CCM2 (NM_001029835) Human 3' UTR Clone
CAT#: SC205722
3' UTR clone of cerebral cavernous malformation 2 (CCM2) transcript variant 1 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | CCM2 (NM_001029835) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | C7orf22; OSM; PP10187 |
ACCN | NM_001029835 |
Insert Size | 453 bp |
Sequence Data |
>SC205722 3’UTR clone of NM_001029835
The sequence shown below is from the reference sequence of NM_001029835. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGCTGCAGCATGGACCAGGACTCAGCATGATGGACAGTGGATGGGGGGGCACCCACACCTTCCGCGCAG TCGTCATAGGCCTTCCCAGAAGGAGCTGCCCAGACCTGCGTGTCAGCCCTTGGTGGTGGCCAGGGAGAG GCGCCCGGTGCAGATGGCCCCGGGCGGCCCAGGTCCTCTACTGTGAAGGAGCAGGGAGCTGCCGAGGGA CACGAGCCTCAGTGCGGGGTGGAAGGCTCTTTGCCTTGTCCACCAGGGCTCAGCCAAGCCCTGCAGTGT GTCCCCGCTCGGGGAGGGCCCGGCCGAGCGGGCAGGGAGAGCCAGTCCTGTCGGCTGGGCCCTTGGACG GCTGTCAGTTTTGCACATGATGTTCCTATTGTAACTCTCAGAGACCTTAAAAAGAAGTTTACTGCAATG TGAATAATTTAATCTCTGGTTGCCAAGCAAAAAAAAAAA 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_001029835.2 |
Synonyms | C7orf22; OSM; PP10187 |
Summary | This gene encodes a scaffold protein that functions in the stress-activated p38 Mitogen-activated protein kinase (MAPK) signaling cascade. The protein interacts with SMAD specific E3 ubiquitin protein ligase 1 (also known as SMURF1) via a phosphotyrosine binding domain to promote RhoA degradation. The protein is required for normal cytoskeletal structure, cell-cell interactions, and lumen formation in endothelial cells. Mutations in this gene result in cerebral cavernous malformations. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009] |
Locus ID | 83605 |
MW | 15.4 |
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