CYP18-2 Antibody is a polyclonal antibody raised against human CYP2C18, a liver enzyme critical for drug metabolism and steroid biosynthesis. It specifically binds to epitopes in the CYP2C18 protein, enabling its detection in research assays .
The antibody was developed using a recombinant fusion protein spanning amino acids of human CYP2C18. Key validation steps include:
Specificity: No cross-reactivity with closely related isoforms (e.g., CYP2C8, CYP2C9, CYP2C19) .
Sensitivity: Detects CYP2C18 at levels as low as 2.5 pmol/mg in human liver microsomes .
Functional Assays: While the antibody binds CYP2C18, it does not inhibit its enzymatic activity (e.g., diazepam N-demethylation) .
CYP2C18 is expressed at very low levels (<2.5 pmol/mg) in human liver microsomes compared to other CYP2C subfamily members (e.g., CYP2C8, CYP2C9) .
Its expression varies across cell lines, with detectable levels in certain hepatic models .
Though not directly related to human CYP2C18, studies on its Arabidopsis homolog AtCYP18-2 reveal roles in stress response. For example:
AtCYP18-2 regulates alternative splicing of heat shock genes (e.g., HSP101, HSFA2) under stress, ensuring thermotolerance .
Loss of AtCYP18-2 disrupts intron retention (IR) in stress-responsive transcripts, reducing functional protein production .
Western Blotting: Used to quantify CYP2C18 expression in hepatic tissues and cell lines .
Functional Studies: Helps investigate CYP2C18’s role in drug metabolism and disease associations.
| Antibody Target | Reactivity | Key Differentiation |
|---|---|---|
| CYP2C18 | Human, Mouse, Rat | Low cross-reactivity with CYP2C8/9/19 |
| CYP2C8 | Human | Targets omega-hydroxylation enzymes |
| CYP2C9 | Human | Focus on warfarin metabolism |