HeLa cells were subjected to SDS PAGE followed by western blot with FNab02462(DNAJC19 antibody) at dilution of 1:1000
Immunohistochemistry of paraffin-embedded human stomach using FNab02462(DNAJC19 antibody) at dilution of 1:100
Background
The protein encoded by this gene is thought to be part of a complex involved in the ATP-dependent transport of transit peptide-containing proteins from the inner cell membrane to the mitochondrial matrix. Defects in this gene are a cause of 3-methylglutaconic aciduria type 5 (MGA5), also known as dilated cardiomyopathy with ataxia (DCMA). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1, 2, 6, 10, 14 and 19.