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 4,845.00


货期*
3周

规格
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00

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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