ALG1 Rabbit Polyclonal Antibody, 100ul Digital Burette Mutations in SLC4A11 have been

Mutations in SLC4A11 have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2

proliferation and apoptosis

All 3 proteins bind with high affinity to the ATPase domain of Hsc70 and inhibit its chaperone activity in a Hip-repressible manner

a developmental disorder caused by deletion of multiple genes at 7q11

ALG1 Rabbit Polyclonal Antibody, 100ul Digital Burette Mutations in SLC4A11 have beenThe enzyme encoded by this gene catalyzes the first mannosylation step in the biosynthesis of lipid linked oligosaccharides. This gene is mutated in congenital disorder of glycosylation type Ik.