Anti-Human/Mouse/Rat ACADM Polyclonal Antibody

This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA06197
Size 100μl
Host Type Rabbit
Immunogen Synthesized peptide derived from the Internal region of human MCAD.
Specificity
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot P11310
Concentration 1mg/mL
Dilution WB 1:500-1:2000, ELISA 1:20000
Formulation
Application WB,ELISA
Other Names ACAD 1,ACAD1,Acadm,ACADM,Acyl coenzyme A dehydrogenase,Acyl coenzyme A dehydrogenase C 4 to C 12 straight chain,FLJ18227,FLJ93013,FLJ99884,MCAD,MCADH,Medium chain acyl CoA dehydrogenase,Medium chain fatty acyl CoA dehydrogenase,Medium chain specific acyl CoA dehydrogenase,Medium chain specific acyl CoA dehydrogenase mitochondrial,Medium-chain specific acyl-CoA dehydrogenase,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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