EPF-Lausanne/31 July 2008

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(New page: ==Ligation of parts== We digested a few parts yesterday and we ligated them this morning)
 
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==Ligation of parts==
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We digested a few parts yesterday and we ligated them this morning
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[https://2008.igem.org/wiki/index.php?title=EPF-Lausanne/1_August_2008 Next>>]
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===Ligation of parts===
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We digested a few parts yesterday and we ran them through a gel. It turns out that some of them are not correct and were badly digested, so we cannot do any ligation, and we have to run the digestions again, and even grow the DNA again.
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===2 Step PCR===
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<p>
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The 2nd step went well. All 3 worked. We will now be able to use these DNA strands to make our transcription fractors and test on the chips to see where they actualy bind. <br>
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We have to determine the consensus binding region for each to have a starting point. </p>
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===Cell culture ===
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We did again a culture from the igem stock the headquarters send us. We cultured the following biobricks : I14033, I1466, R0071, B0034, B0015, P0140, R0040, E1010, F1610.

Latest revision as of 12:12, 7 August 2008

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Ligation of parts

We digested a few parts yesterday and we ran them through a gel. It turns out that some of them are not correct and were badly digested, so we cannot do any ligation, and we have to run the digestions again, and even grow the DNA again.

2 Step PCR

The 2nd step went well. All 3 worked. We will now be able to use these DNA strands to make our transcription fractors and test on the chips to see where they actualy bind.
We have to determine the consensus binding region for each to have a starting point.

Cell culture

We did again a culture from the igem stock the headquarters send us. We cultured the following biobricks : I14033, I1466, R0071, B0034, B0015, P0140, R0040, E1010, F1610.