Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of DMAP1 showing staining in the cytoplasm and nucleus of paraffin-treated human esophageal carcinoma tissue (right) compared with a negative control in the absence of primary antibody (left). Antigen retrieval was performed using 10mM sodium citrate (pH 6.0), microwaved for 8-15 min. Tissues were blocked in 3% H2O2-methanol for 15 min at room temperature, washed with ddH2O and PBS, and then incubated with ab2848 diluted by 3% BSA-PBS at a dilution of 1:100 overnight at 4°C in a humidified chamber. Tissues were washed extensively in PBST and detection was performed using an HRP-conjugated secondary antibody followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of DMAP1 showing staining in the cytoplasm and nucleus of paraffin-treated mouse brain tissue (right) compared with a negative control in the absence of primary antibody (left). Antigen retrieval was performed using 10mM sodium citrate (pH 6.0), microwaved for 8-15 min. Tissues were blocked in 3% H2O2-methanol for 15 min at room temperature, washed with ddH2O and PBS, and then incubated with ab2848 diluted by 3% BSA-PBS at a dilution of 1:100 overnight at 4°C in a humidified chamber. Tissues were washed extensively in PBST and detection was performed using an HRP-conjugated secondary antibody followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of DMAP1 showing staining in the cytoplasm and nucleus of paraffin-treated mouse uterus tissue (right) compared with a negative control in the absence of primary antibody (left). Antigen retrieval was performed using 10mM sodium citrate (pH 6.0), microwaved for 8-15 min. Tissues were blocked in 3% H2O2-methanol for 15 min at room temperature, washed with ddH2O and PBS, and then incubated with ab2848 diluted by 3% BSA-PBS at a dilution of 1:100 overnight at 4°C in a humidified chamber. Tissues were washed extensively in PBST and detection was performed using an HRP-conjugated secondary antibody followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.
All lanes : Anti-DMAP1 antibody - ChIP Grade (ab2848) at 1/1000 dilutionLane 1 : HL-60 cell lysateLane 2 : HeLa cell lysateLane 3 : Mouse brain cell lysateLysates/proteins at 25 µg per lane.
ab2848 staining DMAP1 in asynchronous HeLa cells in conjunction with a secondary goat anti-rabbit antibody conjugated to Cy3 ® (green). Cells were counterstained with DAPI (red) to show the nucleus. Please refer to abreview for further details.See Abreview
Anti-DMAP1 antibody - ChIP Grade (ab2848) at 1/500 dilution + whole cell lysate prepared from Xenopus laevis egg at 10 µgSecondaryHRP-Protein A at 1/1000 dilutiondeveloped using the ECL technique