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C19orf61 (SMG9) (NM_019108) Human 3' UTR Clone

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SKU
SC206278
3' UTR clone of chromosome 19 open reading frame 61 (C19orf61) for miRNA target validation
  $683.00
4 Weeks*
Size
Bulk Requests & Clone Modifications

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Specifications
Specifications
Product Data
Vector pMirTarget
Species Human
Transfection Reporter RFP
Assay Reporter Luciferase
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Target Symbol C19orf61
Synonyms C19orf61; F17127_1; HBMS
ACCN NM_019108
Insert Size 2000 bp
Sequence Data
Insert Sequence
>SC206278 3’UTR clone of NM_019108
The sequence shown below is from the reference sequence of NM_019108. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
CTGGCAGAGTACAGCCGCCTGCTGGCCTGAGGCCAAGGAGAGGAATGTCATGCAGGGGACCTCCTGGGT
CCGCAGTGTACTGCGAGGGAGCACAGATGTCCATCCCCCGCTGGGGTGGAGAGCGGCAGCAGGCCTGAT
GGATGAGGGATCGTGGCTTCCCGGCCCAGAGACATGAGGTGTCCAGGGCCAGGCCCCCCACCCTCAGTT
GGGGCTGTTCCGGGGGTGACTGTGAGCGATCCCACCCCAAACCTGAGATGGGGTAGCCCGTCCTGTGTC
CTCCACAGGGACAAGCAGTGGGAGGAGTCTGAATGGTCACCAGGAAGCCCGGGCTCCATCTTGACCTCC
TTTTTCAGGGACAGGAGCAACAGGCCCCTCTTCCCTGACTCTAAGCCCTTCCCTGTAAGGTGAGGCAGG
GTCTGGAGAGCTCTTTATTGGAACAGATCTGGTGGTTCAAATAAACACAGTCATGCAAGCCTGTTCTTA
TGTTCCACTTACTCCTCTACCCACCATGCAGCTCTGGGAAGCAGGACAAATTGGACACCCAGCCCTTGC
GGGCAGATGGAGATCAGTCTCTGCTAAGAAGTCCCTAGAAGGGGTTATTCTGTTTCCTGGGGTGGCATC
AAGCCTCCCCTGTGTATGTTTTGGATGGGAAAATACACTGGTGCAGCTGAGTACAGCAACTACCCTCGT
GTCTTCTGCTCTCACTTAAAGACAGTTACCTGCCTTTGGGTTAAATGCCCAGTTAAATACAGTGCCTAG
GCTGGGCATGGTGGCTCACGTCTATAATCCTAGCACTTTGGGAGGCCGAGGCAGGCGGATCACTTGAGA
TCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAGACCCTGTCTCTACTAAAAATACAAAAAAAAATT
AGCTGGGCGTGGTGGCGCACGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGTGGGAGAACTGCTTGAA
CCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCTCCAGCTTGGGCAACAGAGCGA
GACTCCGTCTCAAAAAAAAAAAAAAAGCCTACTTTTGACTTAAGAAACAGAACTTGTCCTTAAATGTAG
TAAGTACTTACCCTTAATCCAAATACCATGCCTCACCCGTACAGACAGTGCCTTCTGTTGGTTAAATAC
AGTGGCTTTCCTCTCGTAAACCTCATCTACTCTTGCTTAGAAATGGCAACCCTCACCTTTAATGTAAAT
CCAGAACCTACCCTCAGTTAAATCCACTCTGCGATTTGGTACAGTACCAACCCTCATCTGCTCAGTTAA
ATACAGTACATGATCTTAGTTTGAGGTTTCCCAAAGTATGTCTCCAAATTGGTCTCGCCACCCCAAATT
AATCCATCGTTCAGTAAAGCAGTCAGCTCCAGTCCAGCTGGCTGAGTCTGTTCATCCATTGCCCTCCCC
CACCCCCTGCCGCCCGTGGCACATATTTGTCTCCCTGGTTTCCTCCTGCTTTCAAGCATCCCATACAGC
CCTGGTGTTTCATACCATGGGGATCCAGGGCCTTGTGAGAAACAACTGAAGTGAGGGGGGGCGGGGGGT
CAGTGAAGAAAGCACTCAGCAGGGCCAGAGAAGGTCAGGCCAGAAGTGGATAGAATGCCAGTCTCTACA
GAGGGCTGAGGCCTGGGAGACAGGAGGCCCAGCACAGGCTCTGGCACAGCCACTTCCTGACCGACTGTA
GTAGGCAAGGAGCCTCCCCTCTCTGGCCATTATTCCAACATTTAAGATCATCCTCGAGGCCCTTCAGAG
CTGTGACATTCACTGCCCTTTTACCGAAATGCTTCTAAATCCTTTGCCCCACTGTCGTGATCTCTACAG
AACCCTCCTGACCATCCTCTCCAGCTAGATAACCCAGCTCTTCCCTGCCTTGTCAAAATGTCTGCCCCA
AGTCTCATCCCCACCCCTGCTTCCCCAGGGGGTCTTCCTGCTGGTTGATTTGGGGGTTTGCCAGAGTA
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).
Components The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials.
Note Plasmids are not sterile.  For experiments where strict sterility is required, filtration with 0.22um filter is required.
Shipping Ambient
Reference Data
RefSeq NM_019108.4
Locus ID 56006
Summary This gene encodes a regulatory subunit of the SMG1 complex, which plays a critical role in nonsense-mediated mRNA decay (NMD). Binding of the encoded protein to the SMG1 complex kinase scaffold protein results in the inhibition of its kinase activity. Mutations in this gene cause a multiple congenital anomaly syndrome in human patients, characterized by brain malformation, congenital heart disease and other features. provided by RefSeq, Jul 2016
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