VALIDATION IMAGES
Formalin-fixed and paraffin embedded rat brain labeled with Anti-AMPK alpha-1/PRKAA1 Polyclonal Antibody, Unconjugated (bs-1115R) at 1:200 followed by conjugation to the secondary antibody and DAB staining.
Formalin-fixed and paraffin embedded mouse colon labeled with Anti-AMPK alpha-1/PRKAA1 Polyclonal Antibody, Unconjugated (bs-1115R) at 1:200 followed by conjugation to the secondary antibody and DAB staining.
Formalin-fixed and paraffin embedded human kidney labeled with Anti-AMPK alpha-1 Polyclonal Antibody, Unconjugated (bs-1115R) at 1:200 followed by conjugation to the secondary antibody and DAB staining.
Human Hela lysates probed with AMPK alpha 1 Polyclonal Antibody, Unconjugated (bs-1115R) at 1:500 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:10000 for 60 min at 37˚C.
U937 cells were fixed with 4% PFA for 10min at room temperature,permeabilized with 0.1% PBST for 20 min at room temperature, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with AMPK alpha-1 Polyclonal Antibody(bs-1115R)at 1:100 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS, followed by secondary antibody incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).
Mouse spleen cells probed with AMPK alpha-1 Polyclonal Antibody, unconjugated (bs-1115R) at 1:100 dilution for 30 minutes compared to control cells (purple), secondary only (blue) and isotype control (orange)
HepG2 cells were fixed with 4% PFA for 10min at room temperature,permeabilized with 90% ice-cold methanol for 20 min at -20℃, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with AMPK alpha 1 Polyclonal Antibody(bs-1115R)at 1:100 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS, followed by secondary antibody incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).