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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Antibody detects endogenous levels of total PCCA.
This protein is a key enzyme in the catabolic pathway of odd-chain fatty acids, isoleucine, threonine, methionine, and valine. It is probably a dodecamer composed of six biotin-containing alpha subunits and six beta subunits. The protein is located in the mitochondrial matrix. Defects in PCCA are the cause o propionic acidemia type I (PA-1). PA-1 is a life-threatening disease characterized by episodic vomiting, lethargy and ketosis, neutropenia, periodic thrombocytopenia, hypogammaglobulinemia, develop-mental retardation, and intolerance to protein.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: PCCase subunit alpha; Propanoyl-CoA:carbon dioxide ligase subunit alpha; propionyl CoA-carboxylase alpha; Propionyl-CoA carboxylase alpha chain, mitochondrial; RP11-151A6.1
基因别名: C79630; PCCA
UniProt ID: (Mouse) Q91ZA3
Entrez Gene ID: (Mouse) 110821