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Fig1: Western blot analysis of CD22 on human CD22 recombinant protein using anti-CD22 antibody at 1/1,000 dilution.
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Fig2: Western blot analysis of CD22 on HEK293 (1) and CD22-hIgGFc transfected HEK293 (2) cell lysate using anti-CD22 antibody at 1/1,000 dilution.
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ysis of CD22 on different cell lysate using anti-CD22 antibody at 1/1,000 dilution. Positive control: Line1: L1210 Line2: Hela Line3: HEK293 Line4: Jurkat Line5: OCM-1 Line6: A431 Line7: NIH/3T3
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Fig4: ICC staining CD22 (green) and Actin filaments (red) in Hela cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
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Fig5: Immunohistochemical analysis of paraffin-embedded human cervical cancer tissue using anti-CD22 antibody. Counter stained with hematoxylin.
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Fig6: Immunohistochemical analysis of paraffin-embedded human cerebellum tissue using anti-CD22 antibody. Counter stained with hematoxylin.
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Fig7: Flow cytometric analysis of Hela cells with CD22 antibody at 1/100 dilution (green) compared with an unlabelled control (cells without incubation with primary antibody; red).