Team:TU Delft/16 July 2010 content

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(Difference between revisions)
(Characterization of Anderson RBS sequences)
(Characterization of Anderson RBS sequences)
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<h5>Assembly of reference construct & positive control</h5>
<h5>Assembly of reference construct & positive control</h5>
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[https://2010.igem.org/Team:TU_Delft#/blog?blog=15_July_2010 Yesterday's] digestion products of K081005 and I13401 were set for ligation over the weekend.
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[https://2010.igem.org/Team:TU_Delft#/blog?blog=15_July_2010 Yesterday's] digestion products of K081005 and I13401 were set for ligation over the weekend:
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{| style="color:black; background-color:white;" cellpadding="5" cellspacing="0" border="1"
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|'''#'''
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|'''BioBrick'''
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|'''Insert fragment'''
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|'''Recipient plasmid'''
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|'''Final volume'''
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|-
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|1
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|K136011
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|17.5 μL ‘E-K081005-S’
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|4 μL ‘E-pSB1A2-I13401-X’
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|25 μL
 +
|-
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|2
 +
|K136011
 +
|17.5 μL ‘E-K081005-S’
 +
|4 μL ‘E-pSB1A2-I13401-X
 +
|25 μL
 +
|-
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|3
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|Ligation control
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|None
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|4 μL ‘E-pSB1A2-I13401-X
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|25 μL
 +
|}
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To all samples with an end volume of 25μL, 2.5 μL Ligase buffer was added.
The [[Team:TU_Delft/protocols/birnboim_plasmid_isolation|Birnboim method]] was used to isolate J23100 and I13522 (both in pSB1A2) from the o/n 5 mL LB cultures. The following concentrations of plasmid were obtained:
The [[Team:TU_Delft/protocols/birnboim_plasmid_isolation|Birnboim method]] was used to isolate J23100 and I13522 (both in pSB1A2) from the o/n 5 mL LB cultures. The following concentrations of plasmid were obtained:

Revision as of 21:52, 20 July 2010

Contents

Lab work

Ordered DNA + Solvent Tolerance and Hydrocarbon Sensing

The colony PCR of yesterday was put on1% agarose gel

We harvested the 1 mL bacterial cells of possible correct transformations. The pellets were stored at -20 °C. We used 3 mL of the bacterial cells to make -80 °C stocks.

Characterization of Anderson RBS sequences

Fluorescence measurements Attempt #2

Data analysis to follow shortly (good stuff!)

Assembly of reference construct & positive control

Yesterday's digestion products of K081005 and I13401 were set for ligation over the weekend:

# BioBrick Insert fragment Recipient plasmid Final volume
1 K136011 17.5 μL ‘E-K081005-S’ 4 μL ‘E-pSB1A2-I13401-X’ 25 μL
2 K136011 17.5 μL ‘E-K081005-S’ 4 μL ‘E-pSB1A2-I13401-X 25 μL
3 Ligation control None 4 μL ‘E-pSB1A2-I13401-X 25 μL

To all samples with an end volume of 25μL, 2.5 μL Ligase buffer was added.

The Birnboim method was used to isolate J23100 and I13522 (both in pSB1A2) from the o/n 5 mL LB cultures. The following concentrations of plasmid were obtained:

BioBrick Concentration (ng/μL)
J23100 130.7
I13522 106.7