CC2D2A (NM_001080522) Human 3' UTR Clone

Specifications

Product Data
Product Name	CC2D2A (NM_001080522) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	COACH2; JBTS9; MKS6
ACCN	NM_001080522
Insert Size	179 bp
Sequence Data	Insert Sequence (showhide) >SC201386 3’UTR clone of NM_001080522 The sequence shown below is from the reference sequence of NM_001080522. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TATGTTGCCTCTCTTATACGCAACAGGTAATTTTTTTCACTGTACTTTCTGTATCATGTAAAAACTACA CTTAGGATATGAGAAAATTTTAAATTATATGCATCACATCAGAAGAACATATTATTGGCAAATAATAAA ATTATCAACTGTTTTCAAACTGTGAAAAAAAAAAAAAAAAA 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_001080522.2
Synonyms	COACH2; JBTS9; MKS6
Summary	This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Locus ID	57545
MW	7.1

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