From 2009.igem.org
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- | Descriptive Title of What You're Doing
| + | Colony PCR of J13002 + JuxOD47A BBk + B0015 on pSB1AK3 that I prepared yesterday |
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- | WIKI CODING HERE
| + | Purpose: The bacterial culture growth is prolific. This will verify if the proper gene constructs are included within. |
| + | |
| + | Materials an methods: |
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| + | * Primers: BBk forward and reverse construction primers |
| + | * Master mix: Use pTaq DNA polymerase. The contents will suffice for 15 tubes, and were prepared in the same fashion as on June 26. |
| + | * PCR conditions: These are also the same as they were on June 26 |
| + | |
| + | Results: |
| + | |
| + | The 1% agarose gel is attached below. Lane 1 is a GeneElute 1kb+ DNA ladder; lanes 2-11 are the colony-PCR'd samples of J13002 + LuxOD47A + B0015; lane 12 is a sequenced LuxOD47A + B0015 for a size control; lane 13 is a sequenced LuxOD47A BBk for another size control; and lane 14 is a negative control. Based on a very confusing negative control, this procedure will be repeated tomorrow. We will still progress with a NotI restriction digest of the contents, which will also be done tomorrow. |
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Revision as of 23:30, 20 August 2009
University of Calgary
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CAROL
Descriptive Title of What You’re Doing
WIKI CODING HERE
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CHINMOYEE
Descriptive Title of What You're Doing
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EMILY
Descriptive Title of What You're Doing
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FAHD
Descriptive Title of What You're Doing
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IMAN
Descriptive Title of What You're Doing
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JAMIE
Descriptive Title of What You're Doing
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JEREMY
Descriptive Title of What You're Doing
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KATIE
Descriptive Title of What You're Doing
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KEVIN
Other hyperactive antifreeze proteins
- High Arctic plant rhizosphere(P. putida)
- Mid-gut of frozen beetle larvae (R. erythropolis)
- Frozen/chilled pork sausages (M. cryophilus)
- Antarctic soil (Moraxella sp and P. fluorescens).
None were from bacteria until MpAFP was found
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MANDY
Descriptive Title of What You're Doing
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PATRICK
Descriptive Title of What You're Doing
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PRIMA
Descriptive Title of What You're Doing
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STEFAN
Descriptive Title of What You're Doing
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VICKI
Colony PCR of J13002 + JuxOD47A BBk + B0015 on pSB1AK3 that I prepared yesterday
Purpose: The bacterial culture growth is prolific. This will verify if the proper gene constructs are included within.
Materials an methods:
- Primers: BBk forward and reverse construction primers
- Master mix: Use pTaq DNA polymerase. The contents will suffice for 15 tubes, and were prepared in the same fashion as on June 26.
- PCR conditions: These are also the same as they were on June 26
Results:
The 1% agarose gel is attached below. Lane 1 is a GeneElute 1kb+ DNA ladder; lanes 2-11 are the colony-PCR'd samples of J13002 + LuxOD47A + B0015; lane 12 is a sequenced LuxOD47A + B0015 for a size control; lane 13 is a sequenced LuxOD47A BBk for another size control; and lane 14 is a negative control. Based on a very confusing negative control, this procedure will be repeated tomorrow. We will still progress with a NotI restriction digest of the contents, which will also be done tomorrow.
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