OTX2 (NM_021728) Human 3' UTR Clone
CAT#: SC212018
3' UTR clone of orthodenticle homeobox 2 (OTX2) transcript variant 1 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | OTX2 (NM_021728) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CPHD6; MCOPS5 |
ACCN | NM_021728 |
Insert Size | 1860 bp |
Sequence Data |
>SC212018 3’UTR clone of NM_021728
The sequence shown below is from the reference sequence of NM_021728. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACATCCTCGTGGAAATTCCAGGTTTTGTGAAGACCTGTAGAACCTCTTTTTGTGGGTGATTTTTAAATA TACTGGGCTGGACATTCCAGTTTTAGCCAGGCATTGGTTAAAAGAGTTAGATGGGATGATGCTCAGACT CATCTGATCAAAGTTCCGAGAGGCATAGAAGGAAAAACGAAGGGCCTTAGAGGGGCCTACAAACCAGCA ACATGAAATGGACAAACCAATCTGCTTAAGATCCTGTCATAGTTTTAGATCATTGGTTATCCTGATTTG CAAAGTGATCAAAAGCATTCTAGCCATGTGCAACCAAACACCACCAAAAATAAAATCAAACAAAACTAA GTTGTGAAGGAAGGGAGGGAAGGTCATAGCCTTCTTAAGCAGAGGTGTTCCATTGTTTTAGCCAATCCT TGGTTGAATCTTAGGAATGAACAGTGTCTCAAGCTCATTCACGTTTCATGACCAACTGGTAGTTGGCAC TGAAAAAACTTTTCAGGGCTGTGTGAATTGTGTGACTGATTGTCCTAGATGCACTACTTTATTTAAAAA ATAATGTTCATAAGGAGTCAATATGTAGTTTAAGAGACAATCAGTGTGTGTCTTATAAATGGTACATCT GTGGTTTTTAATCTGTGCTAGACTTCAAAACTGTGATCTCCTGTTATTGTATGCAACCTTGAACTCCAC CTCTGCAGGGGTTCTTCTGTGATTAAATAGGTTATAATTATAAGCAAAATTCAGAGCAACTGAGTACTG ATCTAAAAAGATTACCTTTGGCTGGAGGTGAGCTGCACTGAAACTTTACGACAAAATGTCTCTGGACAA AGAGAGTCAGAGAAGAGAAGCAAAAGGACACTAATTCATCTGTAATTTACTGTTGGTAAGCCTAGCAGT AAAGAGACATTGGTCAATTGCTCTGACCCTGATGAATTATTAAACTGAGATCATTGTCGTTTATGCTTG CAGATGTTAAATGGAAAAGTTATATATGCATAAACCTTTTCTTCCTGGATTTGGCAGATATGTATAATT ATATTAAAATGGTTCTAGCACAACATTGGGTCCAGTTTAATTTTACACCGCTATTTATGAATAAGAAGC CTACATTCAGCCTTTCCTCCCCAAAACACGTTTTTCTTAGGACAGAGAGTAAATTAGCAAACTTATTTT TACTTTTTTTTTTTGCTAATCTATGCATAAAATAGATATGAATGACAGTGGTAGGTAGACTTTTTGTGA CTTTCATCAGGATTGCTCTGAAATTGAGTTTGGAGAGCCTAACAACAAGATCTTGTTTTCCTTGCTTTT CCCTCCCTACTTCAAACCTGAACGATTTCTTAGGCACTTTATTAGAATGTTTTAAAATATATCAAGTTT TTAAGAGGGAGGAGGAGAATTGGAGTATCTCTGAAAACATGAGAATGACAAGAATTTCTTGTTACTATT CTCTTATTTGATTAAGGGGATTTTTTTTTTTTAACTTCCAAAAACTGAGGTAAACATGAGAGGGAGTGT AATCAGAATCTGAAAGTAATTCAGGCAGAAATGATTCCTGAACAAAAGAGTTTCAGAAAAGTTTTAAAA CCTATAATTTCAGTAGTTGAACATAAGGCACCCTGGTCAGTTTGTGTGTATGTGTTTAAGAAAGTGCCG AGGGGGAAAAAATGGGTCCCTTTTCAGTTGTACCTGCATTTTGTAAACCAGTCACCAGAAAAGACAAAT GGGCCAATGATCATGGTGCTCCTCAGGTAAAAGCAATATTTAATTTCATTTTAAGCTGCTTAAGCTCTT ACAGCTGACCAAAATTAAGTGACTCTTGATTGTAACGTTTTAAATGAAGGTTAGCAGTTGCAACCA 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_021728.4 |
Synonyms | CPHD6; MCOPS5 |
Summary | This gene encodes a member of the bicoid subfamily of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and plays a role in brain, craniofacial, and sensory organ development. The encoded protein also influences the proliferation and differentiation of dopaminergic neuronal progenitor cells during mitosis. Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone deficiency 6 (CPHD6). This gene is also suspected of having an oncogenic role in medulloblastoma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Pseudogenes of this gene are known to exist on chromosomes two and nine. [provided by RefSeq, Jul 2012] |
Locus ID | 5015 |
MW | 71.6 |
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