TAT (NM_000353) Human 3' UTR Clone

Specifications

Product Data
Product Name	TAT (NM_000353) Human 3' UTR Clone
Vector	pMirTarget
ACCN	NM_000353
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC213748 3’UTR clone of NM_000353 The sequence shown below is from the reference sequence of NM_000353. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAAGGCAGCCAGGAGGAGTGTGATAAATAGGCCTGCATCCATTCTCCTGAGGATGTGTCCCATCTAGGG AAGGCTGGACTAGGCCTTGCGGCTCCTCAGGGACTCAGGTGGCCCTACTGGGAGAGGGGCCTCAAATGC ACCATGTCAAGGGTTCAAGATTGTTCCTGCTTTTCCCCAAGTACAACCACACCCACACTCAGATCCTCC TCATTCACATCGCAGATTCTCCCTTGCTCTGCGCTGCTAGAGTGACTCACTAATTCATTAATCTGCCTC CCTCTCGTAAGATTTCCTTCTTTTTTTCTTGAAAGTACCAGGTGAACAAAGTTTACCAGAAAGCAGTTG AGACAAGAAAATAAGAGCTCAGGATGAGGGAAAAGAAAAAGATTGAGAGAATTTGTGCCCCCAACCATT TCCTCAGACTCTAAGAAAGAACACGCTCTCTCCAGGCAGGTCTGAAGCTCAACTCTCTTATTGCCTCAC TTCAGGTATACCTCACTTTACACAATAGAATTATAACTGGAAAGAAGTTGGGGACACATGTATTTGGTG ATTACATTTTAAACACATTAGGAAAAGTTGCTATTTGAACTTTTTATTGATTTTTGGGGGGAGTAAAGA ATTATTTTGTGATGCAAATAAATATCCTTTAATTGATCGACTTGCCAAATTTAGATTTGTGTGCATCAG GCTTTCTTTTTTTTCTTTTTTTAGAGAAGTTCAATATAAGCTTTTCTTTTCTTTGTTTCTTTCTTTCTT TATTTTGAGATGGAGTCTTGCTCTGTCGCCCATGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAA CCTCCACCTCCTGGGTTCAAGCGATTCTCTTGCCTCAACCTCCCAAGCAGTTGGGACTACAGGCGTGAG CCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGCTGGTCT CAAACTCCTGACCTCAGGCAATCTGCCCGCCTGGGTCTCCTAAAGTACTGGGATTACAGGCGTGAGCCA CCTCGCCCAGCGGCATCAGGCTTTCTTAAAGTGAGAGCACGCCTGTACTAGAGCAAGCAGGAATCAGAG ACCTTCCAGAAATACTACTGTGTAAGGGCCAGAAATATCTTCACTTGTCATTGTTATATAATCATTATT ACTTTTGCTGTAATGTTAATATTGATTTATTAATATATATTATCTTTTCATACATTTTCTAAGAAACAT TTATATTGATAAGATCTTTTATTTTGCCAAGGGCATAAATTATTGTTTTTCTTTTTTTTTTTTTAATAA ATTTCACCAAGTATGGCTCTTCTGTGATGTGTTTTTTTCTCCGTTTGGGAATTTCTAATCCCAGGCACT CCTCAGTCTCATTGTTTCATTACCTATGAGGTTTCATTTACTTCTTTGTAAATGTACTGACTTTTGGAG TTACTTAAGAACCACAGTTCCTAAAACATTTTATTTGGGAGCTCAACTTCTGGCTTCCTACTTACCAAG AGGCAGTAAGTTATAACCTCTGGCCTTTGTCTTTACATTTTCAACTTTCTGGATCCCTAACCTCTGGTC CCAAGTTACTACGCTTGCCTATATCCACTAACCACTCACTAGGTCACAAAGTTGATGGCTCTGGCTTGA CCCAGTGAATGAGAAGTGTCCTAGATGTTTTTTTTTTTTTTTTTTTTTCGCAAATCTTCATAGGCACAG TTGCCTGTTTAATTTTTTCTTCAGCCCTTCCCTTAGAGGAGGGAGCCTTAAGTTACCTTTCAAGGTTGG GGGTTAGGAATCTATCATAACTAGTCTAGAGATTTCTCACCAAGGGAAATTTTCCTTATCTAAAAGAGG AACTTCAGGTCTCAACCCTGCCAGTCACACCCAATTAATGTCCTTCACAAAAATAAACAGCATATGTTC CCTTTCAATTTGAGTTCAGTGAGCTCACAGCAAAATTTACCTTTTAATTTTCTTCAGCAAATCCAAGA 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_000353.3
Summary	This nuclear gene encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible cognitive disability. A regulator gene for tyrosine aminotransferase is X-linked. [provided by RefSeq, Jul 2008]
Locus ID	6898
MW	77.7

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