PROX1 (NM_002763) Human 3' UTR Clone
CAT#: SC207956
3' UTR clone of prospero homeobox 1 (PROX1) for miRNA target validation
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CNY 5,464.00
货期*
现货
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | PROX1 (NM_002763) Human 3' UTR Clone |
Vector | pMirTarget |
ACCN | NM_002763 |
Insert Size | 587 bp |
Sequence Data |
>SC207956 3' UTR clone of NM_002763
The sequence shown below is from the reference sequence of NM_002763. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC GAACTGCCTACAAGAGCTGCTTCATGAGTAGAAATTTCAACAACTCTTTTTGAATGTATGAAGAGTAGCA GTCCCCTTTGGATGTCCAAGTTATATGTGTCTAGATTTTGATTTCATATATATGTGTATGGGAGGCATGG ATATGTTATGAAATCAGCTGGTAATTCCTCCTCATCACGTTTCTCTCATTTTCTTTTGTTTTCCATTGCA AGGGGATGGTTGTTTTCTTTCTGCCTTTAGTTTGCTTTTGCCCAAGGCCCTTAACATTTGGACACTTAAA ATAGGGTTAATTTTCAGGGAAAAAGAATGTTGGCGTGTGTAAAGTCTCTATTAGCAATGAAGGGAATTTG TTAACGATGCATCCACTTGATTGATGACTTATTGCAAATGGCGGTTGGCTGAGGAAAACCCATGACACAG CACAACTCTACAGACAGTGATGTGTCTCTTGTTTCTACTGCTAAGAAGGTCTGAAAATTTAATGAAACCA CTTCATACATTTAAGTATTTTGTTTGGTTTGAACTCAATCAGTAGCTTTTCCTTACATGTTTAAAAATAA TTCCAATGACAGATGAGCAGCTCACTT 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_002763.3 |
Summary | The protein encoded by this gene is a member of the homeobox transcription factor family. Members of this family contain a homeobox domain that consists of a 60-amino acid helix-turn-helix structure that binds DNA and RNA. The protein encoded by this gene is conserved across vertebrates and may play an essential role during development. Altered levels of this protein have been reported in cancers of different organs, such as colon, brain, blood, breast, pancreas, liver and esophagus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012] |
Locus ID | 5629 |
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