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CAROL
Verification of amplification of luxCDABE from polymerase chain reaction (PCR)
- Prepared 0.7% Agarose gel
- Used orange G dye
- Ran gel at 90V for 90 minutes
RESULTS:
- From the results, there is contamination in the negative control, but it did amplify the 6KB LUXCDABE. The large bands is a result of loading too much DNA.
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CHINMOYEE
CLASS
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EMILY
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FAHD
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IMAN
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JAMIE
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JEREMY
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KATIE
Planning PCR Activity
Started to make an outline of what I will be required to do for PCR machine:
- Need some way to add items to the machine to make it more interactive then just telling the machine what is required
- Looked through the lsl wiki and found llAllowInventoryDrop, which is a function that seems to allow for addition of objects to another as long as it is set to true
- If anything can be added then I need to have a way to get rid of everything that is added
- I will need some way to incorporate other information besides materials, such as temperatures and times for each cycle
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KEVIN
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MANDY
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PATRICK
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PRIMA
Marketing
Today, I continued my follow-ups with companies via email. Jeremy, Vicki and I wrote up Thank You letters to the Dragons from Dragon's Den for taking the time out of their busy schedules to watch our marketing pitches, provide feedback, advising us on marketing and business initiatives and way to sell our project.
I researched a few more companies that I had found, wrote up emails and updated the Gmail marketing document.
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STEFAN
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VICKI
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