Application
Immunofluorescence staining of LAMP1 (red) in HeLa cells.
Application
Western blot analysis of LAMP1 was performed by loading 20 μg of HeLa cell lysate and 5 μl of Molecular Weight Protein Ladder per well onto a 4-12% Bis-Tris polyacrylamide gel. Proteins were transferred to a nitrocellulose membrane and blocked with 5% BSA/TBST for at least 1 hour. The membrane was probed with an anti-LAMP1 polyclonal antibody at a dilution of 1:500 for one hour at room temperature, washed in TBS-0.1%Tween-20, and probed with a goat anti-rabbit IgG-HRP secondary antibody.