Team:UNITN-Trento/Notebook/Labposts/07/57

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Revision as of 07:55, 9 September 2013

{ "date" : "2013-07-11", "author" : "gabriele", "title" : "Extraction (again) and ligation", "content" : "

SAM synthetase extraction

Last time I determined the correct protocol to extract SAM synthetase from the E. coli using the new plasmid (at the end, the protocol was the usual one). I performed three PCRs (G1, G2, G3) and run the products on 1% agarose gel.
Gel
Loading scheme
1kb ladderG1G2G3
\"Gel\"


Ligation

At first, I added 1µl of SAP to pSB1C3 O/N digestion and 1µl of DpnI to SAMsynthetase O/N digestion, and incubated the samples at 37°C for 1.5h. Then I quantified the digestions.
SampleQuantity
SAM synthetase12.2ng/µl
pSB1C314.0ng/µl

Then I performed the ligation and left the reaction run for 2h at room temperature.
Ligation Mixes
CTRL1:11:2
Buffer4µl
Plasmid14.29µl
Insert09.15µl18.3µl
Ligase1µl
Water20.71µl11.56µl2.41µl
Then I transformed the ligation products in NEB10β", "tags" : "SAMsynthetase" }