GGEE1 Rabbit Polyclonal Antibody, 50ul Hepatocytes and distinctive facial features similar

and distinctive facial features similar to those found in Noonan syndrome

for 15mLx24

Mutations in this gene cause mitochondrial complex III deficiency

This gene is a member of the Ig superfamily and encodes a cell surface sialoglycoprotein expressed by cytokine-activated endothelium

Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIG

GGEE1 Rabbit Polyclonal Antibody, 50ul Hepatocytes and distinctive facial features similarThis gene is a member of family of proteins that are expressed in a variety of tumors and in some fetal and reproductive tissues. The encoded protein may protect cells from programmed cell death. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found.