CSRP3 (NM_003476) Human 3' UTR Clone

Specifications

Product Data
Product Name	CSRP3 (NM_003476) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CLP; CMD1M; CMH12; CRP3; LMO4; MLP
ACCN	NM_003476
Insert Size	670 bp
Sequence Data	Insert Sequence (showhide) >SC208372 3’UTR clone of NM_003476 The sequence shown below is from the reference sequence of NM_003476. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTTACACAACAAGTGGAAAAGAAAGAATGAAGAGGTGCGCCGTTTCTCAGATTTTTTGCGAGCCTAAAA CACTTGCCAAGTAATCCTGCACAGATCGATACCTTTCCCCAAATAGCCTCTCCTTTGTAGTCGTACATT ATGTGTTTCTCCTCAGAAGTGATCAGGTCTTTACTGAATGTTAGAAGAGGCCTTTGGAAGAAAATTATG TAAAGTTTAATCTATAACAAATGCTTTATTATTTATAATGCTTGGAATGGGAGAGGCAATAAATAAATG TTTTAGTGCTATCTTGTATGGCTCTAGATCTTTTCTTTGAGATAGAAATTTTCAAAAACATAAAGCTAG TTCAAAAAACGAGTTGCAGAGCATATAATAAATTTGGATGTCAACTGAGAAAGGAGTGAGAAGGAAGAA ACAATGCGCAAAGGAAAGCAGTCTTTCAGAATCTGTCAGCCAAGTGTCTTTCTAGTTACTGCTAATGGA GAAGAAAACAGGGGGTCTGGGAGAAAATAGAGAACATGATAGCAAAATCTAAAAGGAAAATCAAAACTA ATAAAATTGCTGAAGAGTTGATCCCTTTGTCCTATCGTGGGGCTTTGTAATGTTACACATCTCGTGAAA ACTCAGAAATGACAATAAAGCGTGGCATTTGCCTCTGTATTATAAATGA 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_003476.5
Synonyms	CLP; CMD1M; CMH12; CRP3; LMO4; MLP
Summary	This gene encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Mutations in this gene are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans. Alternatively spliced transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]
Locus ID	8048
MW	25.7

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