S26A7 Rabbit Polyclonal Antibody, 50ul Metabolic enzymes tool compounds disease:Defects in NCF1 are the

disease:Defects in NCF1 are the cause of chronic granulomatous disease autosomal recessive cytochrome-b-positive type 1 (CGD1)

This protein is a cell growth-related protein

which are important in RNA binding and are known to be involved in RNA synthesis and metabolism

and downstream products

C17 is a cytokine-like protein specifically expressed in bone marrow and cord blood mononuclear cells that bear the CD34 (MIM 142230) surface marker

S26A7 Rabbit Polyclonal Antibody, 50ul Metabolic enzymes tool compounds disease:Defects in NCF1 are theThis gene is one member of a family of sulfate anion transporter genes. Family members are well conserved in gene structure and protein length yet have markedly different tissue expression patterns. This gene has abundant and specific expression in the kidney. Alternatively spliced transcript variants that encode different isoforms have been described.