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Team:University of Lethbridge/Notebook/Project3October
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===October 14 2008=== | ===October 14 2008=== | ||
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Ran a gel of gel exraction products to determine presence/quantity of DNA. | Ran a gel of gel exraction products to determine presence/quantity of DNA. | ||
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Band close to ~150 bp for the +18 rpsA DNA, which is approximately the correct size. | Band close to ~150 bp for the +18 rpsA DNA, which is approximately the correct size. | ||
No band present for the +1 TIR DNA, meaning gel extraction was not successful. | No band present for the +1 TIR DNA, meaning gel extraction was not successful. | ||
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===October 16 2008=== | ===October 16 2008=== | ||
Revision as of 01:13, 28 October 2008
Back to The University of Lethbridge Main Notebook
Contents |
October 7 2008
Andrew
Ran a gel to confirm presence of DNA from PCR on September 30 2008. DNA present in all wells, so a 2% agaraose gel was prepared for a gel extraction of DNA. 40uL of DNA was loaded to be extracted.
October 14 2008
Andrew, Nathan Puhl
Ran a gel of gel exraction products to determine presence/quantity of DNA.
Band close to ~150 bp for the +18 rpsA DNA, which is approximately the correct size. No band present for the +1 TIR DNA, meaning gel extraction was not successful.
October 16 2008
Andrew
Ligation of +18 rpsA DNA into pGEM TEZ beacuse primer design requires DNA to be in a plasmid for endonuclease activity of restriction enzymes.
Heat deactivated at 65 C after 1 hour incubation at 37 C.
October 21 2008
Andrew
Transformation of +18 rpsA TIR DNA into pGEM TEZ to make enough DNA to be restricted/ligated into biobrick format. (psB1A2)
50 uL og xgal added to LB + amp plates to screen for blue and white colonies.
October 22 2008
Andrew
Transformation into pGEM TEZ successful, many white and some blue colonie on both plates.
Picked 3 colonies from each plate to grow in 5mL LB + amp for a pDNA prep.
October 23 2008
Andrew
pDNA prep of 6 culture tubes using a kit
