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| protocols-sops 2010/11/24 21:16 | protocols-sops 2010/11/24 21:20 current | ||
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| ====== Protocols-Standard operating Procedures (SOP) ====== | ====== Protocols-Standard operating Procedures (SOP) ====== | ||
| - | ===== Plasmid DNA isolation_ alkaline lysis mini prep | + | ===== Plasmid DNA isolation_ alkaline lysis mini prep ===== |
| - | ===== | + | |
| Modified from: Sambrook & Russell 2001, Kirchhof 2002 | Modified from: Sambrook & Russell 2001, Kirchhof 2002 | ||
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| Materials & Reagents | Materials & Reagents | ||
| Alkaline lysis solution I: 50mM glucose, 25mM Tris-Cl pH 8.0, 10mM EDTA pH 8.0 | Alkaline lysis solution I: 50mM glucose, 25mM Tris-Cl pH 8.0, 10mM EDTA pH 8.0 | ||
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| Alkaline lysis solution II: 0.2N NaOH, 1% SDS; make fresh | Alkaline lysis solution II: 0.2N NaOH, 1% SDS; make fresh | ||
| Alkaline lysis solution III: 60ml 5M potassium acetate, 11.5ml glacial acetic acid, 28.5ml ddH2O; place on ice before use | Alkaline lysis solution III: 60ml 5M potassium acetate, 11.5ml glacial acetic acid, 28.5ml ddH2O; place on ice before use | ||
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| 3M Sodium acetate (pH 5.2) | 3M Sodium acetate (pH 5.2) | ||
| TE buffer: 10mM Tris-Cl pH 8.0, 1mM EDTA pH 8.0 | TE buffer: 10mM Tris-Cl pH 8.0, 1mM EDTA pH 8.0 | ||
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| Protocol | Protocol | ||
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| ===== DNA quantification_ using Spectrophotometer ===== | ===== DNA quantification_ using Spectrophotometer ===== | ||
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| Materials & Reagents | Materials & Reagents | ||
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