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Single-step Marker Switching in Schizosaccharomyces pombe Using a Lithium Acetate Transformation Protocol

Authors: Simon David Brown
Simon David BrownAffiliation: Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK
Bio-protocol author page: a3916
 and Alexander Lorenz
Alexander LorenzAffiliation: Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK
For correspondence: a.lorenz@abdn.ac.uk
Bio-protocol author page: a3917
date: 12/20/2016, 1321 views, 0 Q&A
DOI: https://doi.org/10.21769/BioProtoc.2075.

[Abstract] The ability to utilize different selectable markers for tagging or mutating multiple genes in Schizosaccharomyces pombe is hampered by the historical use of only two selectable markers, ura4+ and kanMX6; the latter conferring resistance to the antibiotic G418 (geneticin). More markers have been described ...

Chromatin Fractionation Assay in Fission Yeast

Authors: Tatsuki Kunoh
Tatsuki KunohAffiliation: Graduate School of Natural Science and Technology, Okayama University, Okayama, Japan
For correspondence: tkunoh06@gmail.com
Bio-protocol author page: a1508
 and Toshiyuki Habu
Toshiyuki HabuAffiliation: Radiation Biology Center, Kyoto University, Kyoto, Japan
Bio-protocol author page: a1509
date: 7/20/2014, 3144 views, 0 Q&A
DOI: https://doi.org/10.21769/BioProtoc.1185.

[Abstract] The protein recruitment onto chromatin is a critical process for DNA metabolism, including DNA replication, DNA repair and DNA recombination. Especially DNA modification enzymes and checkpoint proteins are loaded onto DNA damage sites in a context-dependent manner. In our recent study (Kunoh and Habu, ...

Fluorescence Recovery After Photobleaching (FRAP) in the Fission Yeast Nucleus

Authors: Petrina Delivani
Petrina DelivaniAffiliation: Department of Molecular Cell Biology and Genetics, Max Planck Institute, Dresden, Germany
For correspondence: delivani@mpi-cbg.de
Bio-protocol author page: a914
Mariola R. Chacón
Mariola R. ChacónAffiliation: Department of Molecular Cell Biology and Genetics, Max Planck Institute, Dresden, Germany
For correspondence: mchacon@mpi-cbg.de
Bio-protocol author page: a915
Britta Schroth-Diez
Britta Schroth-DiezAffiliation: Department of Molecular Cell Biology and Genetics, Max Planck Institute, Dresden, Germany
For correspondence: schroth@mpi-cbg.de
Bio-protocol author page: a916
 and Iva M. Tolić-Nørrelykke
Iva M. Tolić-NørrelykkeAffiliation: Department of Molecular Cell Biology and Genetics, Max Planck Institute, Dresden, Germany
For correspondence: tolic@mpi-cbg.de
Bio-protocol author page: a493
date: 10/20/2013, 3864 views, 0 Q&A
DOI: https://doi.org/10.21769/BioProtoc.941.

[Abstract] We use fluorescence recovery after photobleaching (FRAP) to calculate the diffusion coefficient of GFP in the nucleoplasm of fission yeast. The FRAP method can be generally used to measure the mobility of proteins inside the cell or its organelles.
In our experiment we only measured the diffusion of ...
1 

Fluorescence Recovery After Photobleaching (FRAP) in the Fission Yeast Nucleus

Authors: Petrina Delivani
Petrina DelivaniAffiliation: Department of Molecular Cell Biology and Genetics, Max Planck Institute, Dresden, Germany
For correspondence: delivani@mpi-cbg.de
Bio-protocol author page: a914
Mariola R. Chacón
Mariola R. ChacónAffiliation: Department of Molecular Cell Biology and Genetics, Max Planck Institute, Dresden, Germany
For correspondence: mchacon@mpi-cbg.de
Bio-protocol author page: a915
Britta Schroth-Diez
Britta Schroth-DiezAffiliation: Department of Molecular Cell Biology and Genetics, Max Planck Institute, Dresden, Germany
For correspondence: schroth@mpi-cbg.de
Bio-protocol author page: a916
 and Iva M. Tolić-Nørrelykke
Iva M. Tolić-NørrelykkeAffiliation: Department of Molecular Cell Biology and Genetics, Max Planck Institute, Dresden, Germany
For correspondence: tolic@mpi-cbg.de
Bio-protocol author page: a493
date: 10/20/2013, 3864 views, 0 Q&A
DOI: https://doi.org/10.21769/BioProtoc.941.

[Abstract] We use fluorescence recovery after photobleaching (FRAP) to calculate the diffusion coefficient of GFP in the nucleoplasm of fission yeast. The FRAP method can be generally used to measure the mobility of proteins inside the cell or its organelles.
In our experiment we only measured the diffusion of ...

Chromatin Fractionation Assay in Fission Yeast

Authors: Tatsuki Kunoh
Tatsuki KunohAffiliation: Graduate School of Natural Science and Technology, Okayama University, Okayama, Japan
For correspondence: tkunoh06@gmail.com
Bio-protocol author page: a1508
 and Toshiyuki Habu
Toshiyuki HabuAffiliation: Radiation Biology Center, Kyoto University, Kyoto, Japan
Bio-protocol author page: a1509
date: 7/20/2014, 3144 views, 0 Q&A
DOI: https://doi.org/10.21769/BioProtoc.1185.

[Abstract] The protein recruitment onto chromatin is a critical process for DNA metabolism, including DNA replication, DNA repair and DNA recombination. Especially DNA modification enzymes and checkpoint proteins are loaded onto DNA damage sites in a context-dependent manner. In our recent study (Kunoh and Habu, ...

Single-step Marker Switching in Schizosaccharomyces pombe Using a Lithium Acetate Transformation Protocol

Authors: Simon David Brown
Simon David BrownAffiliation: Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK
Bio-protocol author page: a3916
 and Alexander Lorenz
Alexander LorenzAffiliation: Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK
For correspondence: a.lorenz@abdn.ac.uk
Bio-protocol author page: a3917
date: 12/20/2016, 1321 views, 0 Q&A
DOI: https://doi.org/10.21769/BioProtoc.2075.

[Abstract] The ability to utilize different selectable markers for tagging or mutating multiple genes in Schizosaccharomyces pombe is hampered by the historical use of only two selectable markers, ura4+ and kanMX6; the latter conferring resistance to the antibiotic G418 (geneticin). More markers have been described ...
1 
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