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Figure 2 Western Blot Validation in Human Skeletal Muscle Loading: 10 &956,g of lysates per lane.A&956,g ntibodies: LMX1A, 7087, 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 Skeletal Muscle Loading: 10 &956,g of lysates per lane.Antibodies: LMX1A, 7087, 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 Immunofluorescence Validation of LMX1A in HeLa CellsImmunofluorescent analysis of methanol-fixed HeLa cells labeling LMX1A with 7087 at 10 &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 Immunohistochemistry Validation of LMX1A in Human Brain Meningioma Immunohistochemical analysis of paraffin-embedded human brain meningioma using anti-LMX1A antibody (7087) 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 4730,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 Validation of LMX1A in Mouse Brain Tissue Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti- anti-LMX1A antibody (7087) 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 4730,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 7 Immunohistochemistry Validation of LMX1A in Rat Skeletal Muscle Tissue Immunohistochemical analysis of paraffin-embedded rat spleen tissue using anti-LMX1A antibody (7087) 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 Rat Skeletal Muscle Loading: 10 &956,g of lysates per lane.Antibodies: LMX1A, 7087, 1 &956,g/mL, 1h incubation at RT in 5% NFDM/TBST.Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution. |