Team:TU Munich/Notebook/Protocols
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= Methods = | = Methods = | ||
==Molecular Biology Methods== | ==Molecular Biology Methods== | ||
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====plasmid DNA isolation from E.coli (miniprep)==== | ====plasmid DNA isolation from E.coli (miniprep)==== | ||
- | + | ====genomic DNA isolation from S.cerevisiae'' | |
- | + | ====measurement of DNA concentration==== | |
- | + | ====sequencing of plasmid DNA==== | |
- | + | ====Agarose gel-electrophoesis==== | |
- | + | ====in vitro modification of DNA==== | |
- | + | ====Site-Directed Mutagenesis==== | |
- | + | ====polymerase chain reaction (PCR)==== | |
- | + | ====colony PCR==== | |
- | in vitro modification of DNA | + | ====purification of PCR products==== |
- | + | ====Dephosphorylation of DNA==== | |
- | + | ====DNA restriction enzyme digest==== | |
- | + | ====ligation / cycled ligation==== | |
- | + | ====Oligohybridization of single-stranded DNA==== | |
- | + | ====gene synthesis==== | |
- | + | ||
- | + | ||
- | + | ||
- | + | ||
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==Crude protein extraction from S.cerevisiae== | ==Crude protein extraction from S.cerevisiae== | ||
==SDS-Polyacrylamid-Gelelektrophoresis (SDS-PAGE)== | ==SDS-Polyacrylamid-Gelelektrophoresis (SDS-PAGE)== | ||
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==Western Blot== | ==Western Blot== | ||
====Microbiological Methods==== | ====Microbiological Methods==== | ||
- | ==cultivation of ''E.coli''== | + | ====cultivation of ''E.coli''==== |
- | ==cultivation of ''S.cerevisiae''== | + | ====cultivation of ''S.cerevisiae''==== |
- | ==heat shock transformation of ''E.coli'' with plasmid DNA== | + | ====heat shock transformation of ''E.coli'' with plasmid DNA==== |
- | == transformation of ''S.cerevisiae''== | + | ====transformation of ''S.cerevisiae''==== |
- | ==genome integration== | + | ====genome integration==== |
+ | |||
+ | |||
+ | |||
====Chemical Methods==== | ====Chemical Methods==== | ||
==Phycocyanobilin (PCB) extraction from dried Spirulina platensis powder== | ==Phycocyanobilin (PCB) extraction from dried Spirulina platensis powder== | ||
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??? | ??? | ||
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=Materials= | =Materials= | ||
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+ | ==Bacteria and yeast strains== | ||
+ | ==used Plasmids== | ||
+ | ==Reagents== | ||
+ | ==Buffer and Solutions== | ||
+ | ==Microbial Media== | ||
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+ | ==References:== | ||
+ | *[http://www.ncbi.nlm.nih.gov/pubmed/20010584 '''Pubmed:''' Prasher, 1995: Using GFP to see the light.(Review)] |
Revision as of 10:11, 13 September 2012
Methods
Molecular Biology Methods
plasmid DNA isolation from E.coli (miniprep)
====genomic DNA isolation from S.cerevisiae
measurement of DNA concentration
sequencing of plasmid DNA
Agarose gel-electrophoesis
in vitro modification of DNA
Site-Directed Mutagenesis
polymerase chain reaction (PCR)
colony PCR
purification of PCR products
Dephosphorylation of DNA
DNA restriction enzyme digest
ligation / cycled ligation
Oligohybridization of single-stranded DNA
gene synthesis
Protein biochemical methods
Protein expression in S.cerevisiae
Crude protein extraction from S.cerevisiae
SDS-Polyacrylamid-Gelelektrophoresis (SDS-PAGE)
Western Blot
Microbiological Methods
cultivation of E.coli
cultivation of S.cerevisiae
heat shock transformation of E.coli with plasmid DNA
transformation of S.cerevisiae
genome integration
Chemical Methods
Phycocyanobilin (PCB) extraction from dried Spirulina platensis powder
??? • Introducing new Saccharomyces cerevisiae strain (Y190 strain) from Schwab lab for Y2H o Aim of the experiment: The Y190 Saccharomyces cerevisiae is a special strain for Yeast-two-hybrid. This strain carries a Gal4 and Gal80 deletion to higher the signal/noise-ratio of protein-protein interactions. Reporter for protein-protein interactions are HIS3, lacZ and MEL1 and are encoded in the genomic DNA. Transformation markers are trp1, leu2 and cyhR2 and are encoded on the transformation plasmids. • Gradient PCR • Cycled ligation • Inoculation of YPD medium with S. cerevisiae and brewing yeast strain 34/70 (part 2/3) o Aim of the experiment: Discrimination of growing ability in wort medium. • Electroporation of electrocompetent E. coli with P698+699