17beta-HSD4 (N-Term) 抗体
The 兔 多克隆 anti-17beta-HSD4 antibody (ABIN7218302) specifically detects 17beta-HSD4 in WB, ELISA, IF 和 IHC.
The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN7218302
发货至:
中国
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中国
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北京 101111
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Quick Overview for 17beta-HSD4 (N-Term) 抗体 (ABIN7218302)
抗原
17beta-HSD4
适用
人, 小鼠, 大鼠
宿主
兔
克隆类型
多克隆
标记
非结合性
应用范围
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (IHC)
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抗原表位
- N-Term
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原理
- Rabbit Anti-17β-HSD4 Polyclonal Antibody
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特异性
- 17β-HSD4 Polyclonal Antibody detects endogenous levels of 17β-HSD4 protein.
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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免疫原
- Synthesized peptide derived from the N-terminal region of human 17beta-HSD4
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亚型
- IgG
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anti-17beta-HSD4 (N-Term) antibody
适用: 人, 小鼠, 大鼠 WB, ELISA, IHC (p) 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,IHC: 1:100-1:300,ELISA 1:20000,IF 1:50-200
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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有效期
- 12 months
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- 17beta-HSD4
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背景
- HSD17B4, EDH17B4, Peroxisomal multifunctional enzyme type 2, MFE-2, 17-beta-hydroxysteroid dehydrogenase 4, 17-beta-HSD 4, D-bifunctional protein, DBP, Multifunctional protein 2, MPF-2Peroxisomal multifunctional enzyme type 2 encoded by HSD17B4 is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
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分子量
- 80kD
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基因ID
- 3295
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UniProt
- P51659
抗原
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