Espin (ESPN) (NM_031475) Human 3' UTR Clone

Specifications

Product Data
Product Name	Espin (ESPN) (NM_031475) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	DFNB36; LP2654; USH1M
ACCN	NM_031475
Insert Size	828 bp
Sequence Data	Insert Sequence (showhide) >SC209986 3’UTR clone of NM_031475 The sequence shown below is from the reference sequence of NM_031475. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTGAAGAAGGGGGACATCGCTAAGTACTAGAGGCCGCAGACTCCTGTCCGCAGCCTCGCAGCTCCGTGG GGCCCTCCGCCCCAGCCCCAGCCAGCCAGGCCCTGGTGGAAAGGCTGGGAGCCGCACAGCCCTCCCCTC CTGCGCTGGAAACCCTCCCTGACCCCCACCCTGGCCCCCCGTATCCCCAGCCCTTGGCAACACTGGAGT GCACACGCCGCCACGGTTGCCCAGAAAAAGTGCCCAAGCTGCTGACGCAAACAACAACAAATGCTGCTT ATTTGCATGCCGACTTACATATATTTGCATGTTCGTTGACTATCAAAGAGTGCAGAGCTCTCCCCAGCC CCGTGGGTGGTGACTTTGTTTTCCTGCGGGGCTCAGCCCCCTCCAGGATGCAGCCCCCTCCCCCGCACC CCGGAACCGGCGTCGCTGGCGCATCCTGGGTGGAGGCAGGCCCCGAGCTCGGGGAAGGGGTTTTCCCTT CCTCTCTGACCCAGATCTGCGCGCGGCCTAGCCCGGGCCTCATTTCTTATCCCCGCCAAGGGTTTCCTC TCAGTCATTTGTTTACCAGAAACATGAAAACTGCCTGTCTGGCCGGGCCGCACTTGTGGCCCCCGGGAC CCCACCTCTGGCCCCACCTCCCTCAAGTCTGCGCCCCGTCCCCAGCCAGACCCACTCGCTGCCGGGACC CTTTCACTGCCCCGGTGGAGTGAATAGAGGATGAGGGGCCCTGACCCTGTGTCTCCAACTGCTGCACCC CATCCCGACCCTGTCTCCGCCACCTCGCAGCCCCATTAAAGCGCTCTCATCTGGGCTCCGGTTCACTCA 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_031475.3
Synonyms	DFNB36; LP2654; USH1M
Summary	This gene encodes a multifunctional actin-bundling protein. It plays a major role in regulating the organization, dimensions, dynamics, and signaling capacities of the actin filament-rich, microvillus-type specializations that mediate sensory transduction in various mechanosensory and chemosensory cells. Mutations in this gene are associated with autosomal recessive neurosensory deafness, and autosomal dominant sensorineural deafness without vestibular involvement. [provided by RefSeq, Nov 2009]
Locus ID	83715
MW	30

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