PKP3 Polyclonal Antibody, 100ul Transporters Defects in PEX7 cause peroxisome

Defects in PEX7 cause peroxisome biogenesis disorders (PBDs)

Protein transport

ATP binding cassette subfamily B member 10 is a member of the MDR/TAP subfamily

The upstream promoter is located in a differentially methylated region (DMR) and undergoes imprinting

The FYVE domain mediates the recruitment of proteins involved in membrane trafficking and cell signaling to phosphatidylinositol 3-phosphate-containing membranes

PKP3 Polyclonal Antibody, 100ul Transporters Defects in PEX7 cause peroxisomeThis gene encodes a member of the arm repeat (armadillo) and plakophilin gene families. Plakophilin proteins contain numerous armadillo repeats, localize to cell desmosomes and nuclei, and participate in linking cadherins to intermediate filaments in the cytoskeleton. This protein may act in cellular desmosome dependent adhesion and signaling pathways. Two transcript variants encoding different isoforms have been found for this gene.