CD59 Polyclonal Antibody, 20ul[BT-AP02383] Molecular Biologyn Defects in C1S are the

Defects in C1S are the cause of selective C1s deficiency

The encoded protein is known to play a role in cystic fibrosis and Huntington's disease

a membrane-bound receptor that modulates innate immune response

ACAD11 (acyl-CoA dehydrogenase family member 11) encodes an acyl-CoA dehydrogenase enzyme with a preference for carbon chain lengths between 20 and 26

ready to break down proteins for your most daring experiments

CD59 Polyclonal Antibody, 20ul[BT-AP02383] Molecular Biologyn Defects in C1S are theCYP20A1 (cytochrome P450 family 20 subfamily A member 1) encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases that catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein lacks one amino acid of the conserved heme binding site. It also lacks the conserved I helix motif AGX (D,E)T, suggesting that its substrate may carry its own