NYMU Taipei/Lab Notes/2007 10 4
From 2007.igem.org
(Difference between revisions)
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<tr><td>10X buffer</td><td>2 uL</td></tr> | <tr><td>10X buffer</td><td>2 uL</td></tr> | ||
<tr><td>T4 ligase</td><td>1 uL</td></tr> | <tr><td>T4 ligase</td><td>1 uL</td></tr> | ||
- | <tr><td | + | <tr><td>insert:vector</td><td>1:7</td></tr> |
</table> | </table> | ||
</td> | </td> | ||
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<tr><td>10X buffer</td><td>2 uL</td></tr> | <tr><td>10X buffer</td><td>2 uL</td></tr> | ||
<tr><td>T4 ligase</td><td>1 uL</td></tr> | <tr><td>T4 ligase</td><td>1 uL</td></tr> | ||
- | <tr><td | + | <tr><td>insert:vector</td><td>1:5.5</td></tr> |
</table> | </table> | ||
</td> | </td> | ||
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<tr><td>10X buffer</td><td>2 uL</td></tr> | <tr><td>10X buffer</td><td>2 uL</td></tr> | ||
<tr><td>T4 ligase</td><td>1 uL</td></tr> | <tr><td>T4 ligase</td><td>1 uL</td></tr> | ||
- | <tr><td | + | <tr><td>insert:vector</td><td>1:7</td></tr> |
</table> | </table> | ||
</td> | </td> |
Revision as of 15:04, 4 October 2007
digestion check of CinR+HSL+D-term,pCinRHSL and pOmpC (vectors)
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- after gel separation, their O.D. was checked. However, it is too low
Re-check the concentration of inserts and vectors
ligation setup
- criteria
- make vector have around 100 ng in sample (total volume 20 uL)
- maximize the insert volume, and insert is larger than vector
ligation I: pCinRHSL (vector) + OmpRBS (insert) | ligation II: pOmpC (vector) + TATA_INSA (insert) | ligation III: CinR+HSL+D-term (vector) + TATB_INSB (insert) | ||||||||||||||||||||||||||||||
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