Human MRP2 (ABCC2) activation kit by CRISPRa

CAT#: GA100877

ABCC2 CRISPRa kit - CRISPR gene activation of human ATP binding cassette subfamily C member 2



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CN¥ 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (3)
Rabbit polyclonal anti-ABCC2 antibody
    • 100 ul

CN¥ 1,999.00
CN¥ 3,280.00


ABCC2 (Myc-DDK-tagged)-Human ATP-binding cassette, sub-family C (CFTR/MRP), member 2 (ABCC2)
    • 10 ug

CN¥ 15,856.00


Rabbit Polyclonal anti-ABCC2 Antibody
    • 30 ul

CN¥ 800.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol ABCC2
Locus ID 1244
Kit Components

GA100877G1, MRP2 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA100877G2, MRP2 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA100877G3, MRP2 gRNA vector 3 in pCas-Guide-GFP-CRISPRa

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077

Reference Data
RefSeq NM_000392
Synonyms ABC30; CMOAT; cMRP; DJS; MRP2
Summary The 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 MRP subfamily which is involved in multi-drug resistance. This protein is expressed in the canalicular (apical) part of the hepatocyte and functions in biliary transport. Substrates include anticancer drugs such as vinblastine; therefore, this protein appears to contribute to drug resistance in mammalian cells. Several different mutations in this gene have been observed in patients with Dubin-Johnson syndrome (DJS), an autosomal recessive disorder characterized by conjugated hyperbilirubinemia. [provided by RefSeq, Jul 2008]
*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.

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