别称:HSD17B10 ELISA Kit,17-beta-hydroxysteroid dehydrogenase 10 ELISA Kit,17-beta-HSD 10 ELISA Kit,3-hydroxy-2-methylbutyryl-CoA dehydrogenase ELISA Kit,3-hydroxyacyl-CoA dehydrogenase type ELISA Kit 适应种属:人源 规格:48t/96t 存储:在2-8℃存储6个月 uniprot id:Q99714 应用:人3-羟酰基辅酶...
产品名称:Human 3-hydroxyacyl-CoA dehydrogenase type-2 (HSD17B10) ELISA Kit 产品型号:EKC32400 产品展商:Biomatik 产品文档:无相关文档 简单介绍 Human 3-hydroxyacyl-CoA dehydrogenase type-2 (HSD17B10) ELISA Kit Human 3-hydroxyacyl-CoA dehydrogenase type-2 (HSD17B10) ELISA Kit的详细介绍 ...
ERAB/HCD2抗体 英文名字 ERAB/HCD2 Antibody (3-hydroxyacyl-CoA dehydrogenase type-2) 供应商 Biovision 产品货号 3255-100 产品报价 ￥已停产 产品说明书 点击查看 购买方式 银行转账、电汇、支票、现金,在线支付宝及网银支付,或直接与我们电话联系400-6800-868....
The neurotoxin 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine (MPTP) impairs mitochondrial respiration and damages dopaminergic neurons as seen in Parkinson's disease (PD). Here, we report that L‐3‐hydroxyacyl‐CoA dehydrogenase type II/amyloid binding alcohol dehydrogenase (HADH II/ABAD), ...
3-hydroxyacyl-coa dehydrogenase 羟酰基辅酶A脱氢酶 双语对照 词典结果：3-hydroxyacyl-CoA dehydrogenase [医]3-羟酰基-辅酶A脱氢酶;以上结果来自金山词霸
最佳答案 回答者:网友 3-hydroxyacyl-coa dehydrogenase 羟酰基辅酶A脱氢酶 双语对照 词典结果: 3-hydroxyacyl-CoA dehydrogenase [医]3-羟酰基-辅酶A脱氢酶; 以上结果来自金山词霸推荐: 丙二酸二乙酯 Cas No: 105-53-3 对溴苯酚 Cas No: 106-41-2 对氨基苯酚 Cas No: 123-30-8 肉桂酸 Cas No: ...
Summary Peroxisomal β-oxidation proceeds from enoyl-CoA through d-3-hydroxyacyl-CoA to 3-ketoacyl-CoA by the d-3-hydroxyacyl-CoA dehydratase/d-3-hydroxy-acyl-CoA dehydrogenase bifunctional protein (d-bifunctional protein), and the oxidation of bile-acid precursors also has been suggested as bein...
3-羟酰辅酶A脱氢酶(3-Hydroxyacyl-CoA dehydrogenase)是一种参与脂肪酸代谢的酶。长链3-羟酰辅酶A脱氢酶缺乏是一种遗传性代谢疾病,也被称为长链脂肪酸氧化缺陷(long-chain fatty acid oxidation disorder)。该疾病是由于基因突变导致3-羟酰辅酶A脱氢酶的功能缺陷,进而影响脂肪酸的正常代谢。 长链3-羟酰辅酶A脱氢...
别 名 HAD; HADH; HADH1; HADHSC; HCDH; HCDH_HUMAN; HHF4; Hydroxyacyl CoA dehydrogenase; Hydroxyacyl-coenzyme A dehydrogenase; hydroxyacyl-coenzyme A dehydrogenase, mitochondrial; L 3 hydroxyacyl Coenzyme A dehydrogenase short chain; M SCHAD; Medium and short chain L 3 hydroxyacyl coenzyme A deh...
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,与基因突变密切相关。 3-羟酰辅酶A脱氢酶是参与脂肪酸代谢的酶,它在线粒体内催化3-羟酰辅酶A转化为3-酮酰辅酶A的反应。3-羟酰辅酶A脱氢酶缺乏症是由于基因突变...