Human Oligodendrocyte Specific Protein (CLDN11) activation kit by CRISPRa

CAT#: GA103343

CLDN11 CRISPRa kit - CRISPR gene activation of human claudin 11

  See Other Versions


Find the corresponding CRISPRi Inhibitor Kit

USD 1,290.00

2 Weeks*

Size
    • 1 kit

Product Images

Frequently bought together (2)
Rabbit Polyclonal Anti-CLDN11 Antibody
    • 100 ul

USD 345.00


qSTAR qPCR primer pairs against Homo sapiens gene CLDN11
    • 200 reactions

USD 120.00

Other products for "CLDN11"

Specifications

Product Data
Format 3gRNAs, 1 scramble ctrl and 1 enhancer vector
Symbol CLDN11
Locus ID 5010
Kit Components

GA103343G1, Oligodendrocyte Specific Protein gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA103343G2, Oligodendrocyte Specific Protein gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA103343G3, Oligodendrocyte Specific Protein gRNA vector 3 in pCas-Guide-GFP-CRISPRa

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077

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_001185056, NM_005602
Synonyms OSP; OTM
Summary 'This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Aug 2010]'

Other Versions

{0} Product Review(s)

0 Product Review(s) Submit review

Be the first one to submit a review

Product Citations

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.