DNJC2 Polyclonal Antibody, 20ul Culture Tubes Mutations in this gene cause

Mutations in this gene cause autosomal dominant nocturnal frontal lobe epilepsy type 4

most of which are necessary for proper CEP55 function

Hundreds of DRB1 alleles have been described and typing for these polymorphisms is routinely done for bone marrow and kidney t

The product of PPP2R2B (protein phosphatase 2 regulatory subunit Bbeta) belongs to the phosphatase 2 regulatory subunit B family

Meprins are multidomain zinc metalloproteases that are highly expressed in mammalian kidney and intestinal brush border membranes

DNJC2 Polyclonal Antibody, 20ul Culture Tubes Mutations in this gene causeThis gene is a member of the M phase phosphoprotein (MPP) family. The gene encodes a phosphoprotein with a J domain and a Myb DNA binding domain which localizes to both the nucleus and the cytosol. The protein is capable of forming a heterodimeric complex that associates with ribosomes, acting as a molecular chaperone for nascent polypeptide chains as they exit the ribosome. This protein was identified as a leukemia associated antigen and expression