Aromatase Antibodies, PA1-21398

Aromatase, a product of the CYP19A1 gene, is a member of the cytochrome P450 superfamily of monooxygenases that catalyze numerous reactions involved in drug metabolism and the synthesis of steroids, cholesterol, and other lipids. Aromatase is localized on the endoplasmic reticulum and catalyzes the formation of aromatic C18 estrogens from C19 androgens.

Aromatase is found in many tissues including the adrenal glands, gonads, placenta, skin, and adipose, as well as a number of abnormal tissues including those associated with endometriosis, uterine fibroids, breast cancer, and endometrial cancer. A surplus of aromatase leads to aromatase excess syndrome (AES), in which excess levels of estrogen result in heterosexual precocity in males and isosexual precocity in females. Furthermore, a lack of aromatase leads to aromatase deficiency (AROD), a rare disease in which fetal androgens are not converted into estrogens because of placental aromatase deficiency. This deficiency causes the virilization of female fetuses and primary amenorrhea, polycystic ovaries, breast hypoplasia, and tall stature in adult females.

Aromatase antibodies are commonly used in research applications such as western blot, immunohistochemistry, and immunofluorescence. Quality Invitrogen aromatase receptor antibodies are available for a variety of research needs.

See all aromatase antibodies

Featured product data

Immunohistochemical analysis of aromatase PA1-21398

Immunohistochemical analysis of aromatase using a specific polyclonal antibody (Cat. No. PA1-21398).

Western blot analysis using an aromatase polyclonal antibody PA5-14517

Western blot analysis using an aromatase polyclonal antibody (Cat. No. PA5-14517) in Jurkat cell lysates (35 µg per lane).

Immunofluorescent staining of HEPG2 cells using a specific aromatase antibody PA5-19633

Immunofluorescent staining of HEPG2 cells using a specific aromatase antibody (Cat. No. PA5-19633). The cells were fixed with formaldehyde (4%) for 10 minutes, permabilized with BSA (1%), normal goat serum (10%) and glycine (0.3 M) in 0.1% T-BST for 1 hour and exposed to the primary antibody at a concentration of 5 µg/mL overnight at 4°C. The secondary antibody was a FITC-conjugated goat anti-rabbit IgG (green) at a dilution of 1:1000. Plasma membranes were labeled with a WGA-594 fluorescent conjugate (red), and the nuclei stain was DAPI (blue).

Need antibodies in bulk quantities or custom packaging?
Inquire now. Complete Request Form

Want us to produce a custom antibody for you?
Learn more. Custom Antibody Services