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)

CD48 encodes a member of the CD2 subfamily of immunoglobulin-like receptors which includes SLAM (signaling lymphocyte activation molecules) proteins

and downstream products

We provide services for the production of engineered antibodies

airway brushings

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.