Raji cells were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

mouse lung tissue were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:300 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

HeLa cells were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

Raji cells were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

Raji cells were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

HeLa cells were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

HEK-293 cells were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

L02 cells were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

mouse testis tissue were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:300 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

Raji cells were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

Raji cells were subjected to SDS PAGE followed by western blot with 21264-1-AP (CTR9 antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

Immunohistochemical analysis of paraffin-embedded human breast cancer using 21264-1-AP (CTR9 antibody) at dilution of 1:200 (under 10x lens). This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

Immunohistochemical analysis of paraffin-embedded human breast cancer using 21264-1-AP (CTR9 antibody) at dilution of 1:200 (under 40x lens). This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

Immunohistochemical analysis of paraffin-embedded human colon cancer using 21264-1-AP (CTR9 antibody) at dilution of 1:100 (under 10x lens). This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

Immunohistochemical analysis of paraffin-embedded human colon cancer using 21264-1-AP (CTR9 antibody) at dilution of 1:100 (under 40x lens). This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.

Immunofluorescent analysis of Hela cells, using CTR9 antibody 21264-1-AP at 1:25 dilution and Rhodamine-labeled goat anti-rabbit IgG (red). This data was developed using the same antibody clone with 21264-1-PBS in a different storage buffer formulation.