MSF (SEPT9) (NM_001113493) Human 3' UTR Clone
CAT#: SC217183
3`UTR clone of septin 9 (SEPT9) transcript variant 2 for miRNA target validation
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Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | SEPT9 |
Synonyms | AF17q25; MSF; MSF1; NAPB; PNUTL4; SEPT9; SeptD1; SINT1 |
ACCN | NM_001113493 |
Insert Size | 1979 |
Sequence Data |
>SC217183 3'UTR clone of NM_001113493
The sequence shown below is from the reference sequence of NM_001113493. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC CAACGGCATGGAGGAGAAGGAGCCAGAAGCCCCGGAGATGTAGACGCCACCCTGCCCACCCCCGGGATCC TGCCCCCAAGTCATTTCCGTCCCCCCCCAGGCCCTCCCACCACCCCATTTTATTTTATATGATTTTCTCC ATTTGTCATCGTTCCCCACCCCTTCGACATGCTGCCAGGAAACAAGGGAAGGGGCCTCCCTCCGAGTGAG TCAGTGATGAGGCCGCGGCCTCCCCGAGGTTGTGGGGAGGCTGCACTGGAGCCACAGGCAGGGGTGAGAG CACCCACTGAATTGACATGACCCTCTGTCCCCAGGCCTGGCTCCCCGAGGGCTCAGAAGAGCAGCTTCGG TGTGCAGATCATCCGTCTGTGTGGGGTTCTCAGTGCCGGAGGCCTTGGGGTGGGGGCCAGGCCTCGCACT TGCAGAGGAGCCCAGTGGGCTGCACGCTCCCCTCCATCCCCATCGGCCCTGTCCCCTGGAGTGTGTCAGA GCCCAGGGGAGAATGCAGCCCACCAGGAGCACCTGGACCCCCTGCCCGCCACATGGTGTGGCCATCACTC AGCCCCTACCCCTGCCCTGCTCCTAAGGGTAGAAAACTCCAGGGTCCCCTGCCACCGACTGCCCAGCCAC TCCAAGCCCCCTGGCAGCTGCCCCTCCTGGAGCAGAAAGTGCCTTTATCTCAGCCATCCGCAGACTGCTT GGCCAGATGCGGGGACAGGCTGGAATGAGGGAGGCGTCTTCATCTCCCTGCCATCCCCCTCTCACGCCAC CCCCGCCCCCACCGGGCTGCAGGTGCTGCTGATGCGCTGGGATCTGATTGAGGATAAAAAGGAAGGAGAG ATGACCCCTACCCCCTCATCCCCCAGTTTTGAAAAGGTCTAAGCAAGTGAGTCTGGTGGAGGAGCTGAGG GAGGGAGCCATGGAAGGTGCCAGAAGGAAGGTTGGCGGGGGCACGTGTGGGCCGTGGCTTGGGCTGGTCA GAGTGGCGTGAGCTGCCCGGCGCCTGCCCTGCCCAAGTGACCAGGGAAGTGTGTGTGTGTCCATGTGTAT GCGTGTCCGTCTGTCTGTCTAGTGTCTGGGTTTGGCCCAAGACTGGGCTGTAGTTACATTAATGCCCAGC CAGCCACCCCTGCCACTCACCCCTCCTGGCCCAGGCCTTGCTGACTCTCTGAGCTGGGGAGGTGGGAGGC CAGGCGAGCCTGACTCTGTTGATCTACCCGTGCCTGGGCCCCTCCCCTCAGAGCCCATGGTAACGAACCC CTAGAAAGGAGAGAACGGGCGTCAGGGGTGCACAGTCCACAGCTGAAGAGCAAGGTTTCGTGGCAGCACG GCCCGGCCCCTCACCCTCTGTCCCCACGAGGGGACCCATGGGGGCTGTCTTTGCAGGGCACAGATGACCA AAGTCCCTTCCTGCTTCCTGTTACCTGTCTTGCTCCTGGGGAGAAAGAGGGGCCTGATGAGACTCCACTC AGGTGCACACATCACCAGGTGCATCTGCAGGCACCGGGCTGGCTGCTTGCAGCCAGGAGAAGGTCAGCGA GAAGGAGTGTATGAGTGTGAGTGTGTGTGCATGGAAGTTGGGGCACTGGGCGTCTGACTCCCTCCCCACC CAAGAGAGGAAGGACCCCTCACCACCCCCACTGGCGAGACAGTTTACTTTGCCGACTTGCCATGTTTTTG CCAAAACCAAGATTTTGAAGGAAATGAGTGGCCAGCGCCAGGGCCCAGGCCATGTGGCCTGCCCAGCCTC AATGTCACTTGGTGGCGGGGTGGGGTGGGGGTGGGCAGCAGCATCCCAGCCTTGAGATGCTTCACTTTCC TTCTCTGTAACCAGACTTTGAAAAATTGTTCGTTTCATCAGGCTCTGTTCCTCAATGGCCTTTTGCTACG TGCCTCCCGAGAAATTTGTCTTTTTGTATAAATGACAAAGTGTTGAAAATGTATTTCCTGAAATAAATGT TTCAAATGCAGAAACCCAG ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
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_001113493.1 |
Summary | This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2009] |
Locus ID | 10801 |
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