Human P Glycoprotein (ABCB1) activation kit by CRISPRa

CAT#: GA103521

ABCB1 CRISPRa kit - CRISPR gene activation of human ATP binding cassette subfamily B member 1

Product Images

Specifications

Product Data

• Format: 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
• Symbol: ABCB1
• Locus ID: 5243
• Kit Components:

  GA103521G1, P Glycoprotein gRNA vector 1 in pCas-Guide-GFP-CRISPRa

  GA103521G2, P Glycoprotein gRNA vector 2 in pCas-Guide-GFP-CRISPRa

  GA103521G3, P Glycoprotein gRNA vector 3 in pCas-Guide-GFP-CRISPRa

  1 CRISPRa-Enhancer vector, SKU GE100056

  1 CRISPRa scramble vector, SKU GE100077

• Disclaimer: These products are manufactured and supplied by OriGene under license from ERS. The kit is designed based on the best knowledge of CRISPRa 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_000927, NM_001348944, NM_001348945, NM_001348946
• UniProt ID: P08183
• Synonyms: ABC20; CD243; CLCS; GP170; MDR1; P-GP; PGY1
• Summary: The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is an ATP-dependent drug efflux pump for xenobiotic compounds with broad substrate specificity. It is responsible for decreased drug accumulation in multidrug-resistant cells and often mediates the development of resistance to anticancer drugs. This protein also functions as a transporter in the blood-brain barrier. Mutations in this gene are associated with colchicine resistance and Inflammatory bowel disease 13. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Feb 2017]