PCDH11X (NM_014522) Human 3' UTR Clone

Specifications

Product Data
Product Name	PCDH11X (NM_014522) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	PCDH-X; PCDH11; PCDHX
ACCN	NM_014522
Insert Size	722 bp
Sequence Data	Insert Sequence (showhide) >SC208973 3’UTR clone of NM_014522 The sequence shown below is from the reference sequence of NM_014522. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGTATCCAAGTTTCTAACACAACTTTCTAACTATTTTTTTATTATTATTTTCAGTTGATGTAGAACTTT ACAAAATCTATTGACTTCAAAGAGGGATCAAAACAATCATATTCTACAGATGTACCCAATAGATATATG GATTCAATTAAGTTTGGTAGAAGATGAGAACAAAATAACTACTGATTTAGGAAAATTGGATGCAGAATA ATAATTATAGTAGGGGCAATTTTGTCTGTAGATGGCAGTATGACAATTCTTGCTAGAGAATATATTGAA AAAAACTTCAACACAAAGGGTTGTAGCACTGTCCTCAGTACCATTGTGTGCATGAGGATCAGAATAGTC TGGGCTAGATACATCACATTAAAGCTTTTCAGAATCTGATAAATAGCTCTAAATACTAATGATATTGAG AAGCCTAGCTTCACTTGGGAAAATCTGTGGCTGTTCACAGAAATTCAGCACCAAGTTATTCCCCCCATA CTCTACCAGGCCTTCAGGTCCTCATAAAGAAAAGTGTCGTTTTCAGATTAGGAACTCAAAATTATTTTG GTGCATCAAATCTACAGTCACACAATATAACAAGAATGGGATTAGAAAAATGAAAGCCTACTCATTCTC ATCTTTAAGCCAGAGAATGAAATATATATGAGGTCTCTGGATAGCTATTTAAATATTTGCATATTTATG CAAGGTATTTTGAGCCCTTCAGAAGACATTCT 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_014522.1
Synonyms	PCDH-X; PCDH11; PCDHX
Summary	This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 7 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene is located in a major X/Y block of homology and its Y homolog, despite divergence leading to coding region changes, is the most closely related cadherin family member. The protein is thought to play a fundamental role in cell-cell recognition essential for the segmental development and function of the central nervous system. Disruption of this gene may be associated with developmental dyslexia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
Locus ID	27328
MW	28.4

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