Hydroxyacyl-CoA Dehydrogenase (HADH) Peptide
HADH
适用: 哺乳动物
宿主: 合成
BP, WB, IHC
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- 抗原 See all HADH products
- HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))
- 蛋白类型
- Synthetic
- 宿主
- 哺乳动物
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- 序列
- YPMGPFELLD YVGLDTTKFI VDGWHEMDAE NPLHQPSPSL NKLVAENKFG
- 产品特性
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A synthetic peptide for use as a blocking control in assays to test for specificity of HADH antibody,
Alternative Names: HADH control peptide, HADH antibody Blocking Peptide, Anti-HADH Blocking Peptide, Hydroxyacyl-Coenzyme A Dehydrogenase Blocking Peptide, HAD Blocking Peptide, HADH1 Blocking Peptide, HADHSC Blocking Peptide, HHF4 Blocking Peptide, M/SCHAD Blocking Peptide, MGC8392 Blocking Peptide, SCHAD Blocking Peptide
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- 应用备注
- Optimal conditions should be determined by the investigator
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- 缓冲液
- PBS
- 注意事项
- Avoid repeated freeze/thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- Store at -20 °C long term.
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- 抗原
- HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))
- 别名
- HAD Peptide, HADHSC Peptide, hadhsc Peptide, wu:fb66a11 Peptide, zgc:86777 Peptide, Hadhsc Peptide, HADH1 Peptide, HCDH Peptide, HHF4 Peptide, MSCHAD Peptide, SCHAD Peptide, AA409008 Peptide, AU019341 Peptide, AW742602 Peptide, Schad Peptide, hydroxyacyl-CoA dehydrogenase Peptide, hydroxyacyl-CoA dehydrogenase L homeolog Peptide, hydroxyacyl-Coenzyme A dehydrogenase Peptide, 3-hydroxyacyl-CoA dehydrogenase (short-chain) Peptide, Short chain 3-hydroxyacyl-CoA dehydrogenase Peptide, short chain 3-hydroxyacyl-coa dehydrogenase Peptide, putative short chain 3-hydroxyacyl-CoA dehydrogenase Peptide, HADH Peptide, hadh Peptide, hadh.L Peptide, Hadh Peptide, CNI02410 Peptide, Tc00.1047053509717.90 Peptide, Tc00.1047053510105.240 Peptide, LMJF_36_1140 Peptide
- 背景
- HADH functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene.
- 分子量
- 33 kDa
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