HXK I Polyclonal Antibody, 50ul Cell Proliferation Mutations in this gene have

Mutations in this gene have been associated with autosomal recessive limb-girdle muscular dystrophy and dilated cardiomyopathy

Binds progesterone

Multiple alternatively spliced transcript variants that encode different protein isoforms have been observed in this gene

levocabastine

subcellular location:Upon EGF stimulation

HXK I Polyclonal Antibody, 50ul Cell Proliferation Mutations in this gene haveHexokinases phosphorylate glucose to produce glucose 6 phosphate, the first step in most glucose metabolism pathways. HK1 encodes a ubiquitous form of hexokinase which localizes to the outer membrane of mitochondria. Mutations in HK1 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 specific.