GGEE1 Rabbit Polyclonal Antibody, 50ul Hepatocytes Mutations affecting this gene are

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

catalyzed by multisubunit complexes

The protein encoded by MATK has amino acid sequence similarity to Csk tyrosine kinase and has the structural features of the CSK subfamily: sRC homology SH2 and SH3 domains

Mutations in this gene cause mitochondrial complex III deficiency

Each one is individually vacuum-packed for ultimate sterility

GGEE1 Rabbit Polyclonal Antibody, 50ul Hepatocytes Mutations affecting this gene areThis 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.