WB
Western blot analysis of KCNQ2 using anti-KCNQ2 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Sh-sy5y whole cell lysates,
Lane 2: HEK293 whole cell lysates,
Lane 3: rat brain tissue lysates,
Lane 4: rat brain tissue lysates,
Lane 5: C6 whole cell lysates,
Lane 6: mouse brain tissue lysates,
Lane 7: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-KCNQ2 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 KCNQ2 using anti-KCNQ2 antibody.
KCNQ2 was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-KCNQ2 Antibody at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
IHC
IHC analysis of KCNQ2 using anti-KCNQ2 antibody.
KCNQ2 was detected in a paraffin-embedded section of human brain tissue. The tissue section was incubated with rabbit anti-KCNQ2 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
FC
Flow Cytometry analysis of C6 cells using anti-KCNQ2 antibody.
Overlay histogram showing C6 cells stained with anti-KCNQ2 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-KCNQ2 Antibody at 1:100 dilution for 30 min at 20°C. DyLight®488 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.