Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human breast cancer tissue sections labelling NG2 with ab83508 at 1/50. 4μm-thick sections were deparaffinized in xylene, dehydrated through three alcohol changes. Endogenous peroxidase activity was quenched with 3% hydrogen peroxide in methanol. Antigen retrieval was performed in 96°C solution of 0.01 mol/L sodium citrate buffer (pH 6.0) for 30 minutes. Peroxidase/DAB, Rabbit/Mouse kit, after visualization, the sections were counterstained with hematoxylin. Hisg NG2 expression.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human breast cancer tissue sections labelling NG2 with ab83508 at 1/50. 4μm-thick sections were deparaffinized in xylene, dehydrated through three alcohol changes. Endogenous peroxidase activity was quenched with 3% hydrogen peroxide in methanol. Antigen retrieval was performed in 96°C solution of 0.01 mol/L sodium citrate buffer (pH 6.0) for 30 minutes. Peroxidase/DAB, Rabbit/Mouse kit, after visualization, the sections were counterstained with hematoxylin. Low NG2 expression.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human breast cancer tissue sections labelling NG2 with ab83508 at 1/50. 4μm-thick sections were deparaffinized in xylene, dehydrated through three alcohol changes. Endogenous peroxidase activity was quenched with 3% hydrogen peroxide in methanol. Antigen retrieval was performed in 96°C solution of 0.01 mol/L sodium citrate buffer (pH 6.0) for 30 minutes. Peroxidase/DAB, Rabbit/Mouse kit, after visualization, the sections were counterstained with hematoxylin. Negative NG2 expression.
5 x 106 SK-MEL-28 cells were incubated with 5µg of ab83508, followed by APC-GtxMs IgG incubation.
Immunofluorescence analysis of Human adult blood endothelial progenitor cells (left) and umbilical artery smooth muscle cells (right). NG2 was stained using ab83508 at 1/200 dilution. Nuclei were stained with DAPI (blue).