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. 2001 Dec 24;155(7):1159–1172. doi: 10.1083/jcb.200105093

Table II.

Integrated fluorescence of kinetochores from nocodazole cells treated ± ATP inhibitors and immunostained for various spindle checkpoint components and motor proteins

Kinetochores Saline Azide/DOG Washout
Mad2
n 27 28 29
mean ± SD 4.6 ± 1.0 4.1 ± 0.8 4.4 ± 0.8
ratio to control 1 0.89 0.96
BubR1
n 46 31 36
mean ± SD 9.2 ± 2.0 7.2 ± 2.9 9.0 ± 2.2
ratio to control 1 0.78 0.98
CENP-E
n 30 40 30
mean ± SD 21.6 ± 12.1 19.5 ± 7.4 23.1 ± 3.9
ratio to control 1 0.90 1.07
Dynein
n 40 26 24
mean ± SD 2.4 ± 1.1 2.5 ± 0.6 2.4 ± 0.5
ratio to control 1 1.04 1
3F3/2
n 46 30 44
mean ± SD 15.7 ± 5.1 7.4 ± 3.9 12.2 ± 3.1
ratio to control 1 0.47 0.78

Integrated kinetochore fluorescence was measured using identical imaging conditions. With the exception of BubR1 and 3F3/2, all other kinetochore components demonstrated similar mean fluorescence intensities after azide/DOG treatment when compared to saline and washout treatment (P > 0.01). n = number of kinetochores measured per condition. Mean ± SD = actual values/1,000.