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Figure 4 Western Blot Validation in Rat Liver TissueLoading: 15 &956,g of lysates per lane.Antibodies: sRANK-L 3963 (A: 0.25 &956,g/mL and B: 0.5 &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 5 Immunohistochemistry Validation of sRANK-L in Human Liver Tissue Immunohistochemical analysis of paraffin-embedded human liver tissue using anti sRANK-L antibody (3963) 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 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 6 Immunohistochemistry and Induced Expression Validation of sRANK-L in Rat Osteogenic Compartment (Hassan et al., 2017) Protein analysis for sRANK-L by immunohistochemistry with anti-sRANK-L antibodies (3963) in rat osteogenic cells. Strong immunoreactivity is shown for sRANK-L in osteogenic cells at 18hr after upper jaw molar extraction as compared to baseline. |
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Figure 1 Western Blot Validation in Human Cell Lines Loading: 15 &956,g of lysates per lane.Antibodies: sRANK-L 3963 (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 1 Western Blot Validation in Mouse TissuesLoading: 15 &956,g of lysates per lane.Antibodies: sRANK-L 3963 (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 3 Western Blot Validation with Recombinant ProteinLoading: 30 ng of human sRANK-L recombinant protein per lane.Antibodies: sRANK-L 3963 (A: 1 &956,g/mL, B: 2 &956,g/mL and C: 4 &956,g/mL), 1h incubation at RT in 5% NFDM/TBST.Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.Observed at around 27kD. |