Team:TU Munich/Notebook/Protocols

From 2012.igem.org

(Difference between revisions)
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= Methods =
= Methods =
==Molecular Biology Methods==
==Molecular Biology Methods==
-
 
====plasmid DNA isolation from E.coli (miniprep)====
====plasmid DNA isolation from E.coli (miniprep)====
-
''genomic DNA isolation from S.cerevisiae''
+
====genomic DNA isolation from S.cerevisiae''
-
 
+
====measurement of DNA concentration====
-
''measurement of DNA concentration''
+
====sequencing of plasmid DNA====
-
''sequencing of plasmid DNA''
+
====Agarose gel-electrophoesis====
-
 
+
====in vitro modification of DNA====
-
 
+
====Site-Directed Mutagenesis====
-
 
+
====polymerase chain reaction (PCR)====
-
''Agarose gel-electrophoesis''
+
====colony PCR====
-
in vitro modification of DNA
+
====purification of PCR products====
-
 
+
====Dephosphorylation of DNA====
-
 
+
====DNA restriction enzyme digest====
-
 
+
====ligation / cycled ligation====
-
''Site-Directed Mutagenesis''
+
====Oligohybridization of single-stranded DNA====
-
''polymerase chain reaction (PCR)''
+
====gene synthesis====
-
''colony PCR''
+
-
''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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-
====Immunochemical Methods====
 
==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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=Materials=
=Materials=
 +
 +
==Bacteria and yeast strains==
 +
==used Plasmids==
 +
==Reagents==
 +
==Buffer and Solutions==
 +
==Microbial Media==
 +
 +
 +
 +
 +
 +
==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


Contents




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


Materials

Bacteria and yeast strains

used Plasmids

Reagents

Buffer and Solutions

Microbial Media

References: