WB
Western blot analysis of anti- Nesprin 2/SYNE2 antibody. The sample well of each lane was loaded with 30ug of sample under reducing conditions.
Lane 1: human 293T whole cell lysates,
Lane 2: human placenta tissue lysates,
Lane 3: monkey COS-7 whole cell lysates.
Use rabbit anti- Nesprin 2/SYNE2 1:1000, probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit.
IHC
IHC analysis of Nesprin 2/SYNE2 using anti-Nesprin 2/SYNE2 antibody.
Nesprin 2/SYNE2 was detected in a paraffin-embedded section of human penis squamous cell carcinoma tissue. The tissue section was incubated with rabbit anti-Nesprin 2/SYNE2 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
ICC/IF
IF analysis of Nesprin 2/SYNE2 using anti-Nesprin 2/SYNE2 antibody.
Nesprin 2/SYNE2 was detected in an immunocytochemical section of Hela cells. Dylight594-conjugated Anti-rabbit IgG Secondary Antibody (red)was used as secondary antibody. The section was counterstained with DAPI(Blue).
FC
Flow Cytometry analysis of U87 cells using anti-Nesprin 2/SYNE2 antibody.
Overlay histogram showing U87 cells stained with anti-Nesprin 2/SYNE2 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-Nesprin 2/SYNE2 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.