SARS2 (NM_017827) Human 3' UTR Clone

Specifications

Product Data
Product Name	SARS2 (NM_017827) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	mtSerRS; SARS; SARSM; SerRS; SerRSmt; SERS; SYS
ACCN	NM_017827
Insert Size	370 bp
Sequence Data	Insert Sequence (showhide) >SC204832 3’UTR clone of NM_017827 The sequence shown below is from the reference sequence of NM_017827. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGGCTGCCTGGCCAGCCTGCTGTAAGCTAAGAACCCACCCACAGCAGCCCTCGGGGGTGTCACTGCTTC CTGGAGTTCAGGAGACCCCGGACACCTGGGACCTGTGTTGCTGAGCCCGTCCTGACATCTGTGTTCTTC CTGTCAGCTCCACGCCCGGGCCCCTGGACCACGGGGTCCACCTCTCCTCTGTCCTTGCTGCCTCAGAGT CAGTCACTGACCCTGTTATCATTGAGGGTCCCAGTGGGAAGCAGGACGTCTGGGCTTTACGGTTCTAGG GACAGGAGAAGCAGAGGAAGAGGCTTCCATCCCTCCTTCCTTCTTTCCTCCTACAGTGCTGAGCAAAAA GTCCCCAATAAATGGTCAGGACAAA 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_017827.4
Synonyms	mtSerRS; SARS; SARSM; SerRS; SerRSmt; SERS; SYS
Summary	This gene encodes the mitochondrial seryl-tRNA synthethase precursor, a member of the class II tRNA synthetase family. The mature enzyme catalyzes the ligation of Serine to tRNA(Ser) and participates in the biosynthesis of selenocysteinyl-tRNA(sec) in mitochondria. The enzyme contains an N-terminal tRNA binding domain and a core catalytic domain. It functions in a homodimeric form, which is stabilized by tRNA binding. This gene is regulated by a bidirectional promoter that also controls the expression of mitochondrial ribosomal protein S12. Both genes are within the critical interval for the autosomal dominant deafness locus DFNA4 and might be linked to this disease. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Mar 2009]
Locus ID	54938
MW	13.3

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