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Team:Panama/27 July 2010
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(New page: {{:Team:Panama/Header2}} ==='''July 27'''=== ''Miniprep'' Today we performed the miniprep of the E. coli transformed with the RBS and Promoter parts. This miniprep was made in triplicate...) |
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==='''July 27'''=== | ==='''July 27'''=== | ||
| - | ''Miniprep'' | + | |
| - | Today we performed the miniprep of the E. coli transformed with the RBS and Promoter parts. This miniprep was made in triplicate. | + | == ''Miniprep'' == |
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| + | Today we did the minipreps of the cultures that we grew for 16 hours yesterday. | ||
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| + | Today we performed the miniprep of the ''E. coli'' transformed with the RBS and Promoter parts. This miniprep was made in triplicate. | ||
''Electrophoresis'' | ''Electrophoresis'' | ||
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| + | After the miniprep we made an electrophoresis in 1% agarose gel with 1X TBE buffer. Also, we measured the DNA concentration with a spectrophotometer: | ||
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| - | + | [[Image:Cuadro27julio.jpg|400px|thumb|left|alt text]] | |
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| - | + | [[Image:GEL27JULIO.JPG|350px|thumb|left|alt text]] | |
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| + | '''NOTE:''' From here on end, when we see 1 and 2 for the samples, we mean that the second one is a duplicate. | ||
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| + | Expected size | ||
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| + | RBS=2092 bp | ||
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| + | Promoter=2103 bp | ||
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| + | Reporter=2800 bp | ||
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| + | Spectrometer measurement | ||
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| + | [RBS]=30,4 ηg/μl | ||
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| + | ''Digestion'' | ||
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| + | After the DNA concentration measurement, we performed the digestion of the RBS and Promoter parts. | ||
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| + | These quantities of reaction materials were used for both the RBS and the Promoter Reactions: | ||
| + | [[Image:Untitled6.jpg|200px|thumb|left|alt text]] | ||
{{:Team:Panama/calendar2}} | {{:Team:Panama/calendar2}} | ||
Latest revision as of 03:39, 27 October 2010
July 27
Miniprep
Today we did the minipreps of the cultures that we grew for 16 hours yesterday.
Today we performed the miniprep of the E. coli transformed with the RBS and Promoter parts. This miniprep was made in triplicate.
Electrophoresis
After the miniprep we made an electrophoresis in 1% agarose gel with 1X TBE buffer. Also, we measured the DNA concentration with a spectrophotometer:
NOTE: From here on end, when we see 1 and 2 for the samples, we mean that the second one is a duplicate.
Expected size
RBS=2092 bp
Promoter=2103 bp
Reporter=2800 bp
Spectrometer measurement
[RBS]=30,4 ηg/μl
Digestion
After the DNA concentration measurement, we performed the digestion of the RBS and Promoter parts.
These quantities of reaction materials were used for both the RBS and the Promoter Reactions:
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