Team:EPF Lausanne/Calendar/30 August 2013

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Sensing <BR>
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<font size = "4"> Sensing-Effector </font> <BR>
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'''Isolation of genomic MG1655 DNA''' <BR>
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''Isolation of genomic MG1655 DNA'' <BR>
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We followed the manufactures instruction from the DNa isolation kit we recieved in order to isolate the genomic DNA. The yields were within the expected Range, from 120ng/ul-300ng/ul.
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-We followed the manufactures instruction from the DNa isolation kit we received in order to isolate the genomic DNA. The yields were within the expected Range, from 120ng/ul-300ng/ul.
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<font size = "4"> Sensing/Nanoparticles </font> <BR>
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''Digestion of nanoparticles'' <BR>
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-We did one more measurement of the solution containing our nanoparticles and MMP2. The result showed that the Nanoparticles were still the same size.
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<BR>- We did a second try for the digestion with MMP2: only with the Tris buffer, but with a higher concentration of MMP2
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<BR>- Three measurements were done for the second try: the nanoparticles got smaller with MMP2, more clearly than during the first try
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Latest revision as of 22:34, 4 October 2013

Taxi.Coli: Smart Drug Delivery iGEM EPFL

Header

Sensing-Effector

Isolation of genomic MG1655 DNA
-We followed the manufactures instruction from the DNa isolation kit we received in order to isolate the genomic DNA. The yields were within the expected Range, from 120ng/ul-300ng/ul.


Sensing/Nanoparticles

Digestion of nanoparticles
-We did one more measurement of the solution containing our nanoparticles and MMP2. The result showed that the Nanoparticles were still the same size.
- We did a second try for the digestion with MMP2: only with the Tris buffer, but with a higher concentration of MMP2
- Three measurements were done for the second try: the nanoparticles got smaller with MMP2, more clearly than during the first try

Wiki Links

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