PEX12 Polyclonal Antibody, 50ul Cryopreservation Contains 2 fibronectin type-III domains

Contains 2 fibronectin type-III domains

It is possible that alternative splicing of this gene may be physiologically important in the regulation of target genes

Mutations in this gene are associated with desmin-related myopathy

Prelamin A is farnesylated and carboxymethylated on the cysteine residue of a carboxyl-terminal CaaX motif

PEX12 Polyclonal Antibody, 50ul Cryopreservation Contains 2 fibronectin type-III domainsThis gene belongs to the peroxin 12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being