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We have ordered a couple of weeks ago 3 Abs for matrin3, TRBP2 and Mov10 proteins. We used those Abs for WB and none of them worked. TRBP2 (AB72110) it doesnt give any band after o/n or 2-3h RT even in 1/500 dilution and matrin3 (ab51081) Mov10 (ab80613) they really give many many bands but not the right ones. These Abs came together, is it possible that sth happen during transfer? Would you please help us with make them work? Alternatively, could you please consider change them with another lot that you know is working or another Ab for these mouse proteins? We are looking forward for your reply in your earliest convenience!! Thank you in advance!! |
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ANSWER: |
Thank you for contacting us. |
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I was wondering if I could get more information about this antibody (Mov10 Antibody ab80613). Has anyone used it successfully for a co-immunopreceipitation experiment? Thanks, |
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ANSWER: |
Thank you for your inquiry. Unfortunately, we do not know of a publication where this antibody was used in a co-IP experiment. I would like to reassure you that this antibody is tested and guaranteed for IP by our Abpromise. To co-IP a protein the protocol might have to be adjusted from normal IP. I can recommend to review our Protocol section and the recent webinar about IP from one of our IP experts. Please follow these links: http://www.abcam.com/index.html?pageconfig=resource&rid=11385 http://dev-pws1.abcam.com/blog/index.cfm/2011/11/17/Immunoprecipitation-Procedurespitfalls-and-protocol-tips I hope you will find this information helpful. Please do not hesitate to contact us with any further questions. |
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
All lanes : Anti-Mov10 antibody (ab80613) at 0.1 µg/ml
Lane 1 : HeLa whole cell lysate at 50 µg
Lane 2 : HeLa whole cell lysate at 15 µg
Lane 3 : HeLa whole cell lysate at 5 µg
Lane 4 : 293T whole cell lysate at 50 µg
Lane 5 : NIH3T3 whole cell lysate at 50 µg
developed using the ECL technique
Predicted band size : 114 kDa
Observed band size : 114 kDa
Exposure time : 3 minutes
Immunoprecipitation of HeLa whole cell lysate using ab80613 at 3µg/mg (lane 1) or control IgG (lane 2). Samples were analysed by Western blot using ab80613 at 1µg/ml.
Detection: Chemiluminescence with an exposure time of 30
seconds.
ICC/IF image of ab80613 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 (ab80613, 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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