Literature DB >> 27193839

Using Fluorescence Microscopy to Study Mitosis.

Sai K Balchand1, Barbara J Mann1, Patricia Wadsworth2.   

Abstract

Fluorescence microscopy is one of the most important approaches in the cell biologist's toolbox for studying the mitotic spindle. In fact, many of the key insights into our understanding of mitosis have been enabled by the visualization of mitotic processes using fluorescence microscopy. Here, we summarize some of the important considerations for imaging mitosis using fluorescence microscopy. Because light can damage live cells, we emphasize the importance of minimizing cellular damage while obtaining informative images.

Entities:  

Keywords:  Confocal laser scanning microscopy; Mitosis; Spinning disc confocal microscopy

Mesh:

Year:  2016        PMID: 27193839      PMCID: PMC5508561          DOI: 10.1007/978-1-4939-3542-0_1

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  9 in total

1.  Spinning disk confocal microscope system for rapid high-resolution, multimode, fluorescence speckle microscopy and green fluorescent protein imaging in living cells.

Authors:  Paul S Maddox; Ben Moree; Julie C Canman; E D Salmon
Journal:  Methods Enzymol       Date:  2003       Impact factor: 1.600

2.  Stable expression of fluorescently tagged proteins for studies of mitosis in mammalian cells.

Authors:  Patricia Wadsworth; Nasser M Rusan; U Serdar Tulu; Carey Fagerstrom
Journal:  Nat Methods       Date:  2005-12       Impact factor: 28.547

3.  The spatial arrangement of chromosomes during prometaphase facilitates spindle assembly.

Authors:  Valentin Magidson; Christopher B O'Connell; Jadranka Lončarek; Raja Paul; Alex Mogilner; Alexey Khodjakov
Journal:  Cell       Date:  2011-08-19       Impact factor: 41.582

Review 4.  Faster fluorescence microscopy: advances in high speed biological imaging.

Authors:  Peter W Winter; Hari Shroff
Journal:  Curr Opin Chem Biol       Date:  2014-05-09       Impact factor: 8.822

5.  BAC TransgeneOmics: a high-throughput method for exploration of protein function in mammals.

Authors:  Ina Poser; Mihail Sarov; James R A Hutchins; Jean-Karim Hériché; Yusuke Toyoda; Andrei Pozniakovsky; Daniela Weigl; Anja Nitzsche; Björn Hegemann; Alexander W Bird; Laurence Pelletier; Ralf Kittler; Sujun Hua; Ronald Naumann; Martina Augsburg; Martina M Sykora; Helmut Hofemeister; Youming Zhang; Kim Nasmyth; Kevin P White; Steffen Dietzel; Karl Mechtler; Richard Durbin; A Francis Stewart; Jan-Michael Peters; Frank Buchholz; Anthony A Hyman
Journal:  Nat Methods       Date:  2008-04-06       Impact factor: 28.547

6.  A cellophane-strip technique for culturing tissue in multipurpose culture chambers.

Authors:  G G ROSE; C M POMERAT; T O SHINDLER; J B TRUNNELL
Journal:  J Biophys Biochem Cytol       Date:  1958-11-25

7.  Centrosome fragments and microtubules are transported asymmetrically away from division plane in anaphase.

Authors:  Nasser M Rusan; Patricia Wadsworth
Journal:  J Cell Biol       Date:  2005-01-03       Impact factor: 10.539

8.  The role of the lissencephaly protein Pac1 during nuclear migration in budding yeast.

Authors:  Wei-Lih Lee; Jessica R Oberle; John A Cooper
Journal:  J Cell Biol       Date:  2003-02-03       Impact factor: 10.539

9.  Improved genome editing in human cell lines using the CRISPR method.

Authors:  Ivan M Munoz; Piotr Szyniarowski; Rachel Toth; John Rouse; Christophe Lachaud
Journal:  PLoS One       Date:  2014-10-10       Impact factor: 3.240

  9 in total

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