PMP70 (ABCD3) (NM_001122674) Human 3' UTR Clone

Specifications

Product Data
Product Name	PMP70 (ABCD3) (NM_001122674) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	ABC43; CBAS5; PMP70; PXMP1; ZWS2
ACCN	NM_001122674
Insert Size	203 bp
Sequence Data	Insert Sequence (showhide) >SC201473 3’UTR clone of NM_001122674 The sequence shown below is from the reference sequence of NM_001122674. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGGTACTTGGAAAAATTTTGTGGCATTAAAAACCAGACAAATGTATTGGCCAGGCGTGGTGGCTCATG CCTGTAATCCCAGCACTTTGGGAGGCTGAGATGGGAGGATCGCTTGAATCCAGGAGTTCGAGACAAGCC TGGACAAAAAGCGAGACCCGCTTCTTTAAAAAATAATAATAAAACAGAAGTTCTTAAACCATGAA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_001122674.2
Synonyms	ABC43; CBAS5; PMP70; PXMP1; ZWS2
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. This peroxisomal membrane protein likely plays an important role in peroxisome biogenesis. Mutations have been associated with some forms of Zellweger syndrome, a heterogeneous group of peroxisome assembly disorders. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]
Locus ID	5825
MW	7.8

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