Products:Tags & Cell Markers >> Subcellular Markers >> Cytoskeleton >> Microtubules
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Could you please tell me what size band I'm supposed to get on a western blot using your ab7792 antibody,
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ANSWER: |
Around 55 kDa |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Anti-beta Tubulin antibody [TU-06] (ab7792) at 1/500 dilution + Human U87 MG whole cell lysate with 5% Milk for 1 hour at 22°C.
Secondary
HRP-conjugated Sheep anti-mouse IgG monoclonal at 1/5000 dilution
This image is courtesy of an anonymous Abreview
ICC/IF image of ab7792 stained HeLa cells. The cells were 4% PFA fixed (10 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 (ab7792, 1æg/ml) overnight at +4øC. The secondary antibody (green)ÿwas Alexa Fluor© 488 goat anti-mouse IgG (H+L) used at a 1/1000 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 1.43æM.
Overlay histogram showing HeLa cells stained with ab7792 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Triton X-100® 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 (ab7792, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
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