FATP2 (SLC27A2) (NM_001159629) Human 3' UTR Clone

Specifications

Product Data
Product Name	FATP2 (SLC27A2) (NM_001159629) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	ACSVL1; FACVL1; FATP2; hFACVL1; HsT17226; VLACS; VLCS
ACCN	NM_001159629
Insert Size	319 bp
Sequence Data	Insert Sequence (showhide) >SC204121 3’UTR clone of NM_001159629 The sequence shown below is from the reference sequence of NM_001159629. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCCATAAGTGCTAAAACCCTGAAACTCTGAATATTCCCAGGAGGATAACTCAACATTTCCAGAAAGAAA CTGAATGGACAGCCACTTGATATAATCCAACTTTAATTTGATTGAAGATTGTGAGGAAATTTTGTAGGA AATTTGCATACCCGTAAAGGGAGACTTTTTTAAATAACAGTTGAGTCTTTGCAAGTAAAAAGATTTAGA GATTATTATTTTTCAGTGTGCACCTACTGTTTGTATTTGCAAACTGAGCTTGTTGGAGGGAAGGCATTA TTTTTTAAAATACTTAGTAAATTAAATGAACACCAACATGTGA 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_001159629.2
Synonyms	ACSVL1; FACVL1; FATP2; hFACVL1; HsT17226; VLACS; VLCS
Summary	The protein encoded by this gene is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes, but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009]
Locus ID	11001
MW	12.2

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