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![Immunocytochemistry/Immunofluorescence: LAP1 Antibody (RL13) [NB120-2737] - Analysis of LAP1 using anti-LAP1 monoclonal antibody shows staining in NS-1 Cells.](http://images.novusbio.com/fullsize/LAP1-Antibody-RL13-Immunocytochemistry-Immunofluorescence-NB120-2737-img0009.jpg "Immunocytochemistry/Immunofluorescence: LAP1 Antibody (RL13) [NB120-2737] - Analysis of LAP1 using anti-LAP1 monoclonal antibody shows staining in NS-1 Cells.")
![Immunohistochemistry-Paraffin: LAP1 Antibody (RL13) [NB120-2737] - Immunohistochemistry was performed on rat lymph node tissue. To expose target protein, antigen was retreived. Endogenous peroxidases were blocked in 3% H202-methanol for 15 minutes and tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with a LAP1 mouse monoclonal antibody at a dilution of 1:50 overnight in a humidified chamber. Tissues were washed in PBST and detection was performed. DAB staining buffer was applied and tissues were counterstained with hematoxylin and prepped for mounting.](http://images.novusbio.com/fullsize/LAP1-Antibody-RL13-Immunohistochemistry-Paraffin-NB120-2737-img0008.jpg)
![Immunohistochemistry: LAP1 Antibody (RL13) [NB120-2737] - Immunohistochemistry was performed on rat breast tissue. To expose target protein, antigen was retreived. Endogenous peroxidases were blocked in 3% H202-methanol for 15 minutes and tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with a LAP1 mouse monoclonal antibody at a dilution of 1:50 overnight in a humidified chamber. Tissues were washed in PBST and detection was performed. DAB staining buffer was applied and tissues were counterstained with hematoxylin and prepped for mounting.](http://images.novusbio.com/fullsize/LAP1-Antibody-RL13-Immunohistochemistry-NB120-2737-img0006.jpg)
![Immunohistochemistry-Paraffin: LAP1 Antibody (RL13) [NB120-2737] - Immunohistochemistry was performed on rat colon tissue. To expose target protein, antigen was retreived. Endogenous peroxidases were blocked in 3% H202-methanol for 15 minutes and tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with a LAP1 mouse monoclonal antibody at a dilution of 1:20 overnight in a humidified chamber. Tissues were washed in PBST and detection was performed. DAB staining buffer was applied and tissues were counterstained with hematoxylin and prepped for mounting.](http://images.novusbio.com/fullsize/LAP1-Antibody-RL13-Immunohistochemistry-Paraffin-NB120-2737-img0007.jpg)