EVC2 (NM_147127) Human 3' UTR Clone

Specifications

Product Data
Product Name	EVC2 (NM_147127) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	LBN; WAD
ACCN	NM_147127
Insert Size	439 bp
Sequence Data	Insert Sequence (showhide) >SC205994 3’UTR clone of NM_147127 The sequence shown below is from the reference sequence of NM_147127. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAGGCCATGAGGGCCTTGGGCATGGACTAGCCCAAGGGAAAGACCTGCGGGAGCATCTGAAGAGAGAAG GGATGATTTTCTCCTGCCCGCCGGTGTTTGTGTGTTTATAATGCACAACTCGCAAATATAAATTGCACA TGCAGAAGGCACAGACCCCGTAGCGCATGCCAACTTGCAGGGACTCGGTTTAATCTTGTCTCATGAATT TCCAGATGGCCCACTCTCTTCCATATCACAAGGACATAAACACTCCTTCTTTCAGCCCCACCTCCCCAG GGCCCTGGAGGAGACCCCCACCCTGCAATCCACACCCCATCCTCTGCTGCAGAAGCTATGGTCTGTGTG GTGACAGCCAGATTCTCTACTCTTATGTTTTGTATTTGTTACATATTCTATTTTTATAAAGGGAATTTT AAAAAATAAATGTGTTTTGCACAAA 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_147127.5
Synonyms	LBN; WAD
Summary	This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Locus ID	132884
MW	16.3

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