TPM1 (NM_001018008) Human 3' UTR Clone
CAT#: SC208932
3' UTR clone of tropomyosin 1 (alpha) (TPM1) transcript variant 6 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 | TPM1 (NM_001018008) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | C15orf13; CMD1Y; CMH3; HEL-S-265; HTM-alpha; LVNC9; TMSA |
ACCN | NM_001018008 |
Insert Size | 2000 bp |
Sequence Data |
>SC208932 3’UTR clone of NM_001018008
The sequence shown below is from the reference sequence of NM_001018008. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAACTAAAGCTGGCCCTGAATGAGGATTAAACTTAAGAGTGAAAAAACTTGGGCTGAATTCTAGGCGTG GAGCCCATGTGCAGAAAATCTAAGACTGTCCTACCTTCAACTAATAGAGTTGAAAACAGTTGCTTTCTG CAGAAATGCAAATGCAAGGAATTGGCTGAAAGGCTGGCCTTGCCTGCTTGTTTCTCTATATGGCTGGAA TAATTACGTTCTCTTTAATCACAAAACAGCTTTTATGGTAGAATACTTATATCAATTCAGCACTGCTCC TTGAAATAGCAGGTCCTCTTGTTTGAACTGATAAATAATGAGGAGCCCCCCCAAAAAATGTTTTCTATT TCCTGACAGCCATGAGTCCTACTTTAAGTATGTATATATATATATATATGTGTGTGTGTGTGTGTGTGT ATATATTCCTATCAGATACTCATATTCCTAACTTCTAAATATCTGGTATAGTGTTTGAAATATGATTAA ATGTACCTATGCTTGGGCAAAATAGCTTTTGAAAACAGGAACTCATGCCAGAAGCCCCTGGTTGTCTGA AAGGTATGCTTTACTCAGTCTAATGGTGCTGTTGGAGTCTGGGGAGAATGTCATGCTAATAAATAGAAC ACTATAAAAATATTAAGAGAATGTCCTAATGAAGTGTGCATGAAACATGTTGACAATTTTTTATGAGCA ACAGAAATAAATCATTTTAAAAGTTCTCAGAAAACCTATTTATGTCATCTTTGCTTTTGTGAGTTTGTG TTACCGCACAACTCCCAGACTTTTAACTGCCTGTACCTTGGAAATGTCTGCTGTTCGTAACTTCTTCAG TTTGTATAACAGTGCTGCAGCTGTATTTGGTTTTTACCTCTCCCTGTTCCCACGGCACACCGTCAGTGA ACCTTCACCAAACCCCACGTGCATTTTATCCTCAGTGAATTGTTGGTGGAGGTGCACCTGACTGCTCTG TGAGAATCCGTGCCATGGCTCCTTTGGGTCAAAGATGCCCTCCCCTCCGTCTTAGGTTCTTGTCTAGAA ATGAGTAATGTCTTACAAGCATGCCTAGTTCTAATCATCTCATCCTGTGTTTGTGATTGATGTTTGCCT GCCTAAATGTACAAACCACCATTGTGTCCAAAGCACAGCTATTCATGACTTAATTTTCTAATCTCACCA CAGAGAAAGTGGCTCATGCCAAAGAAGAAAACCTTAGTATGCATCAGATGCTGGATCAGACTTTACTGG AGTTAAACAACATGTGAAAACCTCCTTAGCTGCGACCACATTCTTTCGTTTTGTTTTGTTTTGTTTTTA AACACCTGCTTACCCCTTAAATGCAATTTATTTACTTTTACCACTGTCACAGAAACATCCACAAGATAC CAGCTAGGTCAGGGGGTGGGGAAAACACATACAAAAAGGCAAGCCCATGTCAGGGCGATCCTGGTTCAA ATGTGCCATTTCCCGGGTTGATGCTGCCACACTTTGTAGAGAGTTTAGCAACACAGTGTGCTTAGTCAG CGTAGGAATCCTCACTAAAGCAGAAGAAGTTCCATTCAAAGTGCCAATGATAGAGTCAACAGGAAGGTT AATGTTGGAAACACAATCAGGTGTGGATTGGTGCTACTTTGAACAAAAGGTCCCCCTGTGGTCTTTTGT TCAACATTGTACAATGTAGAACTCTGTCCAACACTAATTTATTTTGTCTTGAGTTTTACTACAAGATGA GACTATGGATCCCGCATGCCTGAATTCACTAAAGCCAAGGGTCTGTAAGCCACGCTGCTCTTCCGAGAC TTCCATTCCTTTCTGATTGGCACACGTGCAGCTCATGACAATCTGTAGGATAACAATCAGTGTGGATTT CCACTCTTTTCAGTCCTTCATGTTAAAGATTTAGACACCACATACAACTGGTAAAGGACGTTTTCTTGA GAGTTTTAACTATATGTAAACATTGTATAATGATATGGAATAAAATGCACATTGTAGGACATTTTCTA 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_001018008.2 |
Synonyms | C15orf13; CMD1Y; CMH3; HEL-S-265; HTM-alpha; LVNC9; TMSA |
Summary | This gene is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction. In smooth muscle and non-muscle cells, alternatively spliced transcript variants encoding a range of isoforms have been described. Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008] |
Locus ID | 7168 |
MW | 76.3 |
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