产品名称:Propionyl-CoA carboxylase beta chain, mitochondrial ELISA Kit 检测范围:0.156-10 ng/mL 保存条件:2-8℃低温保存 保质期:6个月,所有试剂盒均提供批次。 试剂盒成分:酶标板,试剂,标准品等。 选型: 产品规格:96T/48T 96T指可以做94个标本-2个标准对照-84个样本 ...
产品名称:Propionyl-CoA carboxylase beta chain, mitochondrial ELISA Kit 检测范围:0.156-10 ng/mL 保存条件:2-8℃低温保存 保质期:6个月,所有试剂盒均提供批次。 试剂盒成分:酶标板,试剂,标准品等。 选型: 产品规格:96T/48T 96T指可以做94个标本-2个标准对照-84个样本 48T指可以做47个标本-1个标准对照-...
建议收到该Propionyl-CoA Carboxylase Beta Chain, Mitochondrial (PCCB) Antibody产品后,储存温度为-20°C。避免重复冻融其他 Abbexa总部位于英国剑桥的剑桥科学园,是一家专业的全球抗体供应商和蛋白质供应商,致力于为生命科学、药物开发和生物技术领域的科学家和研究者提供最佳的客户体验和高质量的产品。产品涵盖一抗...
针对PCCB (Propionyl-CoA carboxylase beta chain,mitochondrial) BioAssay ELISA Kit (Human)该产品的特点优势,欢迎查阅官网提供的产品说明书。保存建议 建议收到PCCB (Propionyl-CoA carboxylase beta chain,mitochondrial) BioAssay ELISA Kit (Human)产品后将其置于4°C至-20°C保存。其他...
Propionyl-CoA carboxylase beta chain, mitochondrial ELISA Kit 中文别名: FOR PROPIONYL-COA CARBOXYLASE BETA CHAIN, MITOCHONDRIAL ELISA KIT CBNumber: CB08118189 分子式: 分子量: 0 MOL File: Mol file 化学性质安全信息用途供应商1 Propionyl-CoA carboxylase beta chain, mitochondrial ELISA Kit化学性质 ...
(NAD/NADP), OGDHc: 2-oxoglutarate dehydrogenase complex, C-VOMIT: cholesterol, odd chain fatty acids, methionine, isoleucine, threonine, PCC: propionyl-CoA carboxylase, MUT: methylmalonyl-CoA mutase, MCEE: methylmalonyl-CoA epimerase, MMAA: Cobalamin A, MMAB: Cobalamin B, SS: succinate synthase...
Propionyl-CoA carboxylase propionyl Coenzyme A carboxylase, alpha polypeptide Identifiers Symbol PCCA Entrez 5095 HUGO 8653 OMIM 232000 RefSeq NM_000282
glycerol kinase; GPD1, glycerol-3-phosphate dehydrogenase 1; GPD2, glycerol -3-phosphate dehydrogenase 2; ACSS3, acyl CoA synthetase short chain family member 3; PCCA,propionyl CoA carboxylasealpha; PCCB,propionyl CoA carboxylasebeta; MCEE, methylmalonyl CoA epimerase; MUT, methylmalonyl CoA mutase...
A thioester derivative of propionic acid; an intermediate in the degradation of l-valine, l-isoleucine, l-threonine, l-methionine, and odd-chain fatty acids; a precursor for the synthesis of odd-chain fatty acids; it accumulates in individuals with a deficiency of propionyl-CoA carboxylase. ...
Propionyl CoA originates from the catabolism of essential amino acids (valine, threonine, isoleucine, methionine), odd-chain fatty acids, and cholesterol. It is primarily metabolized to methylmalonyl CoA by propionyl-CoA carboxylase (PCC), which, like other carboxylases, requires biotin for activity...