User:Behzad Damadzadeh/Notebook/PcTF Subcloning in E-coli/2013/01/24
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NLS-6His-STOP-F1 CTAGAcccaagaaaaagcgcaaggtacaccatcaccaccatcacgcgtaaagctgagACTAGTAGCGGCCGCTGCA 76 | NLS-6His-STOP-F1 CTAGAcccaagaaaaagcgcaaggtacaccatcaccaccatcacgcgtaaagctgagACTAGTAGCGGCCGCTGCA 76 | ||
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NLS-6His-STOP-R1 GCGGCCGCTACTAGTctcagctttacgcgtgatggtggtgatggtgtaccttgcgctttttcttgggT 68 | NLS-6His-STOP-R1 GCGGCCGCTACTAGTctcagctttacgcgtgatggtggtgatggtgtaccttgcgctttttcttgggT 68 | ||
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Heat at 100°C for 5 min., remove the entire heat block or water bath from the heat source, and allow to cool slowly to room temperature.<br> | Heat at 100°C for 5 min., remove the entire heat block or water bath from the heat source, and allow to cool slowly to room temperature.<br> | ||
--> *10x annealing buffer: 1 M NaCl; 100 mM Tris-HCl, pH 7.4 | --> *10x annealing buffer: 1 M NaCl; 100 mM Tris-HCl, pH 7.4 | ||
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| + | Ligation of NLS-HIS-STOP and V0120 vector in DH5α-T and BL21 | ||
| + | * V0120 cut with X/P and purified from the gel. | ||
| + | * Ligations | ||
| + | {| {{table}} cellspacing="3" <!-- Ligations table --> | ||
| + | |- bgcolor=#cfcfcf | ||
| + | | Ligation || <font color="blue"><u></font> | ||
| + | |- | ||
| + | | 1. E. coli DH5α-T NLS-HIS-STOP/size, 20 ng +V0120 (X/P)/3200, 14.1ng || <font color="blue">KNLS-HIS-STOP/C-His 3:1 No Colonies</font> | ||
| + | |- | ||
| + | | 2. E. coli BL-21 NLS-HIS-STOP/size, 16 ng + V0120 (X/P)/3200, 14.1ng || <font color="blue">NLS-HIS-STOP/C-His 3:1 No Colonies</font> | ||
| + | |- | ||
| + | | 3. E. coli BL-21 NLS-HIS-STOP/size, 22.8 ng + V0120 (X/P)/3200, 14.1ng || <font color="blue">NLS-HIS-STOP/C-His 2:1 No Colonies</font> | ||
| + | |- | ||
| + | | 4. E. coli BL-21 NLS-HIS-STOP/size, 20 ng + V0120 (X/P)/3200, 14.1ng || <font color="blue">NLS-HIS-STOP/C-His 3:1 </font> | ||
| + | |- | ||
| + | | 5. V0120 (X/P)/3200)/ 15 ng (Control Plate)|| | ||
| + | |} | ||
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| + | * Calculations are for the ng of insert we need to get a 3:1 ratio of insert molecules to 50 ng vector molecules | ||
| + | {| {{table}} cellspacing="3" <!-- Ligation rxn table --> | ||
| + | | || 1 || 2 || 3 || 4 || 5 | ||
| + | |- | ||
| + | | Insert DNA || 2.34 || 2.34 || 2.05 || 2.05 || --- | ||
| + | |- | ||
| + | | Vector DNA || 1.92 || 1.92 || 1.92 || 1.92 || 1.92 | ||
| + | |- | ||
| + | | 2x lgn buf (Roche) || 5.26 || 5.26 || 5.0 || 5.0 || 5.0 | ||
| + | |- | ||
| + | | T4 ligase (NEB) || 1.0 || 1.0 || 1.0 || 1.0 || 1.0 | ||
| + | |- | ||
| + | | dH<sub>2</sub>O || 0 || 0 || 0.03 || 0.03 || 2.08 | ||
| + | |- | ||
| + | | || 10.52 μL || 10.52 μL || 10μl || 10μL || 10μL | ||
| + | |} | ||
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| + | * The incubation time for the ligation process was 30min at room temperature. | ||
| + | * Fast transformation, 30 min on ice. | ||
Revision as of 16:39, 25 January 2013
Main project page Previous entry Next entry
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01/24/2013'Making Standardized DNA Part (NLS-HIS-STOP)' NLS-6His-STOP-F1 CTAGAcccaagaaaaagcgcaaggtacaccatcaccaccatcacgcgtaaagctgagACTAGTAGCGGCCGCTGCA 76 NLS-6His-STOP-R1 GCGGCCGCTACTAGTctcagctttacgcgtgatggtggtgatggtgtaccttgcgctttttcttgggT 68 Set up an annealing reaction as follows:
Heat at 100°C for 5 min., remove the entire heat block or water bath from the heat source, and allow to cool slowly to room temperature.
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