Calretinin (CALB2) (NM_001740) Human 3' UTR Clone

Specifications

Product Data
Product Name	Calretinin (CALB2) (NM_001740) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CAB29; CAL2; CR
ACCN	NM_001740
Insert Size	598 bp
Sequence Data	Insert Sequence (showhide) >SC207763 3’UTR clone of NM_001740 The sequence shown below is from the reference sequence of NM_001740. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATTGTGCTCTGCAGCGAGCCCCCCATGTAAAGTGGGGACGGGGGCTGCTTCTCCACCTCCCCCAAACCC TGCTTCTGCTGCCCTGATGCGTCTACCCAGACTCAGAGACCGTGAGCGCCCCGCCCCCACCCCTACAGC CTGCACACACCTGCCTGCAGAGCAGGAAATGAGAGATAGAGGATGGGCAGCTGGGGGGCTGTCCTGAGC CCCCTGCACCCACCCCTGCCCAGGCAGTCTTTGCTCAGTGGATCACACACATGGAAGGTGATGGGGGCA TGGGTGGAGGGTCCCTAATTCTCTTCGCTGTGATGCATGAGCTCCCTCGCTGTATGATTTAGGCTTCTA TGTCCAACAGAGTGGACTCTTCCCTCTCGCTCCCCTCTGCCGGTCCCCCATGCCACCACCCACCCCAAA CTTCCAGGTTCCATCCACCACCTTGCCAATGGTGTAGCTGTCCTCTCAGAACTCCTGTGTGTGGAAGGC ACCCGCCCTTTCCTTGCCTTCTTTACTCGGCGTGCTCCTTTTCTCTTTGGGTTTCTTGTTTACCAAAGA AGAGTTTACAGACAATAAAATGGAAAGGTCCTGCTGTGGAAACTTA 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_001740.5
Synonyms	CAB29; CAL2; CR
Summary	This gene encodes an intracellular calcium-binding protein belonging to the troponin C superfamily. Members of this protein family have six EF-hand domains which bind calcium. This protein plays a role in diverse cellular functions, including message targeting and intracellular calcium buffering. It also functions as a modulator of neuronal excitability, and is a diagnostic marker for some human diseases, including Hirschsprung disease and some cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2010]
Locus ID	794
MW	22

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