Before any lab work related to the project could begin, I had to undergo pipette training in addition to an "initiation rite" of making a buffer. The lab is truly friendly and the members seem to collectively have a genuine interest in my progression as a researcher.
My junior mentor, Yasin Topcu, has occupied the vast majority of the greenhouse for his blossom-end rot (BER) experiments. I will be aiding his projects this summer as well as progressing my own contribution to BER-related knowledge as described in the "Explaining the Project" post. The seedling tray in the bottom left of the picture below is the F2 population of the BGV7900 and BGV793 cross that should show the segregating leaf color.
Later in the week, I made my own PCR buffers and tested them in the "PCR initiation rite". I used PCR to genotype 2 sets of 4 samples at the fas locus. We ran a gel of the PCR products and confirmed that my buffer works. In addition, Yasin taught me how to read a gel so I could confirm that the + & - controls worked as planned; the two remaining samples were heterozygous and wild-type. So far, I am attaining the exact experience I had hoped for from this opportunity. I even got to assist one graduate student with tissue propagation this week!
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