Anti-Human/Mouse ACAD9 Polyclonal Antibody

This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12880
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human ACAD9
Specificity Ubiquitously expressed in most normal human tissues and cancer cell lines with high level of expression in heart, skeletal muscles, brain, kidney and liver.
Isotype IgG
Reacitivity Human,Mouse
Clone
Uniprot Q9H845
Concentration 0.2 mg/mL
Dilution IHC 1:15-1:50
Formulation
Application IHC,ELISA
Other Names Acyl CoA dehydrogenase 9,Acyl Coenzyme A dehydrogenase family,member 9,acyl-CoA dehydrogenase family member 9,mitochondrial,FLJ23533,MGC14452,NPD002,Very long chain acyl CoA dehydrogenase VLCAD
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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