WB
Western blot analysis of anti- PTRF/CAVIN1 antibody. The sample well of each lane was loaded with 30ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human A549 whole cell lysates,
Lane 3: rat heart tissue lysates,
Lane 4: rat lung tissue lysates,
Lane 5: mouse heart tissue lysates,
Lane 6: mouse lung tissue lysates.
Use rabbit anti- PTRF/CAVIN1 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 PTRF/CAVIN1 using anti-PTRF/CAVIN1 antibody.
PTRF/CAVIN1 was detected in a paraffin-embedded section of human thyroid cancer tissue. The tissue section was incubated with rabbit anti-PTRF/CAVIN1 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of PTRF/CAVIN1 using anti-PTRF/CAVIN1 antibody.
PTRF/CAVIN1 was detected in a paraffin-embedded section of mouse lung tissue. The tissue section was incubated with rabbit anti-PTRF/CAVIN1 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of PTRF/CAVIN1 using anti-PTRF/CAVIN1 antibody.
PTRF/CAVIN1 was detected in a paraffin-embedded section of rat lung tissue. The tissue section was incubated with rabbit anti-PTRF/CAVIN1 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 PTRF/CAVIN1 using anti-PTRF/CAVIN1 antibody.
PTRF/CAVIN1 was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-PTRF/CAVIN1 Antibody at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)was used as secondary antibody. The section was counterstained with DAPI (Blue).
FC
Flow Cytometry analysis of SiHa cells using anti-PTRF/CAVIN1 antibody.
Overlay histogram showing SiHa cells stained with anti-PTRF/CAVIN1 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-PTRF/CAVIN1 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.