Occludin (OCLN) (NM_002538) Human 3' UTR Clone

Specifications

Product Data
Product Name	Occludin (OCLN) (NM_002538) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BLCPMG; PPP1R115; PTORCH1
ACCN	NM_002538
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC208413 3’UTR clone of NM_002538 The sequence shown below is from the reference sequence of NM_002538. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTTGGAGACTATGATAGACAGAAAACATAGAAGGCTGATGCCAAGTTGTTTGAGAAATTAAGTATCTGA CATCTCTGCAATCTTCTCAGAAGGCAAATGACTTTGGACCATAACCCCGGAAGCCAAACCTCTGTGAGC ATCACAAAGTTTTGGTTGCTTTAACATCATCAGTATTGAAGCATTTTATAAATCGCTTTTGATAATCAA CTGGGCTGAACACTCCAATTAAGGATTTTATGCTTTAAACATTGGTTCTTGTATTAAGAATGAAATACT GTTTGAGGTTTTTAAGCCTTAAAGGAAGGTTCTGGTGTGAACTAAACTTTCACACCCCAGACGATGTCT TCATACCTACATGTATTTGTTTGCATAGGTGATCTCATTTAATCCTCTCAACCACCTTTCAGATAACTG TTATTTATAATCACTTTTTTCCACATAAGGAAACTGGGTTCCTGCAATGAAGTCTCTGAAGTGAAACTG CTTGTTTCCTAGCACACACTTTTGGTTAAGTCTGTTTTATGACTTCATTAATAATAAATTCCCTGGCCT TTCATATTTTAGCTACTATATATGTGATGATCTACCAGCCTCCCTATTTTTTTTCTGTTATATAAATGG TTAAAAGAGGTTTTTCTTAAATAATAAAGATCATGTAAAAGTAACAAATGTGTGAAATTTAAAGATTGT AAATATATATTTACTTTTTTAAGATCAAAGTTTAAACCCCGTGGTTAGAATTTTGTGTGTTTTTAAATA CTTTTTATCTTTTTGCATGCCTTTTTTAAAAAACCAACTAGAACTTTTCATTATATCAGAATATCTGAT TACATTTATAATTCAATTGTGACTTGAACTGTATCTTACAGGAATGTTCAATTTCTATACATATTTTAT AAGGTATTAAACCTGGTGTTTTCTTTCCATAATAACCTGTTTGATGTTATTAGTGCTGTTAACATACAG CAATGGAAAACCACACTCAGGAGTTGTATCTGTTGTTGTTTATACTCCTTTGGATGCTGTGCTGGTTAG TCGTTTCCCATTCCTTTGGCTGTAAGAATGCTGATATGTCTGGGAATAGAATGCTATACCACGAAATAC CAAATAATTTCAAATGGTGCCCTTAAATTGTATCACTTTTTTAAAAATTCAGATTCTTATTAGTAAAAT TAGTTGATAGCACTGTGCTGACCAAGTTGATTGTGATCATCCCAGCTTAGACTTTTCTAAAAACTTTTT TTTAGAATAATCTATAAACTGAACTTTAGTATGCATTTCAGATATTTAGGTATATAATTTTTTTTTTTT TTTGAGACAGAGTCTCACTCTCACCCAGGCTGGAATGCAGTGGTGCTATCTTGGCTCACTGCAACCTCC ACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCTCGAGTAGTTGAGACTACAGGTGCCCATCACC ATGCGTGGCTAATTTTTGTATTTTTAATAGAGACGGGGTTTTACCATAGTGGCCAGGTTGGTCTTGAAC TCCTGACCTTGTGGTCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCC TGGCCTAAGTGTGTGTGTGTGTGTGTGTGTGTATTTTTTTTTTTTTTTTTTTGAGATGGAGTTTTGCTC TTGTTGAACAGGCTGGAGTGCAATGTCGCGATCTCAGCTCACCACAACCTCCGCCTCCCAGGTTCAAAC AATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCCACCACACCTGGCTAATTTTT TTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCTCAG GTGATCCATCCACCTCGGCCTCCCAAAGTGCTGGGATTAGAGGCGTGAGCCACTGTGCCCGGCCTATAA TTTTTGATAGATGATTTTGAATTATTTTCCAGAGATAAAATTTTAAATGTTTCCATTATATCACTGAT 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_002538.4
Synonyms	BLCPMG; PPP1R115; PTORCH1
Summary	This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5. [provided by RefSeq, Apr 2011]
Locus ID	100506658
MW	77

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