WBSCR22 Protein (His tag)
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- Antigène Voir toutes WBSCR22 Protéines
- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
- Type de proteíne
- Recombinant
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Origine
- Humain
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Source
- Escherichia coli (E. coli)
- Purification/Conjugué
- Cette WBSCR22 protéine est marqué à la His tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human WBSCR22 (full length, N-term HIS tag, transcript variant 2) protein expressed in E.coli.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product WBSCR22 Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the N-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
- Stock
- -80 °C
- Stockage commentaire
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Antigène
- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
- Autre désignation
- Wbscr22 (WBSCR22 Produits)
- Synonymes
- MGC82375 Protein, wbmt Protein, pp3381 Protein, hussy-3 Protein, hasj4442 Protein, zgc:162306 Protein, HASJ4442 Protein, HUSSY-3 Protein, MERM1 Protein, PP3381 Protein, WBMT Protein, 1110003N24Rik Protein, Williams-Beuren syndrome chromosome region 22 Protein, BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog Protein, BUD23, rRNA methyltransferase and ribosome maturation factor Protein, williams Beuren syndrome chromosome region 22 Protein, hypothetical protein Protein, WBSCR22 Protein, bud23.L Protein, bud23 Protein, CpipJ_CPIJ001394 Protein, PAAG_00857 Protein, MCYG_07273 Protein, PGTG_07527 Protein, PGTG_12505 Protein, BUD23 Protein, Bud23 Protein
- Sujet
- 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.
- Poids moléculaire
- 31.7 kDa
- NCBI Accession
- NP_059998
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