Lab Aug 29, 2009

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(New page: We need to do as many assemblies as we can today, but in between the digestion and ligation steps we need to run a gel to confirm presence of all the parts. We need to pick several (4-7) c...)
 
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We need to do as many assemblies as we can today, but in between the digestion and ligation steps we need to run a gel to confirm presence of all the parts. We need to pick several (4-7) colonies from each successful plate of composite parts that was transformed on the 27th. We need to start nanospec-ing our plasmids once prepped so we can tell if DNA concentration is a limiting factor. Finally we need to deal with out p1010-kan. It looks like there should be colonies of our newly rehydrated backbone when we come in tomorrow if we are lucky.
We need to do as many assemblies as we can today, but in between the digestion and ligation steps we need to run a gel to confirm presence of all the parts. We need to pick several (4-7) colonies from each successful plate of composite parts that was transformed on the 27th. We need to start nanospec-ing our plasmids once prepped so we can tell if DNA concentration is a limiting factor. Finally we need to deal with out p1010-kan. It looks like there should be colonies of our newly rehydrated backbone when we come in tomorrow if we are lucky.
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Latest revision as of 22:16, 17 October 2009

We need to do as many assemblies as we can today, but in between the digestion and ligation steps we need to run a gel to confirm presence of all the parts. We need to pick several (4-7) colonies from each successful plate of composite parts that was transformed on the 27th. We need to start nanospec-ing our plasmids once prepped so we can tell if DNA concentration is a limiting factor. Finally we need to deal with out p1010-kan. It looks like there should be colonies of our newly rehydrated backbone when we come in tomorrow if we are lucky.



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