本公司经销HMGCS2,三羟基三甲基辅酶A合成酶2抗体,克隆类型为polyclonal,宿主来源是Rabbit,HMGCS2三羟基三甲基辅酶A合成酶2抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!
本公司经销HMGCS2,三羟基三甲基辅酶A合成酶2抗体,克隆类型为polyclonal,宿主来源是Rabbit,HMGCS2三羟基三甲基辅酶A合成酶2抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!
货号:BY-5070R
英文名称:Anti-HMGCS2
中文名称:三羟基三甲基辅酶A合成酶2抗体
其他名称:名3 hydroxy 3 methylglutaryl Coenzyme A synthase 2 (mitochondrial); 3 hydroxy 3 methylglutaryl Coenzyme A synthase 2; 3 hydroxy 3 methylglutaryl coenzyme A synthase; HMG CoA synthase; HMGCS 2; Hydroxymethylglutaryl CoA synthase; Hydroxymethylglutaryl CoA synthase mitochondrial.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 57kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, mo, rat, hrs, cow, pig, dog, Rb
产品介绍:HMGCS2 is an enzyme that condenses acetyl CoA with acetoacetyl CoA to form HMG CoA, which is the substrate for HMG CoA reductase. Together with HMG CoA lyase, it is responsible for ketone body biosynthesis.Subcellular Location : Mitochondrion.Tissue Specificity : High expression in liver and colon. Low expression in testis, heart, skeletal muscle and kidney.Similarity : Belongs to the HMG-CoA synthase family.[DISEASE] Defects in HMGCS2 are the cause of HMG-CoA synthase deficiency (HMGCS deficiency) [MIM:605911]; also known as deficiency of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase 2. Affected individuals present with severe hypoketotic hypoglycemia, mild hepatomegaly, or fatty liver, and a nondiagnostic pattern of urinary organic acids with increase of medium and short chain dicarboxylic acids.