Virginia Commonwealth/27 July 2009
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+ | {| class="wikitable" border=".5" alignment="center" | ||
+ | |+For Digestion and Ligation of Promoters | ||
+ | |- | ||
+ | !##!!A260!!Volume (uL)!!Concentration (ug/uL)!!Amount (ug) | ||
+ | |- | ||
+ | |pSB4C5||.086||19.5||.172||3.18 | ||
+ | |- | ||
+ | |J06702||.023||125.0||.040||5.75 | ||
+ | |- | ||
+ | |BBa_J23101||.052||35.2||.104||3.66 | ||
+ | |} | ||
+ | |||
+ | ''Maria and Afton'' | ||
+ | * Nothing is glowing except one colony, J23110 w/ 702 | ||
+ | [[User:Trentay|Trentay]] 16:57, 28 July 2009 (UTC) | ||
---- | ---- | ||
+ | |||
===Tasks=== | ===Tasks=== | ||
+ | ''Kevin & Adam'' | ||
+ | *Discuss and continue to study design principles for T7 and various other inducible/repressible promoters. | ||
+ | |||
+ | ''Maria and Afton'' | ||
+ | * Regrow, Miniprep, Take spectrophotometry measurements, Digest, Ligate, Transform ligated parts: | ||
+ | ** pSB4C5, J23110, J06702, | ||
+ | * Troubleshoot and Repeat this process until RFP is expressed | ||
+ | * Make overnight cultures of parts pSB4C5, J23110, J06702, J23110 w/ 702 | ||
+ | [[User:Trentay|Trentay]] 16:57, 28 July 2009 (UTC) | ||
---- | ---- | ||
- | |||
- | |||
====Wetlab==== | ====Wetlab==== | ||
- | *1 | + | ''Kevin & Adam'' |
- | * | + | *Digest and Ligate synthetic promoter designs 1-9. |
+ | |||
+ | ''Maria and Afton'' | ||
+ | * Overnight cultures were made (5mL of selective broth with 100 microliters of DNA) | ||
+ | ** Samples taken from cryogenic stocks | ||
+ | *** J23110 (AMP) | ||
+ | *** J06702 (AMP) | ||
+ | *** pSB4C5 (Cm) | ||
+ | ** Samples taken from plates | ||
+ | *** J23110 w/ 702 | ||
+ | [[User:Trentay|Trentay]] 16:57, 28 July 2009 (UTC) |
Latest revision as of 16:57, 28 July 2009
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Contents |
Monday 27 July 2009
Results
Kevin & Adam
## | A260 | Volume (uL) | Concentration (ug/uL) | Amount (ug) |
---|---|---|---|---|
Design 1 0.0 | .017 | 40.1 | .034 | 1.36 |
Design 1 0.5 | .018 | 40.1 | .036 | 1.44 |
Design 1 1.0 | .014 | 40.0 | .028 | 1.12 |
Design 1 1.5 | .012 | 40.4 | .024 | .97 |
Design 2 | .047 | 39.4 | .094 | 3.7 |
Design 3 | .028 | 41.0 | .056 | 2.29 |
Design 4 | .039 | 48.0 | .078 | 3.74 |
Design 5 | .032 | 36.0 | .064 | 2.30 |
Design 6 | .030 | 39.7 | .060 | 2.38 |
Design 7 | .029 | 43.0 | .058 | 2.49 |
Design 8 | .022 | 39.2 | .044 | 1.72 |
Design 9 | .032 | 41.9 | .064 | 2.68 |
## | A260 | Volume (uL) | Concentration (ug/uL) | Amount (ug) |
---|---|---|---|---|
pSB4C5 | .086 | 19.5 | .172 | 3.18 |
J06702 | .023 | 125.0 | .040 | 5.75 |
BBa_J23101 | .052 | 35.2 | .104 | 3.66 |
Maria and Afton
- Nothing is glowing except one colony, J23110 w/ 702
Trentay 16:57, 28 July 2009 (UTC)
Tasks
Kevin & Adam
- Discuss and continue to study design principles for T7 and various other inducible/repressible promoters.
Maria and Afton
- Regrow, Miniprep, Take spectrophotometry measurements, Digest, Ligate, Transform ligated parts:
- pSB4C5, J23110, J06702,
- Troubleshoot and Repeat this process until RFP is expressed
- Make overnight cultures of parts pSB4C5, J23110, J06702, J23110 w/ 702
Trentay 16:57, 28 July 2009 (UTC)
Wetlab
Kevin & Adam
- Digest and Ligate synthetic promoter designs 1-9.
Maria and Afton
- Overnight cultures were made (5mL of selective broth with 100 microliters of DNA)
- Samples taken from cryogenic stocks
- J23110 (AMP)
- J06702 (AMP)
- pSB4C5 (Cm)
- Samples taken from plates
- J23110 w/ 702
- Samples taken from cryogenic stocks
Trentay 16:57, 28 July 2009 (UTC)