No discussions found
Start your discussion
Share your thoughts or question with experts in your field
Start a discussion
Found 5 matching solutions for this experiment
pD912
Robert Speight, Queensland University of Technology, Brisbane, Q
Upstream tips |
Protocol tips |
Downstream tips |
|
P. pastoris cells were transformed following a condensed standard protocol (58). The amounts of DNA used were adjusted depending on the vector size (see Results). After the transformation, screenings and rescreenings of the indicated numbers of transformants (Fig. 2 and and3)3) were performed as outlined previously (13, 28, 30). |
|
Protocol tips |
P. pastoris cells were transformed following a condensed standard protocol (58). The amounts of DNA used were adjusted depending on the vector size (see Results). After the transformation, screenings and rescreenings of the indicated numbers of transformants (Fig. 2 and and3)3) were performed as outlined previously (13, 28, 30). |
P_AOX1Syn
"Anton Glieder, Institute of Molecular Biotechnology, Graz Unive
Upstream tips |
Protocol tips |
Downstream tips |
|
Each plasmid was amplified in E. coli, linearized with BglII or SmiI (Fermentas) and transformed into the corresponding P. pastoris strains. Single colonies were transferred to 96-well deep-well plates for standard cultivation as described previously [42]. To compare the expression levels, GFP fluorescence was measured as described by [47]. |
|
Protocol tips |
Each plasmid was amplified in E. coli, linearized with BglII or SmiI (Fermentas) and transformed into the corresponding P. pastoris strains. Single colonies were transferred to 96-well deep-well plates for standard cultivation as described previously [42]. To compare the expression levels, GFP fluorescence was measured as described by [47]. |
P_GAP
"Anton Glieder, Institute of Molecular Biotechnology, Graz Unive
Upstream tips |
Protocol tips |
Downstream tips |
|
Each plasmid was amplified in E. coli, linearized with BglII or SmiI (Fermentas) and transformed into the corresponding P. pastoris strains. Single colonies were transferred to 96-well deep-well plates for standard cultivation as described previously [42]. To compare the expression levels, GFP fluorescence was measured as described by [47]. |
|
Protocol tips |
Each plasmid was amplified in E. coli, linearized with BglII or SmiI (Fermentas) and transformed into the corresponding P. pastoris strains. Single colonies were transferred to 96-well deep-well plates for standard cultivation as described previously [42]. To compare the expression levels, GFP fluorescence was measured as described by [47]. |
pPuzzle-eGFP
Diethard Mattanovich, Austrian Centre of Industrial Biotechnolog
Upstream tips |
Protocol tips |
Downstream tips |
|
Plasmids were linearized within the genome integration region prior to electroporation (2 kV, 4 ms, GenePulser, BioRad) into electrocompetent P. pastoris. Multicopy integration of HSA expressing clones was done as described by Marx et al. [19] and selected at higher Zeocin concentrations (up to 1000 μg mL-1). |
|
Protocol tips |
Plasmids were linearized within the genome integration region prior to electroporation (2 kV, 4 ms, GenePulser, BioRad) into electrocompetent P. pastoris. Multicopy integration of HSA expressing clones was done as described by Marx et al. [19] and selected at higher Zeocin concentrations (up to 1000 μg mL-1). |
pPuzzle
Brigitte Gasser, Department of Biotechnology, BOKU, University o
Upstream tips |
Protocol tips |
Downstream tips |
|
After digestion with AscI and BspHI the transformation of the P. pastoris wild type strain X-33 was performed by electroporation. The repressible promoter cassette should interact with the genomic DNA in the cell and replace the respective promoter of the gene of interest (Figure 4B) [15]. |
|
Protocol tips |
After digestion with AscI and BspHI the transformation of the P. pastoris wild type strain X-33 was performed by electroporation. The repressible promoter cassette should interact with the genomic DNA in the cell and replace the respective promoter of the gene of interest (Figure 4B) [15]. |
Can't find the product you've used to perform this experiment? It would be great if you can help us by
Adding a product!