Goetzman ES, Alcorn JF, Bharathi SS, Uppala R, McHugh KJ, Kosmider B, Chen R, Zuo YY, Beck ME, McKinney RW, et al. Long- chain acyl-CoA dehydrogenase deficiency as a cause of pulmonary surfactant dysfunction. J Biol Chem 2014;289:10668-10679....
产品名称: Acyl-CoA Dehydrogenase, Very Long Chain Human Recombinant 产品型号: ENZ-250产品展商: 其它品牌产品文档: 无相关文档 简单介绍 Acyl-CoA Dehydrogenase, Very Long Chain Human RecombinantAcyl-CoA Dehydrogenase, Very Long Chain Human Recombinant 的详细介绍 Product...
Recombinant Human Acyl-CoA Dehydrogenase, Long Chain 供应商 ProSpec 产品货号 ENZ-190 产品报价 ￥询价/10ug ￥1mg ￥2ug 产品说明书 点击查看 购买方式 在线支付宝及网银支付、支票、现金、电汇,或拨打全国免费服务电话4006800868与我们联系. 产品新闻 ...
组织长链脂酰辅酶A脱氢酶(ACYL COA DEHYDROGENASE)活性比色法定量检测试剂盒 CAS号: 英文名: Colorimetric quantitative detection kit for tissue long-chain acyl-CoA dehydrogenase (ACYL COA DEHYDROGENASE) activity英文别名: Colorimetric quantitative detection kit for tissue long-chain acyl-CoA dehydrogenase (...
中文名:long-chain-acyl-CoA dehydrogenase,英文名:long-chain-acyl-CoA dehydrogenase,CAS:59536-74-2,MSDS.
Acyl-CoA DehydrogenasesAcyl-CoA Dehydrogenase, Long-ChainDiagnosis, DifferentialPrognosisMutationLong-chain acyl-CoA dehydrogenase deficiency; VLCAD Very-long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a defect of the mitochondrial betaoxidation of long-chain fatty acids. There are three......
产品名称ACADVL Acyl-CoA Dehydrogenase, Very Long Chain Human Recombinant Protein 产品描述ACADVL Human Recombinant produced in E.Coli is a non-glycosylated, polypeptide chain containing 636 amino acids (41-655 a.a.) and having a molecular mass of 68.5 kda. ACADVL contains 21 amino acid His-Tag...
产品名称 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 ...
Recombinant Human Acyl-CoA Dehydrogenase, Very Long Chain information, including chemical properties, structure, melting point, boiling point, density, formula, molecular weight, uses, prices, suppliers, SDS and more, available at Chemicalbook.
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...