HXK I Monoclonal Antibody, 100ul[BT-MCA0759] Cellular Function Assays The peroxisome biogenesis disorders (PBDs)

The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive

It plays an important role in the development of the brain and exerts its effects on specific neurons in the nervous system

with the highest level of expression in the testes

The encoded protein is activated by the guanine nucleotide exchange factor PREB and is involved in protein transport from the endoplasmic reticulum to the Golgi

but does not abolish

HXK I Monoclonal Antibody, 100ul[BT-MCA0759] Cellular Function Assays The peroxisome biogenesis disorders (PBDs)Hexokinases phosphorylate glucose to produce glucose 6 phosphate, the first step in most glucose metabolism pathways. This gene encodes a ubiquitous form of hexokinase which localizes to the outer membrane of mitochondria. Mutations in this gene have been associated with hemolytic anemia due to hexokinase deficiency. Alternative splicing of this gene results in several transcript variants which encode different isoforms, some of which are tissue