ICC/IF image of ab36625 stained HeLa cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody ab36625 at 1/200 dilution overnight at +4°C. The secondary antibody (green) was DyLight® 488 goat anti- mouse (ab96879) IgG (H+L) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
![All lanes : Anti-SRA1 antibody [7H1G1] (ab36625)Lane 1 : Molecular weight markerLane 2 : Truncated SRA recombinant proteinLane 3 : Ovary carcinoma tissue lysate](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_5/4789_ab36625_WB.gif)
All lanes : Anti-SRA1 antibody [7H1G1] (ab36625)Lane 1 : Molecular weight markerLane 2 : Truncated SRA recombinant proteinLane 3 : Ovary carcinoma tissue lysate
Immunohistochemical analysis of paraffin-embedded human bladder carcinoma tissue, showing nuclear and cytoplasmic localisation using anti-human SRA-1 antibody (ab36625) with DAB staining.
Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue, showing nuclear and cytoplasmic localisation using anti-human SRA-1 antibody (ab36625) with DAB staining.
![Overlay histogram showing MCF7 cells stained with ab36625 (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 (ab36625, 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 IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in MCF7 cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_5/4792_SRA1-Primary-antibodies-ab36625-1.jpg)
Overlay histogram showing MCF7 cells stained with ab36625 (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 (ab36625, 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 IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in MCF7 cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.