ANO6 (NM_001142680) Human 3' UTR Clone

Specifications

Product Data
Product Name	ANO6 (NM_001142680) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	MGC104751; TMEM16F
ACCN	NM_001142680
Insert Size	496 bp
Sequence Data	Insert Sequence (showhide) >SC206298 3’UTR clone of NM_001142680 The sequence shown below is from the reference sequence of NM_001142680. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TGTTTTTCTGTATCGAATTTCTTAAGTTAGATTTATTCAATAATTCATTCAACAAATATTTGTGTGTCT ATTATGTGGCCAGCATTGTTTCATGTGCTCAAGATAGAGTAGCATTGTTTGGCTCATTAATATTCCAAT ACTGGCATTTAAGACCATTAATTTTCCTCTAAATCGTATTTGAGCTGCAACCCACAAGCTTTTATATGT ATAGTTTTTTGTTGTTGCTATTATTAAAAGTATTTTAGATCCTCCCTTGTTTTGCTTTTCAATCTGAAA TGCCTTCATGCCATTTTAATTTTTAAAAGGTAATTTAATTGAGCCTAATTTCTTTTTCTTTTTTCTTTT TTTTGAGACAGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCAATGCAAGC TCTGCCTCCCAGGTTCACGCCATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCACC ACCATGCCTGGCT 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_001142680.1
Synonyms	MGC104751; TMEM16F
Summary	This gene encodes a multi-pass transmembrane protein that belongs to the anoctamin family. This protein is an essential component for the calcium-dependent exposure of phosphatidylserine on the cell surface. The scrambling of phospholipid occurs in various biological systems, such as when blood platelets are activated, they expose phosphatidylserine to trigger the clotting system. Mutations in this gene are associated with Scott syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2011]
Locus ID	196527
MW	18.7

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