Human ABCD2 activation kit by CRISPRa

CAT#: GA100160

ABCD2 CRISPRa kit - CRISPR gene activation of human ATP binding cassette subfamily D 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)
ABCD2 mouse monoclonal antibody,clone OTI3B7
    • 100 ul

CN¥ 1,999.00
CN¥ 2,700.00


ABCD2 (Myc-DDK-tagged)-Human ATP-binding cassette, sub-family D (ALD), member 2 (ABCD2)
    • 10 ug

CN¥ 5,424.00
CN¥ 5,800.00


ABCD2 mouse monoclonal antibody,clone OTI3B7
    • 30 ul

CN¥ 800.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol ABCD2
Locus ID 225
Kit Components

GA100160G1, ABCD2 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA100160G2, ABCD2 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA100160G3, ABCD2 gRNA vector 3 in pCas-Guide-GFP-CRISPRa

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077

Reference Data
RefSeq NM_005164
Synonyms ABC39; ALDL1; ALDR; ALDRP; hALDR
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 ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. The function of this peroxisomal membrane protein is unknown; however this protein is speculated to function as a dimerization partner of ABCD1 and/or other peroxisomal ABC transporters. Mutations in this gene have been observed in patients with adrenoleukodystrophy, a severe demyelinating disease. This gene has been identified as a candidate for a modifier gene, accounting for the extreme variation among adrenoleukodystrophy phenotypes. This gene is also a candidate for a complement group of Zellweger syndrome, a genetically heterogeneous disorder of peroxisomal biogenesis. [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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