SMCR7 (MIEF2) (NM_148886) Human 3' UTR Clone

CAT#: SC211971

3' UTR clone of Smith-Magenis syndrome chromosome region candidate 7 (SMCR7) transcript variant 2 for miRNA target validation



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CNY 4845.00


货期*
3周

规格
    • 10 ug

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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_148886) Human 3' UTR Clone
Vector pMirTarget
Synonyms COXPD49; MID49; SMCR7
ACCN NM_148886
Insert Size 1818 bp
Sequence Data
>SC211971 3’UTR clone of NM_148886
The sequence shown below is from the reference sequence of NM_148886. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
GGCCTACAGGAGCCCGAGGGGCTGCTCTAGGTGGGTGGAAACGGGTGGTTGCCATGTTTTCTAATGCTG
GGGAGCTGCACCCACCTCCCTTCCAGGGATTTGAATAGTGGTTTTTCTCTAGCTTTTTGCCAGAACAAA
GGAGGGTACATTACTTAAACCCAGGGCATCAGGATGTGCTTGGGCTATGGTGGCCATAAACCCTGAGCC
CAGAGAGCTTGGGTCACTGTCACCTGAGTGCAGCTGGGCTGCCTCAGGCAGCTTGGAGTGCCAGCCATT
CCTGCAAGCACCGTTTCAGCTCTTGGGGCCAACCCCAGGACCTTTGGCTCTGTCCATCACCAGCAACCA
ATCCACCAACAGAATGTGGTTTCTGCCATCCTGGGCAGAAGCTGAAGGCCAGCTTCACATTTCTGCTGA
GAGAAGGTGACTTAACGCCTTTTCCGGCCCTAGCTCCAGGCGTTTTGAGGCGTCTGGTGCCTGATGGTA
GGTATGGTGTGTTTGTTCTGTCCCCCAGGGGCTGGAGTCACCTGGTGCCCCTGAAGGACAGATTTTTGG
CTGTTAAAGGATGGCATTTTCCTGCTGTCTTCTGTGCGTTTAGTTTTCTTGCTGAGCGGGAGCTCAGTA
TGACTTGCCACCCACCTGATACCTCAGGGCAAGGCCCTTTTTCCCTCCAGCCAGGTGAGTGTTTTCTTC
AGGCAGCTGAGGGTCCTGGGGGAGCTGAGGCTCTGTGCTGCACCCCCAGCCCACAGCTGGGGCATCTCA
CTGGAGCTGTTCCAGGCCCCACTGGAGAGCAGAGGACCTGATCCCCCACTAGAGAGGTCCGGTGTGCAC
AGCCGGCCTCCCAGTGTGCCAAAATGAACTGCTCTCAGCTGATGGCTGTATTCTGACTTTGAAGCCTGT
TAAGAGGTAGCAAGGGGGCTAGAGGAGGGAGATTCCACCTCCCCTCCCAAGTGACCCTCCTCCTGCCTC
TGGTATCCTTCCTTTTGAAACGAAGCTCAGCTTCGAAGATGTGAACAAGAATAAAAGGAAAAAATTCTA
ATGTATATATAACTCAGGCTGGATAAGGGAGTCTTGGTGCTTTCATACGCAGCTGTTGAGGGTTTTCTG
TAAGTCCTGTGGCTTGTCCTGGCACTTTGGCAAGAGTGCTTGAGGTCAATTGGAGGTGGTAGAGTTTAC
TTTAAAAAGTAGCATCTTGGCCGGGTGTGGTGGCTCGCATCTGTAATCCCAGCACATCGGGAGGCCGAG
GCGGGCGGATCACGAGGTCAAGAGATCGAGACCATCCTGACCAACATGATGAAACCCCAACTCTACTAA
AAAGACAAAAATTAGCTGGGCGTGGTGGCACGCACCTATAGTCCCAGCTACTCGGGAGGCCGAGGCAGG
AGAATTGCTTGAACCCGGGAGGTAGAGGTTGCAATGAGCTGAAATTGCACCACTGCACTCCAGACTGGC
GACAGAGCAAGACTCTGTCTCAAAAAAATAAATAAATAAGCATCTTGGCCCCGCGCTGTGGCTCACGCC
TATAATCCCAGCACTTTGGGAAGCCGAGGCCGGTAGATCACCTGAGGTTGGGAATTCAAGACCAGGCTG
ACCAACGTGGAGAAACTCCATCTCTGGTAAAAATTCAAAAAAATTAGCTGGGCATGGTGGCACATGCCT
GTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCGGAGGTTGTGGTGA
GCTGAGATCGTGCCAGTGCACTCCAGCCTAGGCAACAAGAGTGAAACTCTGTCTCAAAATAAAATAAAA
TAAAATAATAATAGTAATAATAAA
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_148886.2
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 67.5
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