BUD23 (NM_017528) Human Recombinant Protein
CAT#: TP760856
Purified recombinant protein of Human Williams Beuren syndrome chromosome region 22 (WBSCR22), transcript variant 2, full length, with N-terminal HIS tag, expressed in E. coli, 50ug
Frequently bought together (1)
Rabbit Polyclonal antibody to WBSCR22 (Williams Beuren syndrome chromosome region 22)
USD 625.00
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Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding human full-length WBSCR22
|
Tag | N-His |
Predicted MW | 31.7 kDa |
Concentration | >0.05 µg/µL as determined by microplate BCA method |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 25 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% sarkosyl, 10% glycerol |
Note | For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process. |
Storage | Store at -80°C. |
Stability | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Reference Data | |
RefSeq | NP_059998 |
Locus ID | 114049 |
UniProt ID | O43709, C9K060 |
Cytogenetics | 7q11.23 |
Refseq Size | 1256 |
Refseq ORF | 843 |
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] |
Protein Families | Druggable Genome |
Protein Pathways | Androgen and estrogen metabolism, Histidine metabolism, Selenoamino acid metabolism, Tyrosine metabolism |
Documents
FAQs |
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Resources
Recombinant Protein Resources |
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