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Found 2 matching solutions for this experiment
pMCO-AOXα-An
Zhongli Cui, Key Laboratory of Agricultural Environmental Microb
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The expression vectors pMCO-AOXα-An (n = 1, 2, 4, or 8) were linearized with Sal I and transformed into P. pastoris GS115 by electroporation. The charging voltage, resistance, and capacitance were 1,500 V, 250 Ω, and 25 μF, respectively. Positive transformants on YPDZ plates were shifted to new YPDZ plates with pre-marked serial numbers and incubated overnight at 30°C. |
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Protocol tips |
The expression vectors pMCO-AOXα-An (n = 1, 2, 4, or 8) were linearized with Sal I and transformed into P. pastoris GS115 by electroporation. The charging voltage, resistance, and capacitance were 1,500 V, 250 Ω, and 25 μF, respectively. Positive transformants on YPDZ plates were shifted to new YPDZ plates with pre-marked serial numbers and incubated overnight at 30°C. |
pPinkα-appA
Jafar Amani, Applied Microbiology Research Center, Baqiyatallah
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Recombinant pPinkα-appA plasmid was linearized by digestion with BspT1 restriction enzyme and it was transformed into P. pastoris GS115 by electroporation (BTX, ECM630 at 1800 V, 200 Ω and 25 µF with 0.2 cm cuvette), following the Invitrogen protocol. After the transformation, the cuvette contents were spread on PAD plates (Pichia Adenine Dropout) and incubated at 30°C for 10 days. As a negative control, the vector of pPinkα-HC was transformed into P. pastoris. |
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Protocol tips |
Recombinant pPinkα-appA plasmid was linearized by digestion with BspT1 restriction enzyme and it was transformed into P. pastoris GS115 by electroporation (BTX, ECM630 at 1800 V, 200 Ω and 25 µF with 0.2 cm cuvette), following the Invitrogen protocol. After the transformation, the cuvette contents were spread on PAD plates (Pichia Adenine Dropout) and incubated at 30°C for 10 days. As a negative control, the vector of pPinkα-HC was transformed into P. pastoris. |
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