![ADH7 Antibody IHC of formalin-fixed and paraffin-embedded lung tissue followed by peroxidase-conjugated secondary antibody and DAB staining.](http://www.bioprodhub.com/system/product_images/ab_products/3/sub_1/2866_234434_1576152.jpg)
ADH7 Antibody IHC of formalin-fixed and paraffin-embedded lung tissue followed by peroxidase-conjugated secondary antibody and DAB staining.
![Confocal immunofluorescent of ADH7 Antibody with NCI-H460 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).](http://www.bioprodhub.com/system/product_images/ab_products/3/sub_1/2867_234436_1576156.jpg)
Confocal immunofluorescent of ADH7 Antibody with NCI-H460 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).
![Western blot of lysates from HepG2, SW480 cell line (from left to right), using ADH7 Antibody. Antibody was diluted at 1:1000 at each lane. A goat anti-rabbit IgG H&L (HRP) at 1:5000 dilution was used as the secondary antibody. Lysates at 35ug per lane.](http://www.bioprodhub.com/system/product_images/ab_products/3/sub_1/2868_234433_1615014.jpg)
Western blot of lysates from HepG2, SW480 cell line (from left to right), using ADH7 Antibody. Antibody was diluted at 1:1000 at each lane. A goat anti-rabbit IgG H&L (HRP) at 1:5000 dilution was used as the secondary antibody. Lysates at 35ug per lane.
![ADH7 Antibody flow cytometry of K562 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.](http://www.bioprodhub.com/system/product_images/ab_products/3/sub_1/2869_234435_1576154.jpg)
ADH7 Antibody flow cytometry of K562 cells (right histogram) compared to a negative control cell (left histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.