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Journal Article

Purification of tubulin from porcine brain.

MPS-Authors
/persons/resource/persons219179

Gell,  Christopher
Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society;

/persons/resource/persons219170

Friel,  Claire
Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society;

/persons/resource/persons219025

Borgonovo,  Barbara
Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society;

/persons/resource/persons219118

Drechsel,  David N.
Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society;

/persons/resource/persons219253

Hyman,  Anthony A.
Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society;

/persons/resource/persons219249

Howard,  Jonathon
Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society;

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Citation

Gell, C., Friel, C., Borgonovo, B., Drechsel, D. N., Hyman, A. A., & Howard, J. (2011). Purification of tubulin from porcine brain. Methods in Molecular Biology (Clifton, N.J.), 777, 15-28.


Cite as: https://hdl.handle.net/21.11116/0000-0001-0A98-9
Abstract
Microtubules, polymers of the heterodimeric protein αβ-tubulin, give shape to cells and are the tracks for vesicle transport and chromosome segregation. In vitro assays to study microtubule functions and their regulation by microtubule-associated proteins require the availability of purified αβ-tubulin. In this chapter, we describe the process of purification of heterodimeric αβ-tubulin from porcine brain.