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

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Fig. 1: our L.lactis bacteria, left is GFP and right is a normal look
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The <i>L. lactis</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</i> NZ9000 with pNZ8048g, the gel was split into several parts, and the parts were observed after certain time-spams 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</i> NZ9000 with pNZ8048g seems to be able to survive the polyacrylamide is liquid state and the polymerization process
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Latest revision as of 01:46, 18 October 2014

Figure 3
 
Figure 3: The L. lactis 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 NZ9000 with pNZ8048g, the gel was split into several parts, and the parts were observed after certain time-spams divided over two weeks
 
L. lactis NZ9000 with pNZ8048g seems to be able to survive the polyacrylamide is liquid state and the polymerization process
 
 
 
 

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