Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
Western blot analysis of AMPK Beta 2/PRKAB2 using anti-AMPK Beta 2/PRKAB2 antibody (PB0723). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Brain tissue lysates,
Lane 2: Rat Skeletal Muscle tissue lysates,
Lane 3: PANC whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AMPK Beta 2/PRKAB2 antigen affinity purified polyclonal antibody (PB0723) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for AMPK Beta 2/PRKAB2 at approximately 34 kDa. The expected band size for AMPK Beta 2/PRKAB2 is at 30 kDa.
IHC analysis of AMPK Beta 2/PRKAB2 using anti-AMPK Beta 2/PRKAB2 antibody (PB0723).
AMPK Beta 2/PRKAB2 was detected in a paraffin-embedded section of mouse intestine tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-AMPK Beta 2/PRKAB2 Antibody (PB0723) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of AMPK Beta 2/PRKAB2 using anti-AMPK Beta 2/PRKAB2 antibody (PB0723).
AMPK Beta 2/PRKAB2 was detected in a paraffin-embedded section of rat intestine tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-AMPK Beta 2/PRKAB2 Antibody (PB0723) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of AMPK Beta 2/PRKAB2 using anti-AMPK Beta 2/PRKAB2 antibody (PB0723).
AMPK Beta 2/PRKAB2 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-AMPK Beta 2/PRKAB2 Antibody (PB0723) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of A431 cells using anti-AMPK Beta 2/PRKAB2 antibody (PB0723).
Overlay histogram showing A431 cells stained with PB0723 (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-AMPK Beta 2/PRKAB2 Antibody (PB0723) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) 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.
IF analysis of AMPK Beta 2/PRKAB2 using anti-AMPK Beta 2/PRKAB2 antibody (PB0723).
AMPK Beta 2/PRKAB2 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-AMPK Beta 2/PRKAB2 Antibody (PB0723) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Western blot analysis of AMPK Beta 2/PRKAB2 using anti-AMPK Beta 2/PRKAB2 antibody (PB0723). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Brain tissue lysates,
Lane 2: Rat Skeletal Muscle tissue lysates,
Lane 3: PANC whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AMPK Beta 2/PRKAB2 antigen affinity purified polyclonal antibody (PB0723) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for AMPK Beta 2/PRKAB2 at approximately 34 kDa. The expected band size for AMPK Beta 2/PRKAB2 is at 30 kDa.
IHC analysis of AMPK Beta 2/PRKAB2 using anti-AMPK Beta 2/PRKAB2 antibody (PB0723).
AMPK Beta 2/PRKAB2 was detected in a paraffin-embedded section of mouse intestine tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-AMPK Beta 2/PRKAB2 Antibody (PB0723) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of AMPK Beta 2/PRKAB2 using anti-AMPK Beta 2/PRKAB2 antibody (PB0723).
AMPK Beta 2/PRKAB2 was detected in a paraffin-embedded section of rat intestine tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-AMPK Beta 2/PRKAB2 Antibody (PB0723) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of AMPK Beta 2/PRKAB2 using anti-AMPK Beta 2/PRKAB2 antibody (PB0723).
AMPK Beta 2/PRKAB2 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-AMPK Beta 2/PRKAB2 Antibody (PB0723) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of A431 cells using anti-AMPK Beta 2/PRKAB2 antibody (PB0723).
Overlay histogram showing A431 cells stained with PB0723 (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-AMPK Beta 2/PRKAB2 Antibody (PB0723) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) 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.
IF analysis of AMPK Beta 2/PRKAB2 using anti-AMPK Beta 2/PRKAB2 antibody (PB0723).
AMPK Beta 2/PRKAB2 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-AMPK Beta 2/PRKAB2 Antibody (PB0723) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).