Anti-CYP3A7 antibody [F19 P2 H2]
| Name | Anti-CYP3A7 antibody [F19 P2 H2] |
|---|---|
| Supplier | Abcam |
| Catalog | ab55840 |
| Prices | $370.00 |
| Sizes | 100 µg |
| Host | Mouse |
| Clonality | Monoclonal |
| Isotype | IgG1 |
| Clone | F19 P2 H2 |
| Applications | WB IHC-P ELISA FC |
| Species Reactivities | Human |
| Antigen | Synthetic peptide derived from the C terminus of human CYP3A7 |
| Description | Mouse Monoclonal |
| Gene | CYP3A7 |
| Conjugate | Unconjugated |
| Supplier Page | Shop |
Product images
![All lanes : Anti-CYP3A7 antibody [F19 P2 H2] (ab55840) at 1 µg/mlLane 1 : molecular weight markersLane 2 : CYP3A4 recombinant proteinLane 3 : CYP3A7 recombinant proteinLane 4 : CYP3A5 recombinant proteinLane 5 : negative control](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_2/4458_ab55840wb.jpg)
All lanes : Anti-CYP3A7 antibody [F19 P2 H2] (ab55840) at 1 µg/mlLane 1 : molecular weight markersLane 2 : CYP3A4 recombinant proteinLane 3 : CYP3A7 recombinant proteinLane 4 : CYP3A5 recombinant proteinLane 5 : negative control
ab55840 at 1 µg/ml staining human prostate cancer tissue; formalin fixed, paraffin embedded.
![Overlay histogram showing HepG2 cells stained with ab55840 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab55840, 2µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_2/4460_CYP3A7-Primary-antibodies-ab55840-1.jpg)
Overlay histogram showing HepG2 cells stained with ab55840 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab55840, 2µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
Product References
Steroidogenic enzyme expression in the human fetal liver and potential role in - Steroidogenic enzyme expression in the human fetal liver and potential role in
O'Shaughnessy PJ, Monteiro A, Bhattacharya S, Fraser MJ, Fowler PA. Mol Hum Reprod. 2013 Mar;19(3):177-87.
Maternal smoking and fetal sex significantly affect metabolic enzyme expression - Maternal smoking and fetal sex significantly affect metabolic enzyme expression
O'Shaughnessy PJ, Monteiro A, Bhattacharya S, Fowler PA. J Clin Endocrinol Metab. 2011 Sep;96(9):2851-60.