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Figure 4 Western Blot Validation in Jurkat Cell LysateLoading: 15 &956,g of lysates per lane.Antibodies: IKK epsilon 2329 (2 &956,g/mL), 1h incubation at RT in 5% NFDM/TBST.Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution. |
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Figure 6 Immunofluorescence Validation of IKK epsilon in HeLa CellsImmunofluorescent analysis of 4% paraformaldehyde-fixed HeLa cells labeling IKK epsilon with 2329 at 20 &956,g/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue). |
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Figure 5 Immunohistochemistry Validation of IKK epsilon in Human Pancreas Tissue Immunohistochemical analysis of paraffin-embedded human pancreas tissue using anti-IKK epsilon antibody (2329) at 10 &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 4&730,C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin. |
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Figure 1 Induction Validation in Mouse Cell LineLoading: 15 &956,g of Raw264.7 cell lysates per lane.Antibodies: IKK epsilon 2329 (1 &956,g/mL), 1h incubation at RT in 5% NFDM/TBST.Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.Cells were treated with LPS (0.3 &956,g/mL) for 3 hrs (lane 2) and 6 hrs (lane 3) or with control (lane 1). |
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Figure 2 Western Blot Validation in Human and Mouse Cell LinesLoading: 15 &956,g of lysates per lane.Antibodies: IKK epsilon 2329 (1 &956,g/mL), 1h incubation at RT in 5% NFDM/TBST.Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution. |
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Figure 3 Western Blot Validation in Mouse Tissue LysatesLoading: 15 &956,g of lysates per lane.Antibodies: IKK epsilon 2329 (2 &956,g/mL), 1h incubation at RT in 5% NFDM/TBST.Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution. |