All lanes : Anti-FGFR3 (phospho Y724) antibody [EPR2281(3)] (ab155960) at 1/5000 dilution (unpurified)Lane 1 : MCF-7 cell lysate (untreated)Lane 2 : MCF-7 cell lysate (treated with pervanadate)Lysates/proteins at 10 µg per lane.SecondaryPeroxidase-conjugated goat anti-rabbit IgG (H+L) at 1/1000 dilution
All lanes : Anti-FGFR3 (phospho Y724) antibody [EPR2281(3)] (ab155960) at 20000 (purified)Lane 1 : MCF-7 cell lysate (untreated)Lane 2 : MCF-7 cell lysate (treated with pervanadate)Lysates/proteins at 10 µg per lane.SecondaryPeroxidase-conjugated goat anti-rabbit IgG (H+L) at 1/1000 dilution
Immunocytochemistry/Immunofluorescence analysis of MCF-7 cells treated with pervanadate labelling FGFR3 (phospho Y724) with purified ab155960 at 1/80 (red). Cells were fixed with 4% paraformaldehyde. An Alexa Fluor® 555-conjugated goat anti-rabbit IgG (1/200) was used as the secondary antibody. Counterstained with DAPI (blue).
Immunocytochemistry/Immunofluorescence analysis of untreated MCF-7 cells labelling FGFR3 (phospho Y724) with purified ab155960 at 1/80. Cells were fixed with 4% paraformaldehyde. An Alexa Fluor® 555-conjugated goat anti-rabbit IgG (1/200) was used as the secondary antibody. Counterstained with DAPI (blue).
Immunocytochemistry/Immunofluorescence analysis of MCF-7 cells treated with pervanadate labelling FGFR3 (phospho Y724) with unpurified ab155960 at 1/300 (red). Cells were fixed with 4% paraformaldehyde. An Alexa Fluor® 555-conjugated goat anti-rabbit IgG (1/200) was used as the secondary antibody. Counterstained with DAPI (blue).
Immunocytochemistry/Immunofluorescence analysis of untreated MCF-7 cells labelling FGFR3 (phospho Y724) with unpurified ab155960 at 1/300. Cells were fixed with 4% paraformaldehyde. An Alexa Fluor® 555-conjugated goat anti-rabbit IgG (1/200) was used as the secondary antibody. Counterstained with DAPI (blue).
ab155960 (unpurified) at 1/15 immunoprecipitating FGFR3 (phospho Y724) in MCF-7 cells treated with pervanadate. For western blotting, a peroxidase-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/1000).Blocking buffer and concentration: 5% NFDM/TBST.Diluting buffer and concentration: 5% NFDM /TBST.
ab155960 (purified) at 1/50 immunoprecipitating FGFR3 (phospho Y724) in MCF-7 cells treated with pervanadate. For western blotting, a peroxidase-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/1000).Blocking buffer and concentration: 5% NFDM/TBST.Diluting buffer and concentration: 5% NFDM /TBST.