Various lysates were subjected to SDS PAGE followed by western blot with 68165-1-Ig (USP36 antibody) at dilution of 1:5000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 68165-1-PBS in a different storage buffer formulation.

Various lysates were subjected to SDS PAGE followed by western blot with 68165-1-Ig (USP36 antibody) at dilution of 1:5000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 68165-1-PBS in a different storage buffer formulation.

WB result of USP36 antibody (68165-1-Ig; 1:30000; incubated at room temperature for 1.5 hours) with sh-Control and sh-USP36 transfected HeLa cells. This data was developed using the same antibody clone with 68165-1-PBS in a different storage buffer formulation.

IP result of anti-USP36 (IP:68165-1-Ig, 4ug; Detection:68165-1-Ig 1:3000) with Jurkat cells lysate 2030 ug. This data was developed using the same antibody clone with 68165-1-PBS in a different storage buffer formulation.

Immunofluorescent analysis of (-20°C Ethanol) fixed HeLa cells using USP36 antibody (68165-1-Ig, Clone: 1A1B3 ) at dilution of 1:800 and Multi-rAb CoraLite ® Plus 488-Goat Anti-Mouse Recombinant Secondary Antibody (H+L) (RGAM002). This data was developed using the same antibody clone with 68165-1-PBS in a different storage buffer formulation.

1x10^6 U2OS cells were intracellularly stained with 0.25 ug USP36 Monoclonal antibody (68165-1-Ig, Clone:1A1B3) and CoraLite®488-Conjugated Goat Anti-Mouse IgG(H+L) (SA00013-1)(red), or 0.25 ug Mouse IgG1 isotype control Mouse McAb (66360-1-Ig, Clone: 1F8D3) (blue). Cells were fixed and permeabilized with Transcription Factor Staining Buffer Kit (PF00011). This data was developed using the same antibody clone with 68165-1-PBS in a different storage buffer formulation.