Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM) Peptide
ACADM
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM) products
- Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM)
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-ACADM antibody (Catalog #: ARP32788_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- 纯化方法
- Purified
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- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM)
- 别名
- ACAD1 Peptide, MCAD Peptide, MCADH Peptide, AU018656 Peptide, fb53e01 Peptide, wu:fb53e01 Peptide, zgc:111905 Peptide, zgc:56101 Peptide, zgc:76911 Peptide, acyl-CoA dehydrogenase medium chain Peptide, acyl-CoA dehydrogenase, C-4 to C-12 straight chain L homeolog Peptide, acyl-Coenzyme A dehydrogenase, medium chain Peptide, acyl-CoA dehydrogenase, C-4 to C-12 straight chain Peptide, ACADM Peptide, acadm.L Peptide, Acadm Peptide, acadm Peptide
- 背景
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ACADM Is the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Clinical phenotypes are associated with ACADM hereditary deficiency.This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Alias Symbols: ACAD1, MCAD, MCADH
Protein Interaction Partner: ACADM,SUMO4,USP20,USP50
Protein Size: 421 - 分子量
- 46 kDa
- 基因ID
- 34
- NCBI登录号
- NM_000016, NP_000007
- UniProt
- P11310
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