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Figure 2 WB Validation in HeLa CellsLoading: 15 &956,g of lysate. Antibodies: NANOG 5585, 2 &956,g/mL , 1 h incubation at RT in 8% NFDM/TBST. Secondary: Goat Anti-Rabbit IgG HRP conjugate at 1:10,000 dilution. |
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Figure 3 Western Blot Validation in Mouse and Rat Testis Loading: 15 &956,g of lysates per lane. Antibodies: NANOG 5585, 2 &956,g/mL, 1h incubation at RT in 8% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10,000 dilution. |
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Figure 1 Immunoflouorescence Validation of NANOG in HeLa CellsImmunofluorescent analysis of PFA-fixed HeLa cells labeling NANOG with 5585 at 20 &956,g/mL, followed by goat anti-rabbit IgG secondary antibody at 1/1000 dilution (red) and DAPI staining (blue). Alpha tubulin was stained with anti-alpha tubulin antibody following by goat anti-mouse IgG secondary antibody (green). Images were captured with confocal microscopy. |
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Figure 4 Immunohistochemistry Validation of NANOG in Human Testis Immunohistochemical analysis of paraffin-embedded human testis tissue using anti-NANOG antibody (5585) at 5 &956,g/ml. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT, antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin. |
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Figure 5 Immunohistochemistry Validation of NANOG in Mouse Testis Immunohistochemical analysis of paraffin-embedded mouse testis tissue using anti-NANOG antibody (5585) at 2 &956,g/ml. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT, antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin. |
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Figure 6 Immunohistochemistry Validation of NANOG in Rat Testis Immunohistochemical analysis of paraffin-embedded rat testis tissue using anti-NANOG antibody (5585) at 2 &956,g/ml. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT, antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin. |