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Found 2 matching solutions for this experiment
pVT-opti-mdr3
Ina L. Urbatsch, Department of Cell Biology and Biochemistry, an
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Transformation of P. pastoris strain KM71H and expression analysis were as previously described [31], [35]. Selected strains were grown in a BioFlow IV fermentor and the proteins purified as previously described [13] with the following modifications: 10 mM DTT was included during cell breakage in a glass bead beater to fully reduce the proteins, and all buffers for membrane preparation and chromatography were supplemented with 1 mM β-mercaptoethanol and 0.1 mM tris(2-carboxyethyl)phosphine (TCEP) to keep proteins reduced. |
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Protocol tips |
Transformation of P. pastoris strain KM71H and expression analysis were as previously described [31], [35]. Selected strains were grown in a BioFlow IV fermentor and the proteins purified as previously described [13] with the following modifications: 10 mM DTT was included during cell breakage in a glass bead beater to fully reduce the proteins, and all buffers for membrane preparation and chromatography were supplemented with 1 mM β-mercaptoethanol and 0.1 mM tris(2-carboxyethyl)phosphine (TCEP) to keep proteins reduced. |
pVT-mdr3.5
Ina L. Urbatsch, Department of Cell Biology and Biochemistry, an
Upstream tips |
Protocol tips |
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Transformation of P. pastoris strain KM71H and expression analysis were as previously described [31], [35]. Selected strains were grown in a BioFlow IV fermentor and the proteins purified as previously described [13] with the following modifications: 10 mM DTT was included during cell breakage in a glass bead beater to fully reduce the proteins, and all buffers for membrane preparation and chromatography were supplemented with 1 mM β-mercaptoethanol and 0.1 mM tris(2-carboxyethyl)phosphine (TCEP) to keep proteins reduced. |
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Protocol tips |
Transformation of P. pastoris strain KM71H and expression analysis were as previously described [31], [35]. Selected strains were grown in a BioFlow IV fermentor and the proteins purified as previously described [13] with the following modifications: 10 mM DTT was included during cell breakage in a glass bead beater to fully reduce the proteins, and all buffers for membrane preparation and chromatography were supplemented with 1 mM β-mercaptoethanol and 0.1 mM tris(2-carboxyethyl)phosphine (TCEP) to keep proteins reduced. |
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