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
    • 10 ug

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Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1280.00

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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