HMGCL belongs to the HMG-CoA
lyase family. It is a mitochondrial enzyme that catalyzes the final
step of leucine degradation and plays a key role in ketone body
formation. Mutations in this gene are associated with HMG-CoA lyase
deficiency. Alternatively spliced transcript variants encoding
different isoforms have been found for this gene. [provided by
RefSeq].1) Fu, Z., et al. J. Biol. Chem. 285(34):26341-26349(2010)
Immunogen
This HMGCL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 161-190 amino acids from the Central region of human HMGCL.
Western blot analysis in WiDr cell line lysates (35ug/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.