ornithine aminotransferase (OAT) (NM_000274) Human 3' UTR Clone

Specifications

Product Data
Product Name	ornithine aminotransferase (OAT) (NM_000274) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	GACR; HOGA; OATASE; OKT
ACCN	NM_000274
Insert Size	669 bp
Sequence Data	Insert Sequence (showhide) >SC208484 3’UTR clone of NM_000274 The sequence shown below is from the reference sequence of NM_000274. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATTATTAACAAGACCATCTTGTCTTTCTGAGGGTAGCCAGCTGTTTTCAGTGGTCCCTGGGAGCCAGCT GGAGACAGGTGGTCCTGTAAAAGCTTTATTCCTAATGTGGGCACATTCCACTCCCATGAGTCTTCAAAA ACTTTTTTTTTGAATATATTTTTTTCAGTTGATACATAATAGAACAACGTTTATGAACCTGCCGTTTGC TTTGTAACGTAACTAAATAATGTAATGGCATCTATATTCAGTTGAAGTGTTTTGATGTGCATGTGTACT TCCTAAGGTGAAATGCATCTATATACAGACAGCCTCTAAATCAAGTCCTTCAGTATAATTGATATATGT TTTTATAATTTCCTCACTGGTATAAGTGTTTCATATTTGAAAAAGTTATCTCTGGGTATTGCATAAAAG GCTTCATCTTATAAAGTGAAATCATTGTTATTGAATTTTAGGAAGGATTAATGGTTAAGTGTATATAAA ATACTAATATTAAGTAAACTTCATATTGGCCAACACCAGGGTTGTATTCTATGGATGTCATTATTTTGA ATTAAGAATTAGTGTTTAACATTCCTAAATTGTTTTGAGTGCTTGATTATAATTTGTAAAAAATGTTTA TTTTCAATACTTCTTTAAATTTAAAATAAAGCTTATATTTCAAATGTC 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_000274.4
Synonyms	GACR; HOGA; OATASE; OKT
Summary	This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. Alternatively spliced transcript variants encoding different isoforms have been described. Related pseudogenes have been defined on the X chromosome. [provided by RefSeq, Jan 2010]
Locus ID	4942
MW	25.3

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