BUD23 (NM_017528) Human 3' UTR Clone
CAT#: SC204759
3' UTR clone of Williams Beuren syndrome chromosome region 22 (WBSCR22) for miRNA target validation
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CNY 4845.00
货期*
                        3周
                    规格
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                Specifications
| Product Data | |
| Product Name | BUD23 (NM_017528) Human 3' UTR Clone | 
| Vector | pMirTarget | 
| Synonyms | HASJ4442; HUSSY-3; MERM1; PP3381; WBMT; WBSCR22 | 
| ACCN | NM_017528 | 
| Insert Size | 356 bp | 
| Sequence Data | >SC204759 3’UTR clone of NM_017528  The sequence shown below is from the reference sequence of NM_017528. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACCGGCCGCAAGCGCAAGCCCCGCTTCTAAGTCACCACGCGGTTCTGGAAAGGCACTTGCCTCTGCACT TTTCTATATTGTTCAGCTGACAAAGTAGTATTTTAGAAAAGTTCTAAAGTTATAAAAATGTTTTCTGCA GTAAAAAAAAAGTTCTCTGGGCCGGGCGTGGTGGCTCACACCTGTAATCCCAGCACCTTGGGAGGCTGA GGTGGGAGGATCATTTGAGGCCAGGAGTTTGAGACCTGCCTGGGCAACATAATGAAACTTCCTTTCCAG GGAGGAAAAAAAAAAAAAAAAAAAGCTCTGAGAGCATCTTATTTTGTTTAAAGGCAAGAAATAAAATTT CCTTTTGTGGA 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_017528.5 | 
| Synonyms | HASJ4442; HUSSY-3; MERM1; PP3381; WBMT; WBSCR22 | 
| Summary | This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011] | 
| Locus ID | 114049 | 
| MW | 13.3 | 
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