GJB3 (NM_024009) Human 3' UTR Clone

Specifications

Product Data
Product Name	GJB3 (NM_024009) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CX31; DFNA2; DFNA2B; EKV; EKVP1
ACCN	NM_024009
Insert Size	819 bp
Sequence Data	Insert Sequence (showhide) >SC209917 3’UTR clone of NM_024009 The sequence shown below is from the reference sequence of NM_024009. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCTTCAGCACCCAACCTGACCCCCATCTGACCACAGGGCAGGGGTGGGGCAACATGCGGGCTGCCAATG GGACATGCAGGGCGGTGTGGCAGGTGGAGAGGTCCTACAGGGGCTGAGTGACCCCACTCTGAGTTCACT AAGTTATGCAACTTTCGTTTTGGCAGATATTTTTTGACACTGGGAACTGGGCTGTCTAGCCGGGTATAG GTAACCCACAGGCCCAGTGCCAGCCCTCAAAGGACATAGACTTTGAAACAAGCGAATTAACTATCTACG CTGCCTGCAAGGGGCCACTTAGGGCACTGCTAGCAGGGCTTCAACCAGGAAGGGATCAACCCAGGAAGG GATGATCAGGAGAGGCTTCCCTGAGGACATAATGTGTAAGAGAGGTGAGAAGTGCTCCCAAGCAGACAC AACAGCAGCACAGAGGTCTGGAGGCCACACAAAAAGTGATGCTCGCCCTGGGCTAGCCTCAGCAGACCT AAGGCATCTCTACTCCCTCCAGAGGAGCCGCCCAGATTCCTGCAGTGGAGAGGAGGTCTTCCAGCAGCA GCAGGTCTGGAGGGCTGAGAATGAACCTGACTAGAGGTTCTGGAGATACCCAGAGGTCCCCCAGGTCAT CACTTGGCTCAGTGGAAGCCCTCTTTCCCCAAATCCTACTCCCTCAGCCTCAGGCAGTGGTGCTCCCAT CTTCCTCCCCACAACTGTGCTCAGGCTGGTGCCAGCCTTTCAGACCCTGCTCCCAGGGACTTGGGTGGA TGCGCTGATAGAACATCCTCAAGACAGTTTCCTTGAAATCAATAAATACTGTGTTTTATA 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_024009.3
Synonyms	CX31; DFNA2; DFNA2B; EKV; EKVP1
Summary	This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene can cause non-syndromic deafness or erythrokeratodermia variabilis, a skin disorder. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
Locus ID	2707
MW	29.9

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