DFNB31 (WHRN) (NM_001083885) Human 3' UTR Clone

Specifications

Product Data
Product Name	DFNB31 (WHRN) (NM_001083885) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CIP98; DFNB31; PDZD7B; USH2D; WI
ACCN	NM_001083885
Insert Size	704 bp
Sequence Data	Insert Sequence (showhide) >SC209047 3’UTR clone of NM_001083885 The sequence shown below is from the reference sequence of NM_001083885. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTGGTCACTGAGTTCAATGTGATGCTCTAGAGGCCAAGGCCTGAGGGCCTCCCACCACTGCCCAGCCCC TGGTCCCAGTCCCTTTCCACCGTTGGCTTCATCAAGCTCCTTGCGGGGTTGGGGCTGCATGGCCAGGGT GGCAGGAAGACATCCCCCCTCCATCCCAGCCCACTGGACCAGAACTGGGAGAGGAAGAGAGCAGGACAA GGCAGACAGAAGGTCAGGTCAGGAACTGGTGCTGTACTGGGTACACAGTAGGCGCCCAGGACAAGTGGG TTGCAAGACAGGAAGAAAGGAAAAGGAAGGGCAGAGTGCTGGTTTCTCCAGGTTGGGTTGGGGGCACTG CTGTCCCCCCTCCAGCTAGGACCCAGCCCATCCCCAGATGCCTGAGCCTTTGTCCAAAGTGAGGTCACT CGAGAATTCATGGACACGGCCCCCAGTCAGGGGGCATCTTGCAAGACCTTTAGTGCCACAAATAAGCAT CGAGCACCTCCCCATTCACACCCCCATTCCTCCTGGCTCCTTATCCCCCATGGTGTTTATTATTTATTT CCCTCCCCATGCCCCTGGGGACCCCAAGGCCCCAGCTTCCCTCTGCACCCCCAGCCTATCCCAGAGGCC TTGCAGGTGACCAGCAGTGTCATTGTATTTATATACAGAGCTTATGACTTTAATTTTTCAATAAAGAAA TCTGAACAAGGTTA 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_001083885.3
Synonyms	CIP98; DFNB31; PDZD7B; USH2D; WI
Summary	This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
Locus ID	25861
MW	25.5

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