Products:Cell Biology >> Apoptosis >> Intracellular >> Bcl2 Family
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Dear Technical service, |
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ANSWER: |
Thank you for contacting us. |
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Ordered ab90435 by mistake and would like to return it. |
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ANSWER: |
Thank you for contacting Abcam. |
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Good afternoon, I ordered the rabbit monoclonal antibody BAD several months ago. I now have the question if you could let me know if the antibody binds to (immunohistochemistry) the unphosphorylated or phosphorylated form of BAD? Thank you for your help! |
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ANSWER: |
Thank you for contacting us.
I can confirm that this antibody does recongize the phosphorylated and unphosphorylated form of BAD. Indeed, there is no phosphorylation site on the immunogen sequences used for this antibody.
I hope this information is helpful to you. Please do not hesitate to contact us if you need any more advice or information. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Anti-Bad antibody [Y208] (ab32445) at 1/5000 dilution + Hela cell lysate
Predicted band size : 18 kDa
Observed band size : 23 kDa (why is the actual band size different from the predicted?)
Immunohistochemical staining of paraffin-embedded human lymphoma using ab32445 at 1/100 dilution.
ICC/IF image of ab32445 stained MCF7 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 (ab32445, 1µg/ml) overnight at +4ºC. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit 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 1.43µM.
Overlay histogram showing MCF-7 cells stained with ab32445 (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 (ab32445, 1/20 dilution) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (
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