HSD17B4 抗体
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北京 101111
Quick Overview for HSD17B4 抗体 (ABIN7241504)
抗原
See all HSD17B4 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Recombinant protein of human HSD17B4
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亚型
- IgG
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anti-Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4) antibody
HSD17B4 适用: 人 WB, IHC (p), IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4) (N-Term) antibodyHSD17B4 适用: 人 WB, IHC (p), IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4) (AA 437-736) antibodyHSD17B4 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4) (AA 510-736) antibodyHSD17B4 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4) (AA 744-761), (C-Term) antibodyHSD17B4 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4) (N-Term) antibodyHSD17B4 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4) antibodyKD Validated HSD17B4 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 25GB5635 unconjugated
anti-Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4) (AA 341-370) antibodyHSD17B4 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB31274 unconjugated
anti-Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4) (AA 340-370), (Middle Region) antibodyHSD17B4 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB 1:500-1:2000, IHC 1:50-1:200
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.3 mg/mL
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缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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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
- Store at -20°C. Avoid freeze / thaw cycles.
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- HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))
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别名
- HSD17B4
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背景
- The protein encoded by this gene 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.
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分子量
- 80 kDa
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UniProt
- P51659
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途径
- Monocarboxylic Acid Catabolic Process
抗原
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