Meeting with Gayathri
Date | |
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Department | General |
Description | Pitched the IP idea |
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Type | Meetings |
- Explaining stuff:
- Random forestwhat are our analytes/requirements for them?how are we identifying/killing off the ones that got it wrong
- we need to figure out the parts/biobricks we'll be using
- make a proper presentation
- the challenge for cloning a shorter gene into bacteria is different from that of a longer gene
- give an idea of the timelines
- "we can meet after a proper proposal"
- she'll reply to mail with literature, reviews for genetic circuits
- we can combine multiple of them maybe
- about the 1ml/5ml concentrations, she think it's definitely possible, is tunable,
- prev igem team lead detection system might have proposed it to be tunable
- talk to abhinav masih
- different colonies with negative feedbacks
- namasi, arya ideaflagellar motilityadaptation circuit which resets it to the prev statee coli chemosensory pathwaywhen a ligand binds, the chemosensory mol gets methylated, which in turn switches on a pathway to phosphorylated, which tells it the flagellar motors to switch the directionquorum sensing also works by cross talk with dna bindingreferences on chemosensory systemsadaptation: it gets reset and hence detects a gradientit can only detect a relativephosphorylated protein as a transcription factor to switch on gene expression"two-component systems"
- PhD students
- previous year igem team she cant ask people to do it for us
- She doesnt mind helping out for discussions
- She doesn't want to be primary PI,
- We need to talk to Thomas as we need a departmental decision to let us use lab facilities
- 50% rule, so we need to contact dept
- To source strains, use references, for example, addgene for plasmids
- biobricks,
- you can contact people/authors of the paper, and people are usually open to sharing their strains for academic purposes
- have backups ready in case you get hindered at the stage of finding a strain
- try sticking to e coli