Acyl-CoA dehydrogenases constitute a family of flavoproteins that catalyze the α,β-dehydrogenation of fatty acid acyl-CoA conjugates. While they differ widely in their specificity, they share the same basic chemical mechanism of α,β-dehydrogenation. Medium chain acyl-CoA dehydrogenase is probably...
组织脂酰辅酶a脱氢酶(acylcoadehydrogenase)总活性比色法定量检测试剂盒 产品规格 20次 有效成分含量 99 检测方法 比色法 样本 组织,细胞,线粒体,细菌等 保质期 6个月 标记物 尿液 储存条件 冷藏或-20℃ 用途范围 仅用于科学实验研究使用 是否进口 否 包装规格 盒装 售价 客服报价为准 产地 上海 运输 快递...
2) acyl-coA dehydorgenase 酰基辅酶A脱氢酶 3) HCDH 3-羟酰基辅酶A脱氢酶 1. Objective:To clone and express theHCDHgene fragment in E. 目的:克隆并在大肠杆菌中表达3-羟酰基辅酶A脱氢酶(3-hydroxyacyl-CoA dehydrogenase,HCDH)并制备其抗血清。
多种酰基辅酶A脱氢酶缺乏症(multiple acyl-CoA dehydrogenase deficiency,MADD)是一种常见的脂肪酸氧化代谢紊乱,属常染色体隐性遗传,于1976年由Przyrembel等首次报道。 MADD是由于编码线粒体的电子转运黄素蛋白(ETF)α或β亚单位或电子转运黄素蛋白一泛醌氧化还原酶[ETF - QO],又称电子转运黄素蛋白脱氢酶(ETFDH)...
acyl‐CoA dehydrogenaseacyl‐CoA oxidase α,β‐dehydrogenationmechanismsAcyl-CoA dehydrogenases constitute a family of flavoproteins that catalyze the α,β-dehydrogenation of fatty acid acyl-CoA conjugates. While they differ widely in their specificity, they share the same basic chemical mechanism of ...
短链酰基辅酶A脱氢酶缺乏症(Short-chain acyl-CoA dehydrogenase deficiency)分子诊断基因检测 短链酰基辅酶A脱氢酶缺乏症是一种罕见的遗传性代谢疾病,主要由于SCAD基因的突变导致短链脂肪酸代谢障碍。为了进行分子诊断基因检测,可以通过检测患者的DNA样本,特别是SCAD基因的序列,以确定是否存在突变。这种基因检测可以帮助医生...
网络释义 1. 脂肪酰辅酶A脱氢酶 acyl... ... acyl halide 酰基卤,酰基卤acyl-CoA dehydrogenase脂肪酰辅酶A脱氢酶acyl bromide 酰基溴,酰基溴 ... www.hujiang.com|基于9个网页 2. 酰基辅酶A脱氢酶 英汉常用生物学词汇_专业词汇... ... acute poisoning 急性中毒acyl-COA dehydrogenase〔脂〕酰基辅酶A脱氢...
by an unknown mechanism, to MCAD in the mitochondrial matrix, which chain-shortens these intermediates further to C4. The final cycle of oxidation requires SCAD, which is also a matrix enzyme. The roles of additional acyl-CoA dehydrogenases, including LCAD, ACAD9, and ACAD10, have...
英语解释 acyl-CoA dehydrogenase 汉语翻译 【化】 酰基辅酶A脱氢酶
极长链酰基辅酶A脱氢酶缺乏症(very long chain acyl-CoA dehydrogenase deficiency, VLCADD,MIM201475)是由于细胞线粒体内脂肪酸β氧化中的关键酶极长链酰基辅酶A脱氢酶(very long chain acyl-CoA dehydrogenase,VLCAD)基因先天缺陷所致的常染色体隐性遗传疾病,是一种较罕见的遗传代谢性疾病。极长链酰基辅酶A脱氢酶缺乏...