Table 1.
Sample | CEs (SpiCen300) | Asters (tubulin) |
---|---|---|
Centrosomes | 50 | 50 |
KICR | 50 | 0 |
KICR (extract) | 50 | 50 |
KICR (extract + 5 mM EDTA) | 50 | 50 |
KICR (extract + 100 mM EDTA) | 50 | 50 |
KICR (extract + 5 mM DMAP) | 50 | 50 |
KICR (extract + 50 mM DMAP) | 50 | 50 |
KICR (extract: G-25 Spin column) | 50 | 50 |
Coverslips containing centrosomes (CEs) or KICRs were treated with PEM buffer or treated high-speed extracts, washed, incubated with tubulin, fixed, and processed for immunofluorescence using antibodies to SpiCen300 and tubulin. Coverslips were then analyzed by counting 50 SpiCen300 staining CEs or KICRs and determining how many of these had corresponding asters, judged by the tubulin staining.