EHHADH 抗体 (Middle Region)
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北京 101111
Quick Overview for EHHADH 抗体 (Middle Region) (ABIN5514454)
抗原
See all EHHADH 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- Middle Region
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原理
- EHHADH Antibody - middle region
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序列
- VIAVDSDKNQ LATANKMITS VLEKEASKMQ QSGHPWSGPK PRLTSSVKEL
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产品特性
- This is a rabbit polyclonal antibody against ECHP. It was validated on Western Blot.
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纯化方法
- Affinity purified
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免疫原
- The immunogen is a synthetic peptide directed towards the middle region of Human ECHP
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应用备注
- Optimal working dilution should be determined by the investigator.
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说明
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP76113-100UG
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.5 mg/mL
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缓冲液
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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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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注意事项
- prevent freeze-thaw cycles
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储存条件
- 4 °C,-20 °C
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储存方法
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- EHHADH (Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH))
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别名
- EHHADH
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背景
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Background Information: The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.
Gene Name: enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase
Alternative Symbols: LBP, ECHD, LBFP, MFE1, PBFE, FRTS3, L-PBE
Protein Name: peroxisomal bifunctional enzyme
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分子量
- 79kDa
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基因ID
- 1962
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NCBI登录号
- NP_001957
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UniProt
- Q08426
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途径
- Monocarboxylic Acid Catabolic Process
抗原
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