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. 2004 Jul;15(7):3433–3449. doi: 10.1091/mbc.E03-05-0328

Table 2.

Quantification of cofilin, phospho-cofilin, and phalloidin fluorescence intensity in neurons overexpressing wt-LIMK1, LIMK1-kd, and Δ-LIM

Anti-cofilin (1 μg/ml) Golgi region Growth cones
Non transfected 1250 ± 65 1640 ± 20
wt-LIMK1 1225 ± 58 1750 ± 56
LIMK1-kd 1356 ± 46 1630 ± 48
Δ-LIM 1278 ± 84 1670 ± 38
Anti-phospho cofilin (0.5 μg/ml) Golgi region Growth cones
Nontransfected 458 ± 72 680 ± 26
wt-LIMK1 1852 ± 64a 2240 ± 44a
Δ-LIM 450 ± 24 2720 ± 28a
Anti-phospho cofilin (1 μg/ml) Golgi region Growth cones
Nontransfected 932 ± 68 1125 ± 55
LIMK1-kd 184 ± 15a 272 ± 14a
Rhodamine-phalloidin (0.2 μg/ml) Golgi region Growth cones
Nontransfected 249 ± 17 660 ± 24
wt-LIMK1 1246 ± 68a 1850 ± 48a
Δ-LIM 312 ± 32 2412 ± 18a
Rhodamine-phalloidin (0.5 μg/ml) Golgi region Growth cones
Nontransfected 383 ± 47 1256 ± 22
LIMK1-kd 52 ± 12a 325 ± 18a
S3A-Cofilin 65 ± 14a 420 ± 36a

Values represent the average fluorescent intensity expressed in pixels within a 5-μm area located in the central region of the Golgi apparatus or growth cones. 12-Bit images were used for this quantification. Scale, 0 (black) to 4095 (white). Each value is the mean ± SEM. At least 50 cells were measured for each experimental condition.

a

Values significantly different from those of nontransfected cells.