgRNA and consistently expressed eGFP but without Cas9. The selective PuroR reporter gene was designed to be repaired only by the sgRNA/Cas9-triggered HDR.

Zhiying Zhang

Yan et al Mol Ther Nucleic Acids. 2020 Mar 6;19:77

Nov. 16, 2023

Academic Institutions and Nonprofits only