SUH Polyclonal Antibody, 100ul Centrifugal Filter Defects in PEX7 cause peroxisome

Defects in PEX7 cause peroxisome biogenesis disorders (PBDs)

EPHA2 belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family

The protein encoded by this gene is a negative regulator of autophagy and endocytic trafficking and controls endosome maturation

This gene encodes a member of the lipoxygenase family of structurally related nonheme iron dioxygenases involved in the production of fatty acid hydroperoxides

EDG-2) is a 144 amino acid protein encoded by the human gene BUD31

SUH Polyclonal Antibody, 100ul Centrifugal Filter Defects in PEX7 cause peroxisomeThe protein encoded by this gene is a transcriptional regulator important in the Notch signaling pathway. The encoded protein acts as a repressor when not bound to Notch proteins and an activator when bound to Notch proteins. It is thought to function by recruiting chromatin remodeling complexes containing histone deacetylase or histone acetylase proteins to Notch signaling pathway genes. Several transcript variants encoding different isoforms have