Team:Groningen/Template/MODULE/Notebook/bandage/week7

From 2014.igem.org

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Our L.lactis bacteria, seen through a phase contrast microscope (every white dot is GFP)
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The <i>L. lactis bacteria</i> NZ9000 with pNZ8048g, seen through a phase contrast microscope, on the right the GFP channel is displayed
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18 August - 22 August
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August 18 - August 22
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repeated the same process as the week before. Poured the gel again, with cells from an overnight culture.
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Pouring a polyacrylamide gel with an overnight culture of <i>L. lactis bacteria</i> NZ9000 with pNZ8048g, the gel was plit into several parts, and the parts were observed after certain timespams divided over two weeks
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We've split this gel in several parts where we will check one of these parts in two weeks.
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Induction still seems to work fine, our lactis seems to survives the poisenous acrylamid and a temperature of over 80 °C.
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<i>L. lactis bacteria</i> NZ9000 with pNZ8048g seems to be able to survive the polyacrylamide is liquid state and the polymerization process
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Revision as of 01:45, 18 October 2014

Figure 3
 
Figure 3: The L. lactis bacteria NZ9000 with pNZ8048g, seen through a phase contrast microscope, on the right the GFP channel is displayed
 
 
August 18 - August 22
 
Pouring a polyacrylamide gel with an overnight culture of L. lactis bacteria NZ9000 with pNZ8048g, the gel was plit into several parts, and the parts were observed after certain timespams divided over two weeks
 
L. lactis bacteria NZ9000 with pNZ8048g seems to be able to survive the polyacrylamide is liquid state and the polymerization process
 
 
 
 

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