FA2H 抗体 (AA 101-150)
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北京 101111
Quick Overview for FA2H 抗体 (AA 101-150) (ABIN8121400)
抗原
See all FA2H 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 101-150
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原理
- FA2H Antibody
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特异性
- FA2H Polyclonal Antibody detects endogenous levels of FA2H
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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 human FA2H. at AA range: 101-150
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亚型
- IgG
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anti-Fatty Acid 2-Hydroxylase (FA2H) (AA 121-148) antibody
FA2H 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal RB23881 unconjugated
anti-Fatty Acid 2-Hydroxylase (FA2H) (N-Term) antibodyFA2H 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Fatty Acid 2-Hydroxylase (FA2H) (AA 257-306) antibodyFA2H 适用: 人, 小鼠, 大鼠, Cow, 豚鼠, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Fatty Acid 2-Hydroxylase (FA2H) (C-Term) antibodyFA2H 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Fatty Acid 2-Hydroxylase (FA2H) antibodyFA2H 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Fatty Acid 2-Hydroxylase (FA2H) antibodyFA2H 适用: 人 WB 宿主: 小鼠 Monoclonal 1B5 unconjugated
anti-Fatty Acid 2-Hydroxylase (FA2H) antibodyFA2H 适用: 人 WB 宿主: 小鼠 Monoclonal 2E3 unconjugated
anti-Fatty Acid 2-Hydroxylase (FA2H) (AA 1-372) antibodyFA2H 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- WB 1:500-2000, ELISA 1:10000-20000
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限制
- 仅限研究用
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状态
- Liquid
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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
- Store at -20°C/1 year
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有效期
- 12 months
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- FA2H (Fatty Acid 2-Hydroxylase (FA2H))
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别名
- FA2H
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背景
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Synonyms: Fatty acid 2-hydroxylase (EC 1.-.-.-) (Fatty acid alpha-hydroxylase)
Background: This gene encodes a protein that catalyzes the synthesis of 2-hydroxysphingolipids, a subset of sphingolipids that contain 2-hydroxy fatty acids. Sphingolipids play roles in many cellular processes and their structural diversity arises from modification of the hydrophobic ceramide moiety, such as by 2-hydroxylation of the N-acyl chain, and the existence of many different head groups. Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia.[provided by RefSeq, Mar 2010],
Gene Name: FA2H
Protein Name: FA2H
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基因ID
- 79152
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UniProt
- Q7L5A8
抗原
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