Drummond:Protocols: Difference between revisions
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*[[Drummond:Pregrowth| Standard conditions for flow cytometer growth rate assay]] | *[[Drummond:Pregrowth| Standard conditions for flow cytometer growth rate assay]] | ||
*[[Drummond:Transformation|High-efficiency yeast transformation]] | *[[Drummond:Transformation|High-efficiency yeast transformation]] | ||
*[[Drummond:DNA Prep|Yeast genomic DNA prep]] | *[[Drummond:DNA Prep|Yeast genomic DNA prep]] (consider the [http://labs.fhcrc.org/gottschling/Yeast%20Protocols/qgprep.html rather rapid yeast genomic DNA prep] instead) | ||
*[[Drummond:Protein Isolation|Isolating total, soluble and insoluble protein fractions]] | *[[Drummond:Protein Isolation|Isolating total, soluble and insoluble protein fractions]] | ||
*[[Drummond:Competent Cells|Making chemically competent <i>E. coli</i> cells]] | *[[Drummond:Competent Cells|Making chemically competent <i>E. coli</i> cells]] | ||
Latest revision as of 07:47, 13 October 2012
Local Protocols
Here are some protocols we use in the lab.
- Chloroform/methanol precipitation of proteins
- Resolving and detecting ubiquitin
- Using paromomycin to alter translation in yeast
- Cell preparation and protocol to view RFP/TFP fluorescence
- Using the Zeiss LSM 510 confocal microscope
- Yeast OD and cell viability model
- Standard conditions for flow cytometer growth rate assay
- High-efficiency yeast transformation
- Yeast genomic DNA prep (consider the rather rapid yeast genomic DNA prep instead)
- Isolating total, soluble and insoluble protein fractions
- Making chemically competent E. coli cells
- Preparing anti-ubiquitin beads
- Periplasmic protein prep from E. coli
Remote Protocols
- Spore enrichment for random-spore analysis (from Rockmill Meth. Enz. 1991)
- Rather rapid yeast genomic DNA prep (Gottschling Lab)
- SDS-PAGE (Szostak Lab)
