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Figure 3 Western Blot Validation in 293 Cells Antibodies: ST2 3363, 1 &956,g/mL, 1h incubation at RT in 5% NFDM/TBST.Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.Lane A: In the absence of blocking peptideLane B: In the presence of blocking peptide |
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Figure 2 WB Validation in Human, Mouse, and Rat Cell Lines Loading: 15 &956,g of lysate per lane Antibodies: ST2 3363, 1 &956,g/mL , 1 h 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 ST2 in Human Lung Cancer TissueImmunofluorescent analysis of 4% paraformaldehyde-fixed human lung cancer tissue labeling ST2 with 3363 at 5 &956,g/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) DAPI staining (blue). |
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Figure 1 Immunoflouorescence Validation of ST2 in HeLa CellsImmunofluorescent analysis of PFA-fixed HeLa cells labeling ST2 with 3363 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 5 Immunofluorescence Validation of ST2 in Human Lung Immunofluorescent analysis of PFA-fixed human lung tissue labeling ST2 with 3363 at 10 &956,g/mL, followed by goat anti-rabbit IgG secondary antibody at 1/1000 dilution (red) and DAPI staining (blue |
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Figure 7 Immunofluorescence Validation of ST2 in Mouse Kidney Immunofluorescent analysis of PFA-fixed mouse kidney tissue labeling ST2 with 3363 at 10 &956,g/mL, followed by goat anti-rabbit IgG secondary antibody at 1/1000 dilution (red) and DAPI staining (blue) |
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Figure 8 Immunohistochemistry Validation of ST2 in Rat Kidney Immunohistochemical analysis of paraffin-embedded rat kidney tissue using anti-ST2 antibody (3363) 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 4 Western Blot Validation in Mouse Heart Loading: 15 &956,g of lysateAntibodies: ST2 3363, 1 &956,g/mL, 1h incubation at RT in 5% NFDM/TBST.Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution. |