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Capitoli
- 00:05Titolo
- 02:03Haploid Cell Growth
- 03:08Conducting a Cross
- 04:43Harvesting Preparations
- 05:57Flow Cytometry
- 09:01Preparation for DeltaVision Microscopy
- 11:05Representative Analysis of Zygote Purification
- 14:27Conclusion
To purify zygotes of S. cerevisiae, haploid cells of opposite mating type were engineered to express red or green fluorescent proteins, co-incubated to allow zygote formation, and fractionated using a flow cytometry-based protocol. The highly-enriched fraction enables subsequent "-omic" studies, recovery of initial progeny, and systematic investigation of zygote morphogenesis.
Tags
Flow Cytometry-based PurificationS. Cerevisiae ZygotesHaploid CellsDiploid StatesMating TypeStable DiploidsMitotic DivisionsZygote FormationSoluble Mating FactorsReceptor-mediated Signaling CascadesCell-cell FusionModel For Progenitor Or Stem Cell FunctionBiochemistry Of Zygote FormationPurification Of Yeast ZygotesSedimentation PropertiesHypertonic Sorbitol
