Order NO. D621771
人ACSL4抗原（重组蛋白）
| 英文名 | Human ACSL4 Antigen (Recombinant Protein) | ||
| 别名 | ACS4; FACL4; LACS4; MRX63; MRX68 | ||
| 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 |
| D621771-0001 | 1 MG | 预计30日内发货 |
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| D621771-0100 | 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 462-711 amino acids of human ACSL4
属性
| Full name: | acyl-CoA synthetase long chain family member 4 |
| Synonyms: | ACS4; FACL4; LACS4; MRX63; MRX68; XLID63 |
| Swissprot: | O60488 |
| Gene Accession: | BC034959 |
| Gene ID: | 2182 |
| 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: | Metabolism, Signal Transduction |
| Reconstitution: | Reconstitute with sterile distilled water or deionized water to 1 mg/ml |
| Background: | The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the cognitive disability or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants. [provided by RefSeq, Jan 2016] (The background information is obtained from official databases and does not represent the product information.) |
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