WB
Western blot analysis of GSTK1 using anti-GSTK1 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GSTK1 antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate.
IHC
IHC analysis of GSTK1 using anti-GSTK1 antibody.
GSTK1 was detected in a paraffin-embedded section of human breast cancer tissue. The tissue section was incubated with rabbit anti-GSTK1 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of GSTK1 using anti-GSTK1 antibody.
GSTK1 was detected in a paraffin-embedded section of mouse heart tissue. The tissue section was incubated with rabbit anti-GSTK1 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of GSTK1 using anti-GSTK1 antibody.
GSTK1 was detected in a paraffin-embedded section of rat heart tissue. The tissue section was incubated with rabbit anti-GSTK1 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IF-P
IF analysis of GSTK1 using anti-GSTK1 antibody.
GSTK1 was detected in a paraffin-embedded section of human breast cancer tissue. The tissue section was incubated with rabbit anti-GSTK1 Antibody at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red) was used as secondary antibody. The section was counterstained with DAPI (Blue).
IP
IP analysis of GSTK1 using anti-GSTK1 antibody in 293T whole cell lysate.
Western blot analysis of GSTK1 using anti- GSTK1 antibody.
Lane 1: 293T whole cell lysates(30ug),
Lane 2: Rabbit control IgG instead of anti- GSTK1 antibody in 293T whole cell lysate,
Lane 3: anti- GSTK1 antibody (2μg) + 293T whole cell lysate (500μg).
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti- GSTK1 antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate.
FC
Flow Cytometry analysis of HepG2 cells using anti-GSTK1 antibody.
Overlay histogram showing HepG2 cells stained with Anti-GSTK1 Antibody (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GSTK1 Antibody at 1:100 dilution for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.