Team:Chiba/Calendar-Home/7 September 2008
From 2008.igem.org
(Difference between revisions)
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<tr> | <tr> | ||
- | <td width="257">Sample No</td> | + | <td width="257">Sample No.</td> |
<td>1,2</td> | <td>1,2</td> | ||
</tr> | </tr> | ||
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:<br> | :<br> | ||
- | :Left side:BBa_R0010 Sample No.1 | + | :Left side:[http://partsregistry.org/Part:BBa_R0010 BBa_R0010] Sample No.1 |
- | :Right side:BBa_R0010 Sample No.2 | + | :Right side:[http://partsregistry.org/Part:BBa_R0010 BBa_R0010] Sample No.2 |
-->(8/9) | -->(8/9) | ||
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</table> | </table> | ||
- | --> | + | -->left at for 3 hours at 37 degrees. |
-->[[Team:Chiba/protocol/ligation/gelex|Gel Extraction]] | -->[[Team:Chiba/protocol/ligation/gelex|Gel Extraction]] |
Revision as of 02:06, 25 October 2008
6 September 2008 <|> 8 September 2008
Contents |
Laboratory work
Team:Input
no work
Team:Communication
-->(6/9) Digestion Test
- Sample DNA 1 : [http://partsregistry.org/Part:BBa_R0010 BBa_R0010](unknown)
- Sample DNA 2 : [http://partsregistry.org/Part:BBa_R0010 BBa_R0010](100ng/μL)
Sample No. | 1,2 |
Sample DNA(μL) | 12 |
PstⅠ(μL) | 0.5 |
SpeⅠ(μL) | 0.5 |
Buffer 2(μL) | 2 |
(×10)BSA(μL) | 2 |
dH2O(μL) | 3 |
TOTAL(μL) | 20 |
- --->Gel Check
Sample left right Sample DNA(μL) 5 5 Loading Dye(μL) 1 1 TOTAL(μL) 6 6
- Left side:[http://partsregistry.org/Part:BBa_R0010 BBa_R0010] Sample No.1
- Right side:[http://partsregistry.org/Part:BBa_R0010 BBa_R0010] Sample No.2
-->(8/9)
Team:Output
Cloning Digestion
- vector:[http://partsregistry.org/Part:BBa_R0040 BBa_R0040]① 75ng/μl
- insert:[http://partsregistry.org/Part:BBa_S03158 BBa_S03158]② 33.6ng/μl
- insert:[http://partsregistry.org/Part:BBa_S03156 BBa_S03156]③ 33.6ng/μl
- insert:[http://partsregistry.org/Part:BBa_S03160 Ba_S03160]④ 38.4ng/μl
- vector:[http://partsregistry.org/Part:BBa_R0010 BBa_R0010]⑤ 100ng/μl
- insert:[http://partsregistry.org/Part:BBa_J52008 BBa_J52008]⑥ 33.6ng/μl
Sample No. ① ② ③ ④ ⑤ ⑥ DNA(digested sample)(μL) 50 54 54 45 14 54 SpeⅠ(μL) 1 0 0 0 1 0 PstⅠ(μL) 0.5 0.5 0.5 0.5 0.5 0.5 XbaⅠ(μL) 0 0.5 0.5 0.5 0 0.5 BSA(x10)(μL) 0.6 7 7 6 2 7 Buffer2(μL) 6 - - - 2 - Buffer3(μL) - 7 7 6 - 7 dH2O(μL) 1.9 1 1 2 0.5 1 TOTAL(μL) 60μl 70μl 70μl 60μl 20μl 70μl -->left at for 3 hours at 37 degrees.
Sample No. ① ② ③ ④ ⑤ ⑥ DNA(digested sample)(μL) 6 10 10 10 4 10 Loading Dye(μL) 2 2 2 2 1 2 dH2O(μL) 4 - - - 1 2 TOTAL(μL) 12 12 12 12 6 12 well 10 7 7 6 5 7 -->DNA purification (①-④,⑥:7μl ⑤:6μl)