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Thanks for getting back to me with this information. We actually want to use this antibody to detect endogenous BMP-1 in HepG2 cells by western blot, will we still be covered under the Abpromise guarantee for this? If so then I will look into ordering the product and we will test it on our cell lysates. |
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ANSWER: |
Thank you for getting back to me. |
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Phone call requesting information on if the antibody had been used to detect endogenously expressed protein for western blotting. |
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ANSWER: |
I am sorry for the delay in getting back to you in regards to anti-BMP1 antibody (ab38952). |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
ICC/IF image of ab38952 stained HepG2 cells. The cells were 4% formaldehyde 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 (ab38952, 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.
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