Figure 1: Western Blot - Anti-alpha 2 Macroglobulin Antibody [ARC1734] (A308286)
Western blot analysis of extracts of HepG2 cells, using Anti-alpha 2 Macroglobulin Antibody [ARC1734] (A308286) at 1:1,000 dilution. The secondary antibody was Goat Anti-Rabbit IgG H&L Antibody (HRP) at 1:10,000 dilution. Lysates/proteins were present at 25µg per lane. The blocking buffer used was 3% non-fat dry milk in TBST. Detection was with a ECL Basic Kit. Exposure time: 90s.
Immunohistochemistry analysis of paraffin-embedded rat lung using Anti-alpha 2 Macroglobulin Antibody [ARC1734] (A308286) at a dilution of 1:100 (40x lens). Perform microwave antigen retrieval with 10 mM Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunohistochemistry analysis of paraffin-embedded human placenta using Anti-alpha 2 Macroglobulin Antibody [ARC1734] (A308286) at a dilution of 1:100 (40x lens). Perform microwave antigen retrieval with 10 mM Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunohistochemistry analysis of paraffin-embedded mouse kidney using Anti-alpha 2 Macroglobulin Antibody [ARC1734] (A308286) at a dilution of 1:100 (40x lens). Perform microwave antigen retrieval with 10 mM Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunofluorescence analysis of rat liver using Anti-alpha 2 Macroglobulin Antibody [ARC1734] (A308286)M)) Rabbit mAb (A9752) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of human liver using Anti-alpha 2 Macroglobulin Antibody [ARC1734] (A308286)M)) Rabbit mAb (A9752) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of mouse liver using Anti-alpha 2 Macroglobulin Antibody [ARC1734] (A308286)M)) Rabbit mAb (A9752) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
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