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Visualizing and Analyzing Branching Microtubule Nucleation Using Meiotic Xenopus Egg Extracts and TIRF Microscopy.

Author(s): King, Matthew; Petry, Sabine

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dc.contributor.authorKing, Matthew-
dc.contributor.authorPetry, Sabine-
dc.date.accessioned2023-12-14T18:17:59Z-
dc.date.available2023-12-14T18:17:59Z-
dc.date.issued2016en_US
dc.identifier.citationKing, Matthew, Petry, Sabine. (2016). Visualizing and Analyzing Branching Microtubule Nucleation Using Meiotic Xenopus Egg Extracts and TIRF Microscopy.. Methods Mol Biol, 1413 (77 - 85. doi:10.1007/978-1-4939-3542-0_6)en_US
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr1jw86n08-
dc.description.abstractMitotic and meiotic spindles consist primarily of microtubules, which originate from centrosomes and within the vicinity of chromatin. Indirect evidence suggested that microtubules also originate throughout the spindle, but the high microtubule density within the spindle precludes the direct observation of this phenomenon. By using meiotic Xenopus laevis egg extract and employing total internal reflection (TIRF) microscopy, microtubule nucleation from preexisting microtubules could be demonstrated and analyzed. Branching microtubule nucleation is an ideal mechanism to assemble and maintain a mitotic spindle, because microtubule numbers are amplified while preserving their polarity. Here, we describe the assays that made these findings possible and the experiments that helped identify the key molecular players involved.en_US
dc.format.extent77 - 85en_US
dc.languageengen_US
dc.language.isoen_USen_US
dc.relation.ispartofMethods in Molecular Biologyen_US
dc.rightsAuthor's manuscripten_US
dc.titleVisualizing and Analyzing Branching Microtubule Nucleation Using Meiotic Xenopus Egg Extracts and TIRF Microscopy.en_US
dc.typeJournal Articleen_US
dc.identifier.doidoi:10.1007/978-1-4939-3542-0_6-
dc.identifier.eissn1940-6029-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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