G.tigrina Hox gene DthoxC insertion into prokaryote E.coli / (by UNIamCloning)/2011/10/25

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Current revision (17:28, 25 October 2011) (view source)
(Transformation of E.coli competent cells with resuspended GFP and ATF1 DNA)
 
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==Transformation of E.coli competent cells with resuspended GFP and ATF1 DNA==
==Transformation of E.coli competent cells with resuspended GFP and ATF1 DNA==
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* Today we located our GFP and ATF1 Biobrick parts in the proper plates and took samples from each year: (2011, 2010, 2009).  We resuspended the DNA using 15ul H2O and transformed it into 40ul competent cells.  We also created a positive control using a special plasmid that SHOULD, if the transformation went smoothly, grow nicely on the ampicillin plates, as well as a negative control that should NOT grow on the ampicillin plates - (lest the plates are messed up) - but SHOULD grow on the non-antibiotic plates - (lest the transformation killed the cells).   
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Today we located our GFP and ATF1 Biobrick parts in the proper plates and took samples from each year: (2011, 2010, 2009).  We resuspended the DNA using 15ul H2O and transformed it into 40ul competent cells.  We also created a positive control using a special plasmid that SHOULD, if the transformation went smoothly, grow nicely on the ampicillin plates, as well as a negative control that should NOT grow on the ampicillin plates - (lest the plates are messed up) - but SHOULD grow on the non-antibiotic plates - (lest the transformation killed the cells).   
After adding 950ul - (from the protocol... next time, only add 200ul!) - SOC NP to the tubes of resuspended DNA and competent cells, we allowed them to "shake" - (mix) - for 60 minutes.  Then, we spread the GFP and ATF1 mixes and our two controls onto ampicillin plates, and our negative control and leftover competent cells onto non-antibiotic plates, and placed them into the oven at 37°C overnight.
After adding 950ul - (from the protocol... next time, only add 200ul!) - SOC NP to the tubes of resuspended DNA and competent cells, we allowed them to "shake" - (mix) - for 60 minutes.  Then, we spread the GFP and ATF1 mixes and our two controls onto ampicillin plates, and our negative control and leftover competent cells onto non-antibiotic plates, and placed them into the oven at 37°C overnight.

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Transformation of E.coli competent cells with resuspended GFP and ATF1 DNA

Today we located our GFP and ATF1 Biobrick parts in the proper plates and took samples from each year: (2011, 2010, 2009). We resuspended the DNA using 15ul H2O and transformed it into 40ul competent cells. We also created a positive control using a special plasmid that SHOULD, if the transformation went smoothly, grow nicely on the ampicillin plates, as well as a negative control that should NOT grow on the ampicillin plates - (lest the plates are messed up) - but SHOULD grow on the non-antibiotic plates - (lest the transformation killed the cells). After adding 950ul - (from the protocol... next time, only add 200ul!) - SOC NP to the tubes of resuspended DNA and competent cells, we allowed them to "shake" - (mix) - for 60 minutes. Then, we spread the GFP and ATF1 mixes and our two controls onto ampicillin plates, and our negative control and leftover competent cells onto non-antibiotic plates, and placed them into the oven at 37°C overnight.


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