Team:Rice University/Notebook/18 July 2008
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DavidOuyang (Talk | contribs) (New page: *David Ouyang **Miniprep R0040 (ptet) **Digest Amber Suppressor and ptet **Ligate together **Do ARFP mutant quikchange and DPN1 **Transform ARFP and Amber Suppressor supposed) |
StevensonT (Talk | contribs) |
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+ | =Friday, July 18th= | ||
*David Ouyang | *David Ouyang | ||
**Miniprep R0040 (ptet) | **Miniprep R0040 (ptet) | ||
Line 5: | Line 6: | ||
**Do ARFP mutant quikchange and DPN1 | **Do ARFP mutant quikchange and DPN1 | ||
**Transform ARFP and Amber Suppressor supposed | **Transform ARFP and Amber Suppressor supposed | ||
+ | *Taylor Stevenson | ||
+ | *Repeat PCR from yesterday using these primers (NOTE: to view primers download this link and change extension to .doc (word file)[https://static.igem.org/mediawiki/2008/0/0d/Phage_round_1_primers.mov]). | ||
+ | *#tried raising annealing temperature to 58*C | ||
+ | [[Image:20080718.jpg|400px]] | ||
+ | (100bp standard, BleoC PCR product, Stf PCR product,Ligation of yesterdays digested and CIPed PCR primers, 1kb standard) | ||
+ | <BR><BR><BR><BR> | ||
+ | {| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center" | ||
+ | !align="center"|[[Team:Rice_University|Home]] | ||
+ | !align="center"|[[Team:Rice_University/Team|The Team]] | ||
+ | !align="center"|[[Team:Rice_University/Project|The Project]] | ||
+ | !align="center"|[[Team:Rice_University/Parts|Parts Submitted to the Registry]] | ||
+ | !align="center"|[[Team:Rice_University/Modeling|Modeling]] | ||
+ | !align="center"|[[Team:Rice_University/Notebook|Notebook]] | ||
+ | |} |
Revision as of 21:09, 19 July 2008
Friday, July 18th
- David Ouyang
- Miniprep R0040 (ptet)
- Digest Amber Suppressor and ptet
- Ligate together
- Do ARFP mutant quikchange and DPN1
- Transform ARFP and Amber Suppressor supposed
- Taylor Stevenson
- Repeat PCR from yesterday using these primers (NOTE: to view primers download this link and change extension to .doc (word file)[1]).
- tried raising annealing temperature to 58*C
(100bp standard, BleoC PCR product, Stf PCR product,Ligation of yesterdays digested and CIPed PCR primers, 1kb standard)
Home | The Team | The Project | Parts Submitted to the Registry | Modeling | Notebook |
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