Various lysates were subjected to SDS PAGE followed by western blot with 67434-1-Ig (LIPG antibody) at dilution of 1:8000 incubated at room temperature for 1.5 hours. The membrane was stripped and reblotted with HRP-conjugated GAPDH Monoclonal antibody (HRP-60004) as loading control. This data was developed using the same antibody clone with 67434-1-PBS in a different storage buffer formulation.

human placenta tissue were subjected to SDS PAGE followed by western blot with 67434-1-Ig (LIPG antibody) at dilution of 1:3000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67434-1-PBS in a different storage buffer formulation.

HepG2 cells were subjected to SDS PAGE followed by western blot with 67434-1-Ig (LIPG antibody) at dilution of 1:8000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67434-1-PBS in a different storage buffer formulation.

HaCaT cells were subjected to SDS PAGE followed by western blot with 67434-1-Ig (LIPG antibody) at dilution of 1:8000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67434-1-PBS in a different storage buffer formulation.

HT-29 cells were subjected to SDS PAGE followed by western blot with 67434-1-Ig (LIPG antibody) at dilution of 1:8000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67434-1-PBS in a different storage buffer formulation.

Immunohistochemical analysis of paraffin-embedded human prostate cancer tissue slide using 67434-1-Ig (LIPG antibody) at dilution of 1:400 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 67434-1-PBS in a different storage buffer formulation.

Immunohistochemical analysis of paraffin-embedded human prostate cancer tissue slide using 67434-1-Ig (LIPG antibody) at dilution of 1:400 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 67434-1-PBS in a different storage buffer formulation.