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| 货号 | 规格 | 可用库存 | 销售价(RMB) | 您的折扣价(RMB) | 购买数量 |
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| 熔点: | |
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| 储存条件: | -20℃ |
Anti-AURKA antibody [A4-8D]
WB: 1:500-1:2,000
ICC: 1:50-1:200
IHC-P: 1:50-1:200
FC: 1:50-1:100

Fig1: Western blot analysis of Aurora A on human Aurora A recombinant protein using anti- Aurora A antibody at 1/1,000 dilution.

Fig2: Western blot analysis of Aurora A on HEK293 (1) and Aurora A -hIgGFc transfected HEK293 (2) cell lysate using anti- Aurora A antibody at 1/1,000 dilution.

Fig3: Western blot analysis of Aurora A on different cell lysate using anti- Aurora A antibody at 1/1,000 dilution.
Positive control: Line1: HEK293 Line2: MCF-7 Line3: Hela

Fig4: ICC staining Aurora A (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.

Fig5: ICC staining Aurora A (green) and Actin filaments (red) in SMMC-7721 cells. The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

Fig6: Immunohistochemical analysis of paraffin-embedded human cervical cancer tissue using anti- Aurora A antibody. Counter stained with hematoxylin.

Fig7: Immunohistochemical analysis of paraffin-embedded human rectum cancer tissue using anti- Aurora A antibody. Counter stained with hematoxylin.

Fig8: Flow cytometric analysis of Hela cells with Aurora A antibody at 1/100 dilution (green) compared with an unlabelled control (cells without incubation with primary antibody; red).
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