Team:Groningen/4 October 2010

From 2010.igem.org

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{{Team:Groningen/Header}}
{{Team:Groningen/Header}}
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'''Week 29'''
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'''Week 40'''
'''Expression'''-''Peter and David''
'''Expression'''-''Peter and David''
A expression experiment was performed to get samples for the mass spectometry.
A expression experiment was performed to get samples for the mass spectometry.
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<br>
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Strain E and deltaTasA were grown in TY over night. The next morning OD was measured and both strains were diluted in fresh TY with antibiotics in 100 mL and divided into dTasA, E and E non induced.
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OD was measured every hour, at approximately OD = 0,5 (after 2,5 hours) 1% subtilin was addded to the E-culture and from then onward every 2 hours OD was measured.
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After five hours the OD was measured again and samples were taken for preperation:
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The following groups were prepared out of 2 mL of culture:
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E/dTasA/EN pellet
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E/dTasA/EN pellet, SDS
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E/dTasA/EN pellet, Lysozyme
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E/dTasA/EN pellet, Lysozyme SDS
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E/dTasA/EN supernatant
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E/dTasA/EN supernatant, SDS
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E/dTasA/EN supernatant, Lysozyme
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E/dTasA/EN supernatant, Lysozyme SDS
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 +
Samples were stored in the freezer to await further analysis using mass spec.
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'''Week 41'''
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<br>
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'''Week 43'''
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<br>
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'''Expression experiment David & Peter'''
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<br>
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Massspec data for the induced cultures of E, EN, C and CN was aquired, with the help of Sander we performed Malditov mass spectometry on both these samples and the samples in stock from the large E induction experiment. The samples of the E-induction experiment gave no data.
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<br>
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[[Image:MassSpecGR.jpg]]
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<br>
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<br>
'''Laura'''
'''Laura'''
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Expanding gene expression model and programmed this in Matlab, searched for constants.
Expanding gene expression model and programmed this in Matlab, searched for constants.
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'''Arend'''
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Information standard ready for submission
{{Team:Groningen/Footer}}
{{Team:Groningen/Footer}}

Latest revision as of 02:22, 28 October 2010

iGEM Groningen 2010

Hydrophobofilm
pushing coatings into a greener future

Week 40

Expression-Peter and David

A expression experiment was performed to get samples for the mass spectometry.
Strain E and deltaTasA were grown in TY over night. The next morning OD was measured and both strains were diluted in fresh TY with antibiotics in 100 mL and divided into dTasA, E and E non induced.

OD was measured every hour, at approximately OD = 0,5 (after 2,5 hours) 1% subtilin was addded to the E-culture and from then onward every 2 hours OD was measured.

After five hours the OD was measured again and samples were taken for preperation:

The following groups were prepared out of 2 mL of culture:

E/dTasA/EN pellet E/dTasA/EN pellet, SDS E/dTasA/EN pellet, Lysozyme E/dTasA/EN pellet, Lysozyme SDS

E/dTasA/EN supernatant E/dTasA/EN supernatant, SDS E/dTasA/EN supernatant, Lysozyme E/dTasA/EN supernatant, Lysozyme SDS

Samples were stored in the freezer to await further analysis using mass spec.

Week 41



Week 43


Expression experiment David & Peter


Massspec data for the induced cultures of E, EN, C and CN was aquired, with the help of Sander we performed Malditov mass spectometry on both these samples and the samples in stock from the large E induction experiment. The samples of the E-induction experiment gave no data.


MassSpecGR.jpg



Laura

Expanding gene expression model and programmed this in Matlab, searched for constants.

Arend Information standard ready for submission

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