Team:Calgary/17 August 2009
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- | + | Colony PCR and Marketing | |
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- | + | It turns out that I had used the Low-melt agarose on Friday to make my 1% gel. Unfortunately, the gel didn't turn out well and I had to postpone my work to Monday. Today, I made a 1% gel with the normal agarose powder and remade my stock (3 microL PCR product, 2 microL dye & 15 microL ddH2O) and ran my gel at 100V. | |
+ | The results showed exactly what I was expecting. Since I had used regular BBK CP primers and length of my construct was 885bp, the total length of the bands should've been 1135bp. My bands were just above the 1kb ladder band! I let the students visiting our lab make my overnight cultures. Tomorrow, I'll do a mini-prep and a restriction digest to verify the size of my construct. If all else is good, I'll send it to sequencing. | ||
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+ | I followed up with the T-shirt company but unfortunately I couldn't get a hold of her. I'll follow up tomorrow. I also called numerous new companies and sent our sponsorship package to one of them. I left a voice mail for the rest of the companies. I'll follow up with them tomorrow. I also began write-ups for the August newsletter. | ||
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Revision as of 22:44, 17 August 2009
UNIVERSITY OF CALGARY