DESP Rabbit Polyclonal Antibody, 50ul Metabolic enzymes Defects in CD3E cause immunodeficiency

Defects in CD3E cause immunodeficiency

This gene likely encodes a member of the secernin family of proteins

The heterodimer formed with GATA proteins is essential to activate expression of genes such as NFE2

This gene encodes a member of the kelch-like family of proteins that share a common domain structure consisting of an N-terminal broad-complex| tramtrack| bric-a-brac/poxvirus and zinc finger domain and C-terminal kelch repeat motifs

also called triple-A syndrome or Allgrove syndrome

DESP Rabbit Polyclonal Antibody, 50ul Metabolic enzymes Defects in CD3E cause immunodeficiencyThis gene encodes a protein that anchors intermediate filaments to desmosomal plaques and forms an obligate component of functional desmosomes. Mutations in this gene are the cause of several cardiomyopathies and keratodermas including skin fragility woolly hair syndrome. Alternative splicing results in multiple transcript variants.