ISPD Rabbit Polyclonal Antibody, 20ul Fluorescent Staining cells from all PBD patients

cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle

Their protein structures resemble small leucine-rich proteoglycans found in the extracellular matrix

Available in a variety of colors to distinguish loops and needles of different specifications: white 1

Mutations in this gene have been associated with pontocerebellar hypoplasia type 2

ISPD Rabbit Polyclonal Antibody, 20ul Fluorescent Staining cells from all PBD patientsThis gene encodes a 2 C methyl D erythritol 4 phosphate cytidylyltransferase like protein. Mutations in this gene are the cause of Walker Warburg syndrome. Alternate splicing results in multiple transcript variants.