WB
Western blot analysis of anti-CD36 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-CD36 antigen affinity purified monoclonal antibody and probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate.
IHC
Immunohistochemical staining of paraffin-embedded liver tissue within the normal limits using anti-CD36mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100°C for 10min, Dilution 1:50)
IHC
Immunohistochemical staining of paraffin-embedded Kidney tissue within the normal limits using anti-CD36mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 100°C for 10min, Dilution 1:50)
IHC
Immunohistochemical staining of paraffin-embedded Human tonsil within the normal limits using anti-CD36 mouse monoclonal antibody. (Heat-induced epitope retrieval by 1mM EDTA in 10mM Tris buffer (pH8.5) at 120°C for 3min) (1:500)
IHC
IHC analysis of CD36 using anti-CD36 antibody.
CD36 was detected in a paraffin-embedded section of mouse liver tissue. The tissue section was incubated with mouse anti-CD36 Antibody at a dilution of 1:200 and developed using HRP Conjugated mouse IgG Super Vision Assay Kit with DAB as the chromogen.
ICC/IF
Anti-CD36 mouse monoclonal antibody immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY CD36.
FC
HEK293T cells transfected with either overexpress plasmid (Red), compared to an IgG isotype control, (Green) or empty vector control plasmid (Blue) were immunostained by anti-CD36 antibody, and then analyzed by flow cytometry (1:100).