SMCR7 (MIEF2) (NM_001144900) Human 3' UTR Clone
CAT#: SC216112
3' UTR clone of Smith-Magenis syndrome chromosome region candidate 7 (SMCR7) transcript variant 3 for miRNA target validation
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CNY 5795.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | SMCR7 (MIEF2) (NM_001144900) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | COXPD49; MID49; SMCR7 |
ACCN | NM_001144900 |
Insert Size | 2000 bp |
Sequence Data |
>SC216112 3’UTR clone of NM_001144900
The sequence shown below is from the reference sequence of NM_001144900. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTGCTGGGCCGTGCGCAGGACGCAGCTTGAGTTCTGCCCCCGTGGGAGCAGCCCCTGGGACCGCTTCCT GGTCGGGGGCTACCTCTCCTCCCGCGTCCTGCTGGAGCTACTCCGCAAGGCGCTGGCTGCTTCTGTCAA CTGGCCGGCCATTGGCAGCCTTCTCGGGTGCCTGATCCGGCCCAGCATGGCCTCGGAGGAGCTGCTGCT CGAGGTGCAGCACGAACGCCTGGAGCTCACTGTGGCTGTGCTTGTGGCAGTCCCTGGGGTCGATGCTGA CGACCGCCTCCTCTTGGCCTGGCCCCTGGAGGGGCTGGCGGGGAACCTCTGGCTGCAGGACCTGTATCC AGTGGAGGCTGCTAGGCTGCGAGCCCTGGACGACCATGACGCTGGGACTCGCCGGCGGCTGCTGCTGCT GCTGTGTGCTGTCTGCCGTGGTTGCTCGGCTCTGGGGCAGCTAGGCCGGGGTCACCTGACCCAGGTGGT CCTGCGTCTGGGGGAGGACAACGTGGATTGGACGGAGGAGGCCTTGGGTGAGCGCTTCCTGCAAGCCCT GGAGCTGCTCATCGGCAGCCTGGAGCAGGCCAGCCTGCCCTGCCACTTCAACCCCAGCGTGAACCTCTT CAGCAGCTTGCGTGAGGAGGAGATTGACGACATTGGCTATGCGCTATACAGTGGCCTACAGGAGCCCGA GGGGCTGCTCTAGGTGGGTGGAAACGGGTGGTTGCCATGTTTTCTAATGCTGGGGAGCTGCACCCACCT CCCTTCCAGGGATTTGAATAGTGGTTTTTCTCTAGCTTTTTGCCAGAACAAAGGAGGGTACATTACTTA AACCCAGGGCATCAGGATGTGCTTGGGCTATGGTGGCCATAAACCCTGAGCCCAGAGAGCTTGGGTCAC TGTCACCTGAGTGCAGCTGGGCTGCCTCAGGCAGCTTGGAGTGCCAGCCATTCCTGCAAGCACCGTTTC AGCTCTTGGGGCCAACCCCAGGACCTTTGGCTCTGTCCATCACCAGCAACCAATCCACCAACAGAATGT GGTTTCTGCCATCCTGGGCAGAAGCTGAAGGCCAGCTTCACATTTCTGCTGAGAGAAGGTGACTTAACG CCTTTTCCGGCCCTAGCTCCAGGCGTTTTGAGGCGTCTGGTGCCTGATGGTAGGTATGGTGTGTTTGTT CTGTCCCCCAGGGGCTGGAGTCACCTGGTGCCCCTGAAGGACAGATTTTTGGCTGTTAAAGGATGGCAT TTTCCTGCTGTCTTCTGTGCGTTTAGTTTTCTTGCTGAGCGGGAGCTCAGTATGACTTGCCACCCACCT GATACCTCAGGGCAAGGCCCTTTTTCCCTCCAGCCAGGTGAGTGTTTTCTTCAGGCAGCTGAGGGTCCT GGGGGAGCTGAGGCTCTGTGCTGCACCCCCAGCCCACAGCTGGGGCATCTCACTGGAGCTGTTCCAGGC CCCACTGGAGAGCAGAGGACCTGATCCCCCACTAGAGAGGTCCGGTGTGCACAGCCGGCCTCCCAGTGT GCCAAAATGAACTGCTCTCAGCTGATGGCTGTATTCTGACTTTGAAGCCTGTTAAGAGGTAGCAAGGGG GCTAGAGGAGGGAGATTCCACCTCCCCTCCCAAGTGACCCTCCTCCTGCCTCTGGTATCCTTCCTTTTG AAACGAAGCTCAGCTTCGAAGATGTGAACAAGAATAAAAGGAAAAAATTCTAATGTATATATAACTCAG GCTGGATAAGGGAGTCTTGGTGCTTTCATACGCAGCTGTTGAGGGTTTTCTGTAAGTCCTGTGGCTTGT CCTGGCACTTTGGCAAGAGTGCTTGAGGTCAATTGGAGGTGGTAGAGTTTACTTTAAAAAGTAGCATCT TGGCCGGGTGTGGTGGCTCGCATCTGTAATCCCAGCACATCGGGAGGCCGAGGCGGGCGGATCACGAGG TCAAGAGATCGAGACCATCCTGACCAACATGATGAAACCCCAACTCTACTAAAAAGACAAAAATTAGC 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_001144900.3 |
Synonyms | COXPD49; MID49; SMCR7 |
Summary | This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011] |
Locus ID | 125170 |
MW | 70 |
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