英文名称:Fish 3-hydroxyacyl CoA dehydrogenase (Hoad) ELISA Kit 用途:科研实验 产地:上海 品牌:科博瑞 包装规格:96T/48T 标记物:HRP标记物 样本:血清,血浆,唾液,尿液,组织,细胞上清,裂解液等 检测方法:酶联免疫法 应用:详见说明书 检测限:详见说明书 ...
3-羟酰辅酶A脱氢酶缺乏症的英文名字是3-Hydroxyacyl-CoA Dehydrogenase Deficiency。基因解码表明:3-羟酰辅酶A脱氢酶缺乏症是一种遗传性代谢疾病,主要由HADH基因的突变引起。HADH基因位于人类染色体4q25-q26区域。 已经发现多种HADH基因的突变与3-羟酰辅酶A脱氢酶缺乏症相关。这些突变导致3-羟酰辅酶A脱氢酶的功能...
酰基CoA脱氢酶4) HCDH 3-羟酰基辅酶A脱氢酶 1. Objective:To clone and express the HCDH gene 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。5) HOAD 3-羟酰辅酶A脱氢酶 1. These enzymes measured were glyceraldehydes-pho...
SCHADD代表“中/短链 3-羟酰基 CoA 脱氢酶缺乏症”,这种疾病其他名称:短链 3-羟酰辅酶 A 脱氢酶缺乏导致的高胰岛素性低血糖;SCHAD 缺乏导致的高胰岛素血症;由于谷氨酰胺脱氢酶缺乏而导致的高胰岛素血症 研究人员Clayton 等人首次报道了由 HADH 基因隐性突变引起的高胰岛素血症。2001年。先证者是一对非近亲结婚...
长链3-羟酰基辅酶A 脱氢酶缺乏症的英文名字是Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency。基因解码表明:是的,长链3-羟酰基辅酶A脱氢酶缺乏症是由基因突变引起的。这种疾病是由ACADVL基因的突变引起的,该基因编码长链3-羟酰基辅酶A脱氢酶(ACADVL)酶。这种酶在脂肪酸代谢中起着重要的作用,突变会导致酶...
hadh;hadhsc;hoad;wu:fb66a11;zgc:86777;hydroxyacyl-CoA dehydrogenase;hydroxyacyl-coenzyme A dehydrogenase, mitochondrial;L-3-hydroxyacyl-Coenzyme A dehydrogenase, short chain;hydroxyacyl-Coenzyme A dehydrogenase;3-羟酰辅酶A脱氢酶(HOAD);β-羟酰辅酶A脱氢酶(HOAD) ...
2) long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) 长链三羟基酰基辅酶A脱氢酶3) bayerite 三羟铝石 1. Effects of organic acids on sorption of cadmiumion on goethite and bayerite; 有机酸对针铁矿和三羟铝石吸附镉离子的影响 2. Adsorption processes of Cu2+ on synthetic goethite,hematite,δ-...
1.These enzymes measured were glyceraldehydes-phosphate dehydrogenase (GAPDH), glycerol-3-phosphate dehydrogenase (GDH), lactate dehydrogenase (LDH), and 3-hydroxyacyl-CoA dehydrogenase (HOAD).对3日龄粘虫雌蛾吊飞过程中4种相关酶3-羟酰辅酶A脱氢酶(HOAD)、3-磷酸甘油醛脱氢酶(GAPDH)、3-磷酸甘油脱氢...
In enzymology, a 3-hydroxyacyl-CoA dehydrogenase (EC 1.1.1.35) is an enzyme that catalyzes the chemical reaction. (S)-3-hydroxyacyl-CoA + NAD+ rightleftharpoons 3-oxoacyl-CoA + NADH + H+. Thus, the two substrates of this enzyme are (S)-3-hydroxyacyl-CoA and NAD+, whereas its 3 ...
中国第一批罕见病目录释义63 长链3-羟酰基辅酶A脱氢酶缺乏症 long chain 3-hydroxyacyl-CoA dehydrogenase deficiency