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)

this protein does not have immunosuppressant activity when complexed with FK506

The protein encoded by this gene is a serine proteinase that inhibits the activity of tissue-type plasminogen activator I

and is a receptor for C-C type chemokines

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