1 / 4

Quantification of Western Blot Data in Figure |

Data normalized with β-tubulin, presented as ratio. Bars show means ± SEM. Statistical significance indicated. |

nomlanga-harper
Download Presentation

Quantification of Western Blot Data in Figure |

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Supplementary data c c c c cd d b a a a a b b ab a d d c b c a a d d d d a a b c Figure S1. Quantification of the Western blot data in figure 4C. The area density of each band was measured with a UVP gel document system. The data were normalized with β-tubulin and presented as ratio relative to the area density of β-tubulin. Bars represent means ± SEM. Bars with the same letters are not significantly different from each other (p>0.05).

  2. Supplementary data b b c b b a a b a a a a e a a a d c b b c d a a c bc ab ab a a Figure S2. Quantification of the Western blot data in figure 5C. The area density of each band was measured with a UVP gel document system. The data were normalized with β-tubulin and presented as ratio relative to the area density of β-tubulin. Bars represent means ± SEM. Bars with the same letters are not significantly different from each other (p>0.05).

  3. Supplementary data c c cd c d c b b a a a a d d a c b bc c b d d a a a a d d b b c c b c a a Figure S3. Quantification of the Western blot data in figure 6A. The area density of each band was measured with a UVP gel document system. The data were normalized with β-tubulin and presented as ratio relative to the area density of β-tubulin. Bars represent means ± SEM. Bars with the same letters are not significantly different from each other (p>0.05).

  4. Supplementary data d f d e d c c b b a ab a a d d a c b b b b b a a a c b d b c d a a a d d Figure S4. Quantification of the Western blot data in figure 6B. The area density of each band was measured with a UVP gel document system. The data were normalized with β-tubulin and presented as ratio relative to the area density of β-tubulin. Bars represent means ± SEM. Bars with the same letters are not significantly different from each other (p>0.05).

More Related