Mouse Klc1 activation kit by CRISPRa

CAT#: GA202324

Klc1 CRISPRa kit - CRISPR gene activation of mouse kinesin light chain 1

Product Images

Specifications

Product Data

• Format: 3gRNAs, 1 scramble ctrl and 1 enhancer vector
• Symbol: Klc1
• Locus ID: 16593
• Kit Components:

  GA202324G1, Klc1 gRNA vector 1 in pCas-Guide-CRISPRa

  GA202324G2, Klc1 gRNA vector 2 in pCas-Guide-CRISPRa

  GA202324G3, Klc1 gRNA vector 3 in pCas-Guide-CRISPRa

  1 CRISPRa-Enhancer vector, SKU GE100056

  1 CRISPRa scramble vector, SKU GE100058

• Disclaimer: The kit is designed based on the best knowledge of CRISPa SAM technology. The efficiency of the activation can be affected by many factors, including nucleosome occupancy status, chromatin structure and the gene expression level of the target, etc.

Reference Data

• RefSeq: NM_001025358, NM_001025359, NM_001025360, NM_001025361, NM_001025362, NM_001025363, NM_001081959, NM_008450, NM_001361605, NM_001361609, NM_001361610, NM_001361611, NM_001361612, NM_001361613, NM_001361614
• Synonyms: AI874768; Kns2
• Summary: Conventional kinesin is a tetrameric molecule composed of two heavy chains and two light chains, and transports various cargos along microtubules toward their plus ends. The heavy chains provide the motor activity, while the light chains bind to various cargos. This gene encodes a member of the kinesin light chain family. It associates with kinesin heavy chain through an N-terminal domain, and six tetratricopeptide repeat (TPR) motifs are thought to be involved in binding of cargos such as vesicles, mitochondria, and the Golgi complex. Thus, kinesin light chains function as adapter molecules and not motors per se. Although previously named "kinesin 2", this gene is not a member of the kinesin-2 / kinesin heavy chain subfamily of kinesin motor proteins. Extensive alternative splicing produces isoforms with different C-termini that are proposed to bind to different cargos; however, the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]