MVK Polyclonal Antibody, 100ul Molecular Biology May be able to induce

May be able to induce the degradation of filamin-A

Defects in this gene cause congenital erythropoietic porphyria (Gunther's disease)

The expression of these transcripts is restricted to the salivary gland among the human tissues examined

Histone H3

ADPGK catalyzes the ADP-dependent phosphorylation of glucose to glucose-6-phosphate and may play a role in glycolysis

MVK Polyclonal Antibody, 100ul Molecular Biology May be able to induceMVK encodes the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, in isoprenoid and sterol synthesis. Mevalonate kinase deficiency caused by mutation of MVK results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises. Defects in this gene also cause hyperimmunoglobulinaemia D and periodic fever