Anti-FOXG1 antibody [mAbcam 51774]
| Name | Anti-FOXG1 antibody [mAbcam 51774] |
|---|---|
| Supplier | Abcam |
| Catalog | ab51774 |
| Prices | $376.00 |
| Sizes | 100 µg |
| Host | Mouse |
| Clonality | Monoclonal |
| Isotype | IgG2a |
| Clone | mAbcam 51774 |
| Applications | WB FC |
| Species Reactivities | Human, Rat, Chicken, Bovine, Zebrafish |
| Antigen | Synthetic peptide conjugated to KLH derived from within residues 400 to the C-terminus of Human FOXG1 |
| Blocking Peptide | Human FOXG1 peptide |
| Description | Mouse Monoclonal |
| Gene | FOXG1 |
| Conjugate | Unconjugated |
| Supplier Page | Shop |
Product images
![Anti-FOXG1 antibody [mAbcam 51774] (ab51774) at 5 µg/ml + Brain (Human) Tissue Lysate - adult normal tissue (ab29466) at 10 µgSecondaryRabbit polyclonal to Mouse IgG - H&L (HRP) at 1/2000 dilutionPerformed under reducing conditions.](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_2/20399_ab51774_1_1.jpg)
Anti-FOXG1 antibody [mAbcam 51774] (ab51774) at 5 µg/ml + Brain (Human) Tissue Lysate - adult normal tissue (ab29466) at 10 µgSecondaryRabbit polyclonal to Mouse IgG - H&L (HRP) at 1/2000 dilutionPerformed under reducing conditions.
![Overlay histogram showing SHSY-5Y cells stained with ab51774 (red line). The cells were fixed with 4% paraformaldehyde (10 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 (ab51774, 1µg/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 IgG2a [ICIGG2A] (ab91361, 1µg/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_2/20400_FOXG1-Primary-antibodies-ab51774-1.jpg)
Overlay histogram showing SHSY-5Y cells stained with ab51774 (red line). The cells were fixed with 4% paraformaldehyde (10 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 (ab51774, 1µg/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 IgG2a [ICIGG2A] (ab91361, 1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.