Background：This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.
仕様
Synonyms：ACAT 1,ACAT,acat1,Acetoacetyl CoA thiolase,acetoacetyl Coenzyme A thiolase,Acetoacetyl-CoA thiolase,Acetyl CoA acetyltransferase,mitochondrial,Acetyl Coenzyme A acetyltransferase 1,Acetyl-CoA acetyltransferase,acetyl-coa acetyltransferase precursor,mitochondrial,Acetyl-CoA thiolase,mitochondrial,acetyl-Coenzyme A acetyltransferase 1,MAT,mitochondrial acetoacetyl-CoA thiolase,mitochondrial,RATACAL,T2,testicular tissue protein Li 198,THIL,THIL
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB,IHC
Concentration：1mg/ml
Immunogen：Recombinant protein of human ACAT1
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
Dilution：WB1：500 - 1：2000 IHC1：50 - 1：200
Gene_ID（human）：38
Swissprot：P24752
Isotype：IgG
Research Areas：Cancer, Metabolism, Signal transduction, Tags ＆ Cell Markers
