Western blot analysis of lysates from HepG2 cell line and mouse kidney, rat spleen tissue lysates(from left to right), using ACADL Antibody at 1:1000 at each lane.
Long-chain specific acyl-CoA dehydrogenase, mitochondrial, LCAD, ACADL
Product description
The protein encoded by this gene belongs to the acyl-CoA
dehydrogenase family, which is a family of mitochondrial
flavoenzymes involved in fatty acid and branched chain amino-acid
metabolism. This protein is one of the four enzymes that catalyze
the initial step of mitochondrial beta-oxidation of straight-chain
fatty acid. Defects in this gene are the cause of long-chain
acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic
hypoglycemia.1) Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010)
Immunogen
This ACADL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 14-43 amino acids from the N-terminal region of human ACADL.
Western blot analysis of lysates from HepG2 cell line and mouse kidney, rat spleen tissue lysates(from left to right), using ACADL Antibody at 1:1000 at each lane.
Application Notes
For WB starting dilution is: 1:1000:
Additional Information
Form
Liquid
Storage Instructions
Store at 4˚C for three months and -20˚C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.