HeLa cells were subjected to Tris-Acetate gel system followed by western blot with 18830-1-AP (1A6/DRIM antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 18830-1-PBS in a different storage buffer formulation.

HepG2 cells were subjected to SDS PAGE followed by western blot with 18830-1-AP (1A6/DRIM antibody at dilution of 1:300 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 18830-1-PBS in a different storage buffer formulation.

IP result of anti-1A6/DRIM (IP:18830-1-AP, 4ug; Detection:18830-1-AP 1:800) with HeLa cells lysate 4000ug. This data was developed using the same antibody clone with 18830-1-PBS in a different storage buffer formulation.

Immunofluorescent analysis of Hela cells, using UTP20 antibody 18830-1-AP at 1:50 dilution and Rhodamine-labeled goat anti-rabbit IgG (red). This data was developed using the same antibody clone with 18830-1-PBS in a different storage buffer formulation.

Immunofluorescent analysis of Hela cells, using UTP20 antibody 18830-1-AP at 1:25 dilution and Rhodamine-labeled goat anti-rabbit IgG (red). Blue pseudocolor = DAPI (fluorescent DNA dye). This data was developed using the same antibody clone with 18830-1-PBS in a different storage buffer formulation.

Immunofluorescent analysis of (10% Formaldehyde) fixed HeLa cells using 18830-1-AP (1A6/DRIM antibody) at dilution of 1:50 and Alexa Fluor 488-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L). This data was developed using the same antibody clone with 18830-1-PBS in a different storage buffer formulation.