WBSCR22 Protein (His tag)
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- 抗原 See all WBSCR22 蛋白
- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
- 蛋白类型
- Recombinant
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宿主
- 人
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资源
- 大肠杆菌(E. Coli)
- 标记
- This WBSCR22 protein is labelled with His tag.
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
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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
- 纯度
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product WBSCR22 蛋白
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- 应用备注
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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 - 说明
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The tag is located at the N-terminal.
- 限制
- 仅限研究用
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- 浓度
- 50 μg/mL
- 缓冲液
- 25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
- 储存条件
- -80 °C
- 储存方法
- 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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- 抗原
- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
- 别名
- Wbscr22 (WBSCR22 产品)
- 别名
- 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
- 背景
- 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.
- 分子量
- 31.7 kDa
- NCBI登录号
- NP_059998
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