Difference between revisions of "Team:ETH Zurich/Notebook/Text"
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Revision as of 13:26, 30 July 2015
06/22/15
- Interlab study:ligation and transformation
- Redo transformation that failed
- Order primers, Antibodies and lactate kits
06/23/15
- Send trafos (bricks and Interlab parts) for sequencing
- FACS training
- Colony PRC for trafos
- Make cryostocks of interlab positive and negative control
- Design and order lldRO versions (incl lacO)
- transform again InterLab ligated constructs (twice each)
06/24/15
- Colony PCR for InterLab constructs
- Send InterLab constructs for sequencing
- Annexin V part : put parts together with backbone
- Amplify lldR from the genome
- Make overnight culture for GFP cells
- Make cryostocks of the 3 constructs (3 replicates)
- Retransform InterLab control I20270?
- Design and order all remaining constructs/primers
06/25/15
- Got labelled annexin
- ON culture for I35104 and the three InterLab promoters (15mL in total) from picked colony
- Run lldR PCR on gel and purify the construct!
- Look into sTRAIL handling (prepare for use)
- GFP competent cells
06/26/15
- Miniprep Of InterLab study
- Digestion of InterLab-purification
- lldP amplification from the genome--> didn't work!
- Amplify INP from the biobrick and purify from gel
- Alliquoting of TRAIL
06/29/15
- Throw away the incorrect parts
- Transform TOP10 and gfp strains for efficiency study
- Measure concentration of fG0008-fG0012
- Ligate InterLab fragments
- InterLab transformation
- Get Omp-8 cells
- TOP10 ON culture
06/30/15
- Make TOP10 cryostock
- Transformation efficiency study
- Colony PCR Interlab
- Interlab sent to sequencing
- Measure conc of lldP
- Transform pSEVA
- Make new LB+CM plates
- Make an ON culture from c13
07/01/15
- Passage cells
- Pick up Omp-8
- Use B0032 (sequenced) for negative control of InterLab
- Make new LB
- Colony PCR
- Send device to sequencing
- Omp-8 ON culture at 25ºC
- pSEVA ON culture
- Competent cells
07/02/15
- Miniprep pSEVA
- Send one sample of pSEVA for sequencing
- Repeat interlab 2 colony PCR (all negative..)
- Depending on sequencing results: throw out or correctly label the cryo tube which is now called p32-1
- Sample resubmitted for sequencing with reverse primer oiG002
- Remake Omp-8 preculture
- Make TBF buffer
07/03/15
- Mammalian cell passaging
- Order oligos
- Amplification of annexinV
- Digestion of pSEVA low copy
- TPR digestion: failed partly
- Digest of InterLab 2
07/06/15
- Digest pSEVA371
- SOC medium
- Gibson assembly annexin
- Plan mammalian experiments with TRAIL
- Transform interlab, annexinV-pSEVA, pSEVA371, pSEVA271
- Overnight culture of Omp-8 at 16°, 25°, 37°
- Digest pSEVA371
07/07/15
- Passage cells
- Asked Tania
- Comment with Margaux the mammalian experiments
- Cryostocks
- Primer design
- Colombia -> protocol sent
- PCR for lldP-lldR
07/08/15
- Make LB-agar and LB-medium
- pSEVA miniprep
- pSEVA digest and purification with miniprep
- Purify lldR-lldP fragments (fridge) (digest the template first)
- PCR for remaining INP-Annexin fragments
- 2% agarose gel for remaining INP-Annexin fragments
- Make ON cultures of all useful BioBrick transformants for cryo stocks
07/09/15
- Start mammalian experiments+ TRAIL
- Shopping list
- Colony PCR annexinV colony
- Competent Omp-8
- Mammalian cell FACS
- Gibson assembly
- Transformation INP-An, lldP-lldR, AnV, p27 and p30
- Make LB
- Preparation of interlab study
07/10/15
- Colony PCR
- Cryostocks (still missing 27 and 30)
- InterLab FACS done!
- Sequencing
- Make ITA buffer
07/13/15
- Compare results: no results
- Colony PCR of lldR-lldP
- GA for lldR-lldP diluted
- pSEVA271 digestion and miniprep
- Preparation of lldR-lldP plates
- After meeting planning of experiments
- ON culture of AnV and INP-AnV
07/14/15
- Cryostock of interlab device 2
- lldR-lldP colony PCR
- Miniprep of ON of AnV and INP-AnV, send to sequence
- TPR re-do
- BioBrick assembly of luxI-term
- Gel-purify all PCR products from monday
- Evening: set up mammalian cells with christian
- pSEVA ON for cryostock
- BB assembly ligations overnight
07/15/15
- Start TRAIL and E Coli mammalian experiments, monitor all day
- Colony PCR for new colonies of AnV
- ON cultures of AnV
- lldR-lldP miniprep
- Redo digest for luxI-term assembly (C0161)
- Transformation of bb-assembled stuff
- Send for sequencing: the "lldR-lldP" plasmid (once with oiG0003 and once with oiG0004)
- Make overnight culture from cryostock of INP-Annexin_2
- ON of GFP cells for co-culture
- Gibson Assemble Plasmids p62-81
- Transformation of gibson assembled plasmids
07/16/15
- Make cultures of BB assembled, colony PCR
- Make cultures of p62-81, colony PCR, make overnight cultures
- Pick up sequencing labes from shop- afternoon (let grow for a long time): miniprep a lot of INP-Annexin, send for sequencing with oiG0004
- Omp-8 transformation efficiency
- Set up mammalian cells and bacteria for lactate experiment
- Mini-prep C0161 and B0012
- Digest C0161 and B0012
- Overnight culture for interlab
07/17/15
- Set up reader plate
- Gibson assembly for lldR w/o lldP
- Transform and plate lldR constructs
- Lactate experiment: change medium at 12:30
- Make cryostocks of all things to sequence (annexin and all assemblies)
- Send all things for sequencing
- Use TOP10 culture for lactate experiment
- Repeat co-culture 14:00-16:00
- Redo digest of C0161 and B0012 (includde test of enzymes)
07/19/15
- Set up overnight cultures of cryos made on friday plus maybe more of each assembly from 0715 plus from assembly on 0717
07/20/15
- Check sequencing results
- Data process: lactate
- Redo digest to test enzymes
- Send stuff to sequence
- New fragments with new fragments
- Make colony PCR
- Throw away stuff from cryostocks
- Make overnight cultures of what is missing: (p72 and p73)
- Plan mammalian experiments to know how many cells we need each day
- Process data (FACS, InterLab and lactate)
- Make o/n cultures for interlab in triplicates
07/21/15
- Early do interlab and InterLab sumitted
- Keep making new fragments with new primers
- If sequencing is correct, make fragments for PL(5)
- Send p72 to sequence
- New fragments: DPN1 digest, gel, purify from gel
- Miniprep stuff
- Continue TPR, ligate and transform
07/22/15
- TRAIL experiment start at 9:00 fro 3T3
- Repeat transformation of lldR and TPR
- Miniprep c44 and c45 and INP-Ann and p72 to have more plasmid
- Sample organisation study
- Colony PCR and make ON culture of lldR andTRP(12_114_34)
- Send 50 for sequencing with different primer
- Miniprep p73 variants for sequencing
- Colony PCR
- TRAIL experiment 15:30-17:00 FACS machine
- Continue TPR assembly
- Digest BioBrick backbone
- Annexin buffer binding made new
- TOP10 ON
07/23/15
- Colony PCR of GFP-INP-Annexin
- Colony PCR of lldR, 12_117, TPR
- Make more LB
- Digestion Annexin- bb--> no band on annexin
- Send TPR for sequencing
- ON culture of AnnexinV and B0012
- Making Competent Top10 cells
07/24/15
- Miniprep annexin
- Digest INP-An, B0012
- Retransform TPR minipreped yesterday
- Amplify TRP to use in assemblies if sequencing is correct
- Send a lot of things for sequencing (lldR, 12_117)
- Do gibson assembly for pl5, transform
07/26/15
- Precultures
07/27/15
- Experiment with Jurkat cells started (lactate)
- Ligation AnV-BB
- Ordered new lldR-lldP plasmid gblocks
- Miniprep ON cultures (TPR and PL(5))
- Send ON cultures (TPR and PL(5))for sequencing