Anti-Human/Mouse ACAD8 Polyclonal Antibody

This gene encodes a member of the acyl-CoA dehydrogenase family of enzymes that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branch chained amino acids. The encoded protein is a mitochondrial enzyme that functions in catabolism of the branched-chain amino acid valine. Defects in this gene are the cause of isobutyryl-CoA dehydrogenase deficiency.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12879
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human ACAD8
Specificity Detected at comparable levels in all tissues examined (heart, lung, brain, skeletal muscle, pancreas and placenta). Weakly expressed in liver and kidney.
Isotype IgG
Reacitivity Human,Mouse
Clone
Uniprot Q9UKU7
Concentration 0.3 mg/mL
Dilution IHC 1:15-1:50
Formulation
Application IHC,ELISA
Other Names ACAD 8,ACAD-8,ACAD8,ACAD8,Activator-recruited cofactor 42 kDa component,Acyl CoA dehydrogenase family member 8,Acyl Coenzyme A dehydrogenase family member 8,Acyl-CoA dehydrogenase family member 8,ARC42,FLJ22590,IBD,Isobutyryl-CoA dehydrogenase,Isobutyryl-CoA dehydrogenase,mitochondrial,mitochondrial
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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