Order NO. D621972
人BCAP31抗原（重组蛋白）
| 英文名 | Human BCAP31 Antigen (Recombinant Protein) | ||
| 别名 | CDM; BAP31; 6C6-AG; DXS1357E | ||
| 相关类别 | 抗原 | 储存 | 冷冻（-20℃） |
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| 编 号 | 包装 | 库存 | 目录价（￥） | 您的价格（￥） | 数 量 |
| D621972-0001 | 1 MG | 预计30日内发货 |
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| D621972-0100 | 100 UG | 预计30日内发货 |
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产品描述
概述
Fusion protein corresponding to a region derived from 124-246 amino acids of human BCAP31
属性
| Full name: | B cell receptor associated protein 31 |
| Synonyms: | CDM; DDCH; BAP31; 6C6-AG; DELXQ28; DXS1357E; MICRODELXq28 |
| Swissprot: | P51572 |
| Gene Accession: | BC014323 |
| Gene ID: | 10134 |
| Purity: | >85%, as determined by Coomassie blue stained SDS-PAGE |
| Expression system: | Escherichia coli |
| Tags: | His tag C-Terminus, GST tag N-Terminus |
| Research areas: | Cancer |
| Reconstitution: | Reconstitute with sterile distilled water or deionized water to 1 mg/ml |
| Background: | This gene encodes a member of the B-cell receptor associated protein 31 superfamily. The encoded protein is a multi-pass transmembrane protein of the endoplasmic reticulum that is involved in the anterograde transport of membrane proteins from the endoplasmic reticulum to the Golgi and in caspase 8-mediated apoptosis. Microdeletions in this gene are associated with contiguous ABCD1/DXS1375E deletion syndrome (CADDS), a neonatal disorder. Alternative splicing of this gene results in multiple transcript variants. Two related pseudogenes have been identified on chromosome 16. [provided by RefSeq, Jan 2012] (The background information is obtained from official databases and does not represent the product information.) |
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