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Figure 4. Western blot analysis of low-speed, Triton X-100–soluble (S) and -insoluble (I) protein fractions from unsynchronized KE37 cells and of a highly enriched centrosome preparation (CTR). Proteins were probed with affinity-purified HsSpc98p IgG (left). A band at 103 kD is observed in all fractions, while highly enriched in the centrosome fraction. The same blot was subsequently probed with anti–γ-tubulin (right). Note the similar partition of both proteins in all fractions. 10 μg of Triton X-100–soluble and -insoluble proteins representing 2 × 105 and 6 × 105 cells, respectively, and ∼3 × 107 centrosomes were loaded.

Image published in: Tassin AM et al. (1998)

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