AP2 alpha (TFAP2A) (NM_003220) Human 3' UTR Clone
CAT#: SC216216
3' UTR clone of transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha) (TFAP2A) transcript variant 1 for miRNA target validation
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CNY 5795.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | AP2 alpha (TFAP2A) (NM_003220) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | AP-2; AP-2alpha; AP2TF; BOFS; TFAP2 |
ACCN | NM_003220 |
Insert Size | 1770 bp |
Sequence Data |
>SC216216 3’UTR clone of NM_003220
The sequence shown below is from the reference sequence of NM_003220. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGTGACAAAGAGGAGAAGCACAGAAAGTGAGGCTCTCCTCCCGCCCCGCCCCTCCCACGCCTCACCAGC CCCCCGCGCGCCCACCCTCCGGCGGGTGACAGCTCCGGGATCAGCAACCCTTCCTGCTGCTGCTACTGC TGCTGCTGCTGCCGCCGCCGCCGCCGCCGCTGCCCTTGGGTCCCCCCGAGTCTCCGGGACTGCCCTCTC GACTGTCAGTGGGGCAGCCTCTCCGACTCTGCACCCGCCTCGACCTCCCCACCCGCTCCCACACCCCTG TGCCCTCATGTGGAGCCTAAGAGAACAGAACAGGCCGTGAAGCCAGCAGAGAAAAGTTCTGCCAAGTTT GTGAACCCTTTTTTTTTTAAACAAAACAACAAATCAACAACAGCAACAACAACAACAAAAATTAAAAAC TTTTTTCTAAAAAAAAAGTGAAAATAAAAAAAATTATATGCGCTTCATGGGACTGAGTCACCACCTTCC CTTACATACTTCAGTTCAGATTGTAGCCATACTTAAAAAAAAAAAAAAAGCCAAAAGATGATGACAACA TTTTTATCAGTATTGTGAATAAACTTGAACACAAATACACGAAGTTCCATGTCATGTCTTCAGTTGTAG AAGTTTTTCCTCTTTAAGGTAAAGCGACCAACTTGAACTTTCTCTGGCAACACGATTCGCAGTTATATA AGGGAATCAGTGTTCACGTCTCTGTATATATTTATTTATGTGTAATTTAATGGGAATTGTAAATATGGT GAGTCTGTTTTAAGCCTTTTTTTTTTTATTTATCTGATCTTGTTTACCTCTTGTTTAGTGGGTTTTGAA TCTTCCCTATTAGTTCTTCATGTGGTTCATGGTACTGATTTAGAAATCCAGTGTTTGGGGGATTTTTTT CTCTGGGATTCATGAATTTAGCCCTGTTGTAGCATGTTAAAGGTGACAAACAGCTGGACAAATTTTTAA AAAGTAAAATAAAATTTTATCTATAATTAGTATTATTACATTTAGCTTTTCATTGAACCGAAAGAAAAA AAGTGATATTGGACCCTGGAAAGATTTTGAAACTTGAGTGGTTTGATAACCCTTCTATGTATTGTAGGG AGAAAAAAAAAAGTTTATTTTATTCCACTGTCCTCCCTTAAAAGCATCATTTGAGCAATAAATGAATAT TGTCTTTAAACCAAGGGTTAGGGAATTTTCCTCTCTCTCTCTCTCTCCTCTCTCTTTCTGTTCAAAGAA CTTCAAACATTTGGGACCACCTGGTATTCTGTATTTTCACTGGCCATATTGGAAGCAGTTCTAGTTGCA TTGTATTGAGTTGTGCTGGCAGTAGTTTCCATGCCTGTCAATGTATCATAGTCCTTTGTTGCCCAGATA AATAAATATTTGATACGCTTTATGTCGATTTTTTTTTATTCAGTGGCTGTCTTTACCCAGGCGTATTTT TGTTCTTGGCAGTATTTTTTATTCAGTATGGTTACAGTAATTGAGTTTAACTCTCCCTTGGCAATTGCT CCTTGCAATAAGCAGCTGAACCCATTGTTTCCCTCAAGTATAATAAAAACTTACTTTCAACTTGGAGTT CAGAGCAGGGTATCATTTAGATATTCCACTGTGTCTGTATTCAGACAAATGACACAATAAAACCCAATG TATTCTTTTGGATAAAAGATTGTTTGTACTGCTAAAGGAATGACATACTGTCTTTTCCTTACTAGAAAC ATTAATTTTATTATTAAAAATAAAGTTTTATTTTATTTATGTTGA 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_003220.3 |
Synonyms | AP-2; AP-2alpha; AP2TF; BOFS; TFAP2 |
Summary | The protein encoded by this gene is a transcription factor that binds the consensus sequence 5'-GCCNNNGGC-3'. The encoded protein functions as either a homodimer or as a heterodimer with similar family members. This protein activates the transcription of some genes while inhibiting the transcription of others. Defects in this gene are a cause of branchiooculofacial syndrome (BOFS). Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009] |
Locus ID | 7020 |
MW | 67.3 |
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