TJP2 (NM_201629) Human 3' UTR Clone

Specifications

Product Data
Product Name	TJP2 (NM_201629) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	C9DUPq21.11; DFNA51; DUP9q21.11; FHCA1; PFIC4; X104; ZO2
ACCN	NM_201629
Insert Size	865 bp
Sequence Data	Insert Sequence (showhide) >SC210301 3' UTR clone of NM_201629 The sequence shown below is from the reference sequence of NM_201629. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC GCCAGTCTGCCCGATACCGGGACACAGAATTATAGATGTCTGAGCACGGACTCTCCCAGGCCTGCCTGCA TGGCATCAGACTAGCCACTCCTGCCAGGCCGCCGGGATGGTTCTTCTCCAGTTAGAATGCACCATGGAGA CGTGGTGGGACTCCAGCTCGTGTGTCCTCATGGAGAACCCAGGGGACAGCTGGTGCAAATTCAGAACTGA GGGCTCTGTTTGTGGGACTGGGTTAGAGGAGTCTGTGGCTTTTTGTTCAGAATTAAGCAGAACACTGCAG TCAGATCCTGTTACTTGCTTCAGTGGACCGAAATCTGTATTCTGTTTGCGTACTTGTAATATGTATATTA AGAAGCAATAACTATTTTTCCTCATTAATAGCTGCCTTCAAGGACTGTTTCAGTGTGAGTCAGAATGTGA AAAAGGAATAAAAAATACTGTTGGGCTCAAACTAAATTCAAAGAAGTACTTTATTGCAACTCTTTTAAGT GCCTTGGATGAGAAGTGTCTTAAATTTTCTTCCTTTGAAGCTTTAGGCAGAGCCATAATGGACTAAAACA TTTTGACTAAGTTTTTATACCAGCTTAATAGCTGTAGTTTTCCCTGCACTGTGTCATCTTTTCAAGGCAT TTGTCTTTGTAATATTTTCCATAAATTTGGACTGTCTATATCATAACTATACTTGATAGTTTGGCTATAA GTGCTCAATAGCTTGAAGCCCAAGAAGTTGGTATCGAAATTTGTTGTTTGTTTAAACCCAAGTGCTGCAC AAAAGCAGATACTTGAGGAAAACACTATTTCCAAAAGCACATGTATTGACAACAGTTTTATAATTTAATA AAAAGGAATACATTGCAATCCGTAA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
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_201629.2
Synonyms	C9DUPq21.11; DFNA51; DUP9q21.11; FHCA1; PFIC4; X104; ZO2
Summary	This gene encodes a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutations in this gene have been identified in patients with hypercholanemia, and genomic duplication of a 270 kb region including this gene causes autosomal dominant deafness-51. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]
Locus ID	9414

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