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Found 1 matching solution for this experiment
pPICZαB-CalB
J. Lin-Cereghino, Department of Biological Sciences, University
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Plasmids were linearized within the AOX1 promoter with the restriction enzyme Mph1103I, purified with the DNA Clean & Concentrator™-5 (Zymo Research, Irvine, CA) after restriction digestion, and electroporated into competent yJC100 cells. Immediately after electroporation, cells were allowed to recover for 1 h at 30°C in 1ml of 50% 1M sorbitol/ 50% YPD and plated on selective media. Transformants were confirmed by colony PCR as described previously (Thor et al., 2005). |
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Protocol tips |
Plasmids were linearized within the AOX1 promoter with the restriction enzyme Mph1103I, purified with the DNA Clean & Concentrator™-5 (Zymo Research, Irvine, CA) after restriction digestion, and electroporated into competent yJC100 cells. Immediately after electroporation, cells were allowed to recover for 1 h at 30°C in 1ml of 50% 1M sorbitol/ 50% YPD and plated on selective media. Transformants were confirmed by colony PCR as described previously (Thor et al., 2005). |
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