ACOX2 (NM_003500) Human 3' UTR Clone

Specifications

Product Data
Product Name	ACOX2 (NM_003500) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BCOX; BRCACOX; BRCOX; CBAS6; THCCox
ACCN	NM_003500
Insert Size	118 bp
Sequence Data	Insert Sequence (showhide) >SC201167 3’UTR clone of NM_003500 The sequence shown below is from the reference sequence of NM_003500. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTTTTACAAAGTTGGAGATCCAAGCTATGAAATAACCAACAGTATTCAAGAAGCAACCAGCACCATCAT GTGATAATGGTACTATGGCATATATGCAACATTAAAATTTTAAATTAGA 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_003500.4
Synonyms	BCOX; BRCACOX; BRCOX; CBAS6; THCCox
Summary	The product of this gene belongs to the acyl-CoA oxidase family. It encodes the branched-chain acyl-CoA oxidase which is involved in the degradation of long branched fatty acids and bile acid intermediates in peroxisomes. Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates, and may lead to Zellweger syndrome, severe cognitive disability, and death in children. [provided by RefSeq, Mar 2009]
Locus ID	8309
MW	4.7

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