![ERAB (HSD17B10) Mouse Monoclonal Antibody [Clone ID: LBI10B4]](https://img1.dxycdn.com/2022/0707/344/1496323853485278553-14.jpg)
- ￥690 - 2025
- Leading Biology
- AMM09341V
- 美国
- 2025年07月13日
- WB 1:1000, IHC 1:50, IF 1:100, Flow 1:100
- Mouse
- Human, Mouse, Rat
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- 详细信息
- 技术资料
- 靶点：
HSD17B10
- 浓度：
1 mg/ml
- 应用范围：
WB 1:1000, IHC 1:50, IF 1:100, Flow 1:100
- 宿主：
Mouse
- 适应物种：
Human, Mouse, Rat
- 保质期：
1-2年
- 供应商：
安诺伦（北京）生物科技有限公司
- 标记物：
Unconjugated
- 克隆性：
Monoclonal Antibody
- 保存条件：
Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
- 形态：
PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
- 亚型：
IgG1
- 免疫原：
Full length human recombinant protein of human HSD17B10(NP_004484) produced in HEK293T cell.
- 规格：
100 ul/30 ul
| 规格： | 100 ul | 产品价格： | ￥2025.0 |
|---|---|---|---|
| 规格： | 30 ul | 产品价格： | ￥690.0 |
别名：17b-HSD10; ABAD; CAMR; DUPXp11.22; ERAB; HADH2; HCD2; MHBD; MRPP2; MRX17; MRX31; MRXS10; SCHAD
产品概述：Anti-HSD17B10 mouse monoclonal antibody, clone LBI10B4
总结：This gene encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids, alcohols, and steroids. The protein has been implicated in the development of Alzheimer's disease, and mutations in the gene are the cause of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (MHBD). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined.
产品概述：Anti-HSD17B10 mouse monoclonal antibody, clone LBI10B4
总结：This gene encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids, alcohols, and steroids. The protein has been implicated in the development of Alzheimer's disease, and mutations in the gene are the cause of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (MHBD). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined.
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ERAB (HSD17B10) Mouse Monoclonal Antibody [Clone ID: LBI10B4]
￥690 - 2025
