WB
Western blot analysis of L-Plastin/LCP1 using anti-L-Plastin/LCP1 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HL-60 whole cell lysates,
Lane 2: human THP-1 whole cell lysates,
Lane 3: human Hela whole cell lysates,
Lane 4: rat spleen tissue lysates,
Lane 5: mouse spleen tissue lysates,
Lane 6: mouse RAW264.7 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-L-Plastin/LCP1 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 L-Plastin/LCP1 using anti-L-Plastin/LCP1 antibody.
L-Plastin/LCP1 was detected in a paraffin-embedded section of human B lymphocytic tumor tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-L-Plastin/LCP1 Antibody at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
FC
Flow Cytometry analysis of U2OS cells using anti-LCP1 antibody.Overlay histogram showing U2OS cells stained with anti-LCP1 antibody (Blue line).Fluoro®488 conjugated goat anti-rabbit IgG was used as secondary antibody Isotype control antibody (Green line) was rabbit IgG (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
ICC/IF
ICC/IF analysis of L-Plastin/LCP1 using anti-L-Plastin/LCP1 antibody.
L-Plastin/LCP1 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-L-Plastin/LCP1 Antibody at a dilution of 1:100. Fluoro488 Conjugated Goat Anti-Rabbit IgG (Green) was used as secondary antibody. The section was counterstained with DAPI (Blue).