ab53095 staining Glucose Transporter GLUT3 in human tonsil tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with formaldehyde and blocked with H2O2 for 10 minutes at 25°C; antigen retrieval was by heat mediation in EDTA pH 8.6 at 100°C for 20 minutes. Samples were incubated with primary antibody (1/200) for 20 minutes at 25°C. An undiluted HRP polymer-conjugated goat anti-rabbit IgG polyclonal was used as the secondary antibody.See Abreview
Human brain tissue labelled with ab53095 at a 1/50 dilution, either incubated with (right image) or without (left image) the peptide.
All lanes : Anti-Glucose Transporter GLUT3 antibody (ab53095) at 1/300 dilutionLane 1 : LOVO cell extractLane 2 : LOVO cell extract with peptide
ICC/IF image of ab53095 stained HepG2 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 (ab53095, 1µg/ml) overnight at +4°C. 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.