ANO6 (NM_001142679) Human 3' UTR Clone
CAT#: SC206301
3' UTR clone of anoctamin 6 (ANO6) transcript variant 3 for miRNA target validation
Need custom modification / cloning service?
Get a free quote
CNY 4,845.00
货期*
3周
规格
Product images
经常一起买 (2)
Specifications
Product Data | |
Product Name | ANO6 (NM_001142679) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | BDPLT7; SCTS; TMEM16F |
ACCN | NM_001142679 |
Insert Size | 496 bp |
Sequence Data |
>SC206301 3’UTR clone of NM_001142679
The sequence shown below is from the reference sequence of NM_001142679. 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_001142679.2 |
Synonyms | BDPLT7; SCTS; 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 |
Documents
Product Manuals |
FAQs |
Resources
Customer
Reviews
Loading...