Team:Johns Hopkins/Notebook/Vio

From 2011.igem.org

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'''Procedure''':
'''Procedure''':
* See [[File:Miniprep stet prep pm .pdf|Meluh Lab Protocol]] for boiling mini prep.
* See [[File:Miniprep stet prep pm .pdf|Meluh Lab Protocol]] for boiling mini prep.
-
* [[File:June 10 restiction digest rxn mixes.jpg|See Double Digest Reaction Mixes here]]
+
* [[File:June 10 restiction digest rxn mixes.jpg|thumb|300px|See Double Digest Reaction Mixes here]]
** All other parts (promoters and UTR's) double digested with XmaI and SphI)
** All other parts (promoters and UTR's) double digested with XmaI and SphI)
* See neb.com for correct digestion procedures with each enzyme.   
* See neb.com for correct digestion procedures with each enzyme.   

Revision as of 03:00, 27 September 2011

VitaYeast - Johns Hopkins University, iGEM 2011

Related Links:
Notebook: Other Yeast Toolkit:
Promoters and UTRs
Violacein

Violacein loxPsym Integration
June 7th, 2011

Purpose:

  1. Make 4 copies of violacein building blocks and select promoters and 3’UTRs on 96 well plates. 2 were made previously by Dr. Boeke's Lab Tech and I (not entered into wiki). Therefore I am only making 2 new copies today.
  2. Begin growing colonies on petri dishes (to prepare for miniprep).

Procedure:

  • Made 100ml LB+Carbenicillin Solution (ampicillin resistance gene also resists Carbenicillin) using 100uL 1000x Carbenicillin (thawed from -20 degrees Celsius) and 100mL LB Broth.
  • Labelled plates and Petri Dishes
    • Except for one petri dish (forgot to add a label), each label says: “iGEM: Boeke promoter, 3’ end & Vio BB’s from YW (pseudonym); F2.”
  • Transferred LB+Carb solution to a ‘sterile reagent reservoir for multi-channel pipetting.
  • Took out a previous copy of the genes (arrayed on a 96 well plate) from -80 degree freezer, placed in a centrifuge with a balance.
    • Centrifuged until speed reached 1000g (short spin).
  • Used a 12-lane multichannel micropipette to transfer 100uL of LB+Carb to rows A-D on new 96 well plates.
  • Placed air-pore tape on each new 96 well plate (now inoculated) and incubated them at 37 degrees Celsius.
    • Incubated petri dishes at 37 degrees.

Problems:

  • I added LB+carb to every well in rows a-d. The original array only filled row A/C, half of row B and 11/12 wells in Row D.
    • Always remember how original array was organized and always stick to it.
  • Original plate (the one being copied) was left out for around 50min. Not good.
    • Next time, only take out plate from -80 after each new 96 well plate/petri dish has been prepared for inoculation (e.g. LB+Carb should be added to wells before original plate is taken out to thaw).
  • I am still learning where everything in the lab is. This will take time.
  • When pipetting, I would scrape the tip onto the side of the well to get rid of the final drops. This motion resulted in me almost mixing the original cultures.
    • Remember: Do not worry about “pipetting the last drop.”
  • When inoculating petri dishes, the liquid sprayed out of the tip instead of dripping out.
    • Don’t let the liquid spray out of the tip, the different cultures may mix.
June 9th, 2011

Purpose:

  • Inoculated test tubes (filled with ~ 5mL LB+Carb)with each part (Vio ORF Building Blocks (ie ORF fragments), Promoters and UTR's)

Procedure:

  • For each part, took wooden stick, placed flat end onto a single colony on the agar plate, dipped stick into the appropriate text tube (inoculating the test tube) and threw out the stick.
  • Incubated them overnight at 37 degrees on a shaker (a slanted spinning wheel with slots for test tubes).
June 10th, 2011

Purpose:

  • Mini-Prep of parts (Vio ORF Building Blocks, Promoters, UTR's)
  • Double Cut Restriction Digest of Mini Prep Samples (to run an analytical gel to check if the correct inserts (parts) are present).

Procedure:

  • See File:Miniprep stet prep pm .pdf for boiling mini prep.
  • See Double Digest Reaction Mixes here
    • All other parts (promoters and UTR's) double digested with XmaI and SphI)
  • See neb.com for correct digestion procedures with each enzyme.
  • After digestions completed, stored samples at -20 degrees Celsius.


Results:

June 10 mini prep.jpg

Results show high concentrations of plasmid, too high. In reality there is RNA in the solution too and nanodrop detects nucleic acid without distinction for DNA or RNA. According to Dr. Boeke’s Lab Tech, the readings still indicate that the DNA concentration is probably high.

Problems:

Mini Prep:
  • Instead of boiling all 29 samples at once, I boiled 15 and then 14. For the first 15, I boiled for 2min 45sec and not the required 3 minutes. The reason: the water was not boiling when we entered the samples. At the last minute, we had to refill the bath with hot water and place the samples in. We set the timer for 4 minutes and the water started to boil with 2minutes 45seconds left.
  • Sometimes during mini prep, I did not change the tip for each sample while aspirating supernatant.
June 11th, 2011

Purpose:

  • Gel Electrophoresis of Yesterday's Digests

Procedure:

  • Added 4uL CS Red Dye (with added RNAse) to each sample and 2 log ladder.

Problems:

  • Added 7uL Dye to VioA2
  • Ladder Didn't show up on the gel (must redo tomorrow).


June 13th, 2011

Purpose:

  • Redo Digest (No image uploaded), the ladders on the gel did not show up. Will use 2 log ladder with blue Juice this time and not CS Red. Will add a second digest condition for VioE, using a BsaI single cut.
    • Note: Although the ladder couldn't be seen properly, we agreed that the patterns/digests were correct and matched what we expected. We believe there is nothing wrong with our restriction enzymes or our starting material (parts).

Procedure:

  • See reaction here
  • See neb.com for correct digestion procedures.


Problems:

  • Accidentally heated VioE2 tube with the others at 37 degrees. After 37 degree heating, I Placed it in 50 degree water bath for around 1hour 55minutes. Made a PCR tube of new VioE2 solution (according to above table) and used thermocycler (PCR machine) to heat it for 2hours at 65 degrees and refrigerate it (4 degrees) afterwards). Still not the right temperature. I made yet another PCR tube of VioE2 (VioE2=VioE cut with BsaI) and 'PCR'd' at 50 degrees (I refer to this tube now as 'VioE BsaI cut (3).'
  • "R" from Zhu lab took VioD BB’s and VioE2 out for me and placed the samples in my minus 20 freezer space. I left the lab when I put them to digest.


June 14th, 2011

Purpose:

  • Run a preparative gel (a gel for gel extraction/purification of Vio ORF Building Blocks).

Procedure:

  • Made 200uL of 1% agarose gel with 1x Ethidium Bromide (diluted from 20000x) added.
    • 25 thick lanes indented into gel.
  • Planned Lanes:

20110614 planned lanes.jpg

      • Note: Lane 25 for this run was for VioE BsaI Cut (3) (see June 13th's 'Problems' section).

Results:

  • Gel looked fine. Got expected band patterns. See todays 'Problems' section

Problems:

  • Projects:20110614 gel extraction 1.jpg?linkonly
    • It's not good practice to take a picture of a gel before gel extraction, UV exposure can damage the DNA. Hand held UV light can go to long wave, unlike the 'picture taker, which uses only short wave UV light' Long form is less harmful to the DNA. This gel must be re-done.
    • Note: New practice is to allow pictures before gel extraction, but exposure to short wave UV light must be as short as possible (less than a split second is good).
  • See 'Blooper' section. As we exposed the gel (today's image on the wiki) for a short time to short UV, we could have used it for gel extraction. Unfortunately, it fell and shattered.
  • I redid the digests according to the June 13th protocol to run a future analytic gel (to definitively see if the patterns are what we expect).
    • Note: I also ran another exact set of digests in parallel for a future preparative gel for gel extraction.


June 15th, 2011

Purpose:

  • Run an analytical gel to determine if the digests worked before we do a preparative gel.

Procedure:

  • Made 2x 200mL 1% gels with EB, exactly like the June 14th Gel.
  • Made a 100mL gel with 25 thick, narrow lanes. We decided that we should use a smaller gel for an analytical gel. This way (out of 1 tube of 25uL digest mixture + CS Red) we can load 3uL for the analytical gel and the rest for the preparative gel. I originally made a copy of each digest; one for analytical, one for preparative. We decided to use one copy for both (the second set of digests I made remain unused).
  • 2 log ladder in lane 2, 100bp ladder in lane 24.
  • Problem:
  • Accidentally switched the 2nd copy Vio B BB1 (which should have remained unused) with the first copy of VioB BB2 (which should have been loaded). It was a mis-labelling error. There are 2 vio B BB1 samples in the analytical gel (lanes 5 and 7), and no VioB BB2. We decided we could proceed to the preparative gel step as I found the 1st copy VioB BB2.


June 19th, 2011

Purpose:

  • Plan with Zheng how to do a ligation reaction (I planned today to digest the vector in preparation for the gel extraction and future ligation of ORF buidling blocks).
  • Final Planned Procedure for Ligation:
  • Projects:ashan ligation rxn mix.jpg?linkonly
    • Note: If using enzymatics reagents, ligate at room temp for an hour. If NEB reagents, 16 degrees Celsius (from now on, all temperature measurements are in Celsius) overnight.


June 20th, 2011

Purpose: Gel Extraction

Procedure: See Qiagen Gel Purification protocol, June 13th Gel Specifics

  • Only 16uL VioE 2x RE Cut loaded into the gel.
  • 120V 15min, 10V 15min, 130V 10 Min (all to try and separate 2 bands, only 1 of which we wanted to extract.
  • Left for home after QG, NaAcetate and 100% Isopropanol were added to the excised gel fragments (experiment not finished yet). A post-doc said this is OK to do.


June 21st, 2011

Purpose:

  • Finish gel purification

Results:

  • DNA concentrations are small, but workable. I digested 30uL of each ORF with 1uL of each enzyme and added dye just in case.


June 22nd, 2011

Purpose:

  • Just came in to add dye to the VioD digests (they need to be digested at 2 temps, which is why I didn't add dye to them with the others).



June 30th, 2011

Purpose:

  • Replica Plate transformed colonies from LB+Carb plates to LB+Carb+XGal+IPTG Plates.

Procedure:

  • Mixed 3ml LB with 500uL 1000x IPTG and 500uL 1000x XGal.
    • Spread 19X200uL aliquots of this solution onto 19 LB+Carb Plates using sterile glass beads.
    • Note: I selected 15 out of 31 plates for replica plating and made 4 extra Xgal plates just in case.
  • Dr. Boeke said to let transformed colonies grow more at 37 degrees.
  • Left the 15 selected plates in the 37 degree incubator, left the new xgal plates to soak on my bench, placed all other plates in the 4 degree fridge.

Problems:

  • Wasted lots of time thawing the xgal because its solvent is DMSO and I left it on ice to thaw. Note: Never leave DMSO on ice to thaw, it will not melt. Do not even leave thawed DMSO on ice, it will refreeze quickly.
  • Be more careful when pouring beads, wasted a couple.
July 1st, 2011

Purpose:

  • Replica Plate transformed colonies from LB+Carb plates to LB+Carb+XGal+IPTG Plates (made yesterday).
  • Inoculate glass tubes for mini prep for each white colony on the xgal destination plates.

Procedure:

  • Drew a line on original plate and destination plate. Used it to make sure destination plate colonies had the same orientation as original plate. Looked for white colonies in the evening.
  • Pressed original plate onto a sterile velvet, pressed empty destination plate onto the newly 'dirty' velvet to pick up the colonies.
  • Filled glass tubes with 5mL LB+5uL Carb, labeled them according to ligation condition (16 degree or room temp incubation), transformation volume (e.g. 180uL transformation mixture added to the plate) & sample name (e.g. VioA, VioB,...VioE).
  • For all white colonies on the destination plates, I found the colony location on the destination plate and picked it with a wooden stick(pressed the flat end onto the colony, avoiding small satellite colonies). I then shook the picked colony in the LB mixture vigorously, threw the toothpick, and placed the tubes in a 37 degree shaking incubator overnight.
July 2nd, 2011

Purpose:

  • Miniprep from yesterday's inoculated tubes.
  • Digest

Procedure:

July 3rd, 2011

Purpose:

  • Run an analytical get to see if the correct inserts are present.

Procedure:

  • Prepare a 200mL 1% agarose gel with EB and 25 think lanes.
  • Add 10uL of digest and CS red dye.
  • Run at 150V and take picture after 40min.

Results:

July 5th, 2011

Purpose:

  • Make 14 replica plates of A/B

Procedure:

  • Used 25mL of agar, 25uL of IPTG and Xgal, and 150mL LB
  • Mix consists of 375uL of Xgal, 375uL of IPTG, and 2250uL of LB for a total volume of 3000uL.
  • 30, 90, and R 30uL plates held at 16 degrees Celsius.

Results:

  • VioA and VioE 30uL RT had no colonies.
  • Because the original colonies were very small, the 90uL B was not re-plated to allow it to grow more.
  • All colonies incubated at 30 degrees Celsius to try to lower the amount of Halos.
  • Note: Halos: Original colony secretes resistance protein for other colonies to leech off of. Only good colonies survive in liquid suspension, as Halos can't effectively leech anymore. Streaking on a new plate kills most Halos too.
July 6th, 2011

Purpose:

  • Find whites on replica plate B-90 1b and inoculate the white on the A XGal plate
  • June 27th ligation: aliquot 5uL and save, leave the rest overnight.
  • Transformation (June 27th protocol)
  • Protocol:
  • Transform dilute PTE 19 after first A/B tubes heat shocked.
  • Put ligation tubes back to 16 degrees Celsius after heat shock of vector and negative control.

Results:

  • One plate of A-30-RT has a white-ish colony (Placed in 37 degrees Celsius to see if it turns blue
  • All useless inoculated plates from yesterday thrown out (except the whitish A, which was put in 4 degrees Celsius).
  • No DNA control full of bacteria
  • PTE19 plate empty
  • PTE-LB plate chalk full
  • Conclusion: No DNA plate and PTE19 plate (LB-Carb) switched. No DNA bacteria went to PTE19 plate and vice-versa. PTE cannot be toxic as it grows on LB.
July 7th, 2011
  • Protocol:
  • Inoculate from July 5th VioB (85uL, 45uL at 16 degrees Celsius) and July 30th VioA (180uL at 16 degrees Celsius)
  • Replica plate July 6th VioA (30-90-180 at 16 degrees Celsius)
  • PTE19 plate in 4 degrees Celsius and negative DNA and PTE LB (proof)

Results:

  • "All whitish A" from yesterday was blue...not using it.
  • July 5th 15uL VioB had ambiguous large colonies, want to let it grow
July 8th, 2011

Purpose:

  • Miniprep B-T 16-285 a, B-T 16-245 & A 16 180 (Take 3mL of each and split into 2 1.5mL tubes)

Procedure:

  • Aided STET suspension by heating at 37 degrees Celsius for 5min
  • After double digest, run 100mL 1% agarose gel with EB for 25min
  • Inoculate relica whites if gel doesn't work
  • Vortexed B-T456 and A minipreps before adding to digest mix
  • Run 50mL 1% agarose gel with EB for 25min at 150V

- Lanes: Ladder, A, B-45, B-85, Ladder

Results:

  • Inoculated B-T 16-285 b and c were clear, with no bacteria
  • 15uL VioB had no colonies
  • VioA 185 and B 95 had one white colony each
  • Gel broke, but probably still worked
  • Gel Pic: Lab:20110708 ligation analytic gel a b .jpg?linkonly
  • Dr. Boeke suggests digesting with the middle restriction enzyme (for the unique restriction site that stitched the BBs together)to make sure to make competent cells, design primers to add BSAI sites and unique sequences for each Vio expression cassette objective, and stitch all cassettes to the neochromosome in one go.
  • Suggestions: Whenever measuring pieces, always digest the vector alone and run it alongside the others. Also, run gels longer, add EB to TE.
July 9th, 2011

Purpose:

  • Make sure no internal BsaI or BsnbI sites are in any designs.
  • Double digest within regions (no E required, at least 3 Bs)
  • Single digest with BsaI
  • Choose the more plentiful Eu out of XmaI and SphI
  • Design primers according to the incoming Boeke diagram
July 10th, 2011

Procedure:

  • Run gel at 150V for 1 hour (500mL, 1% agarose)
  • Lanes: Ladder, A B C D (BsaI), A B B2 B3 C D, Ladder
  • Add 400mL TE and and EB

Results:

July 11th, 2011

Purpose:

  • Make 500uL of CS red dye with 0.1ug/uL of RNAse
  • Digests
July 12th, 2011

Purpose:

  • Run gel at 150V for 75min (1% agarose with EB in gel and buffer, 5uL CS red dye per sample)
  • design Boeke oligos
  • Protocol:
  • Lanes: Ladder, BsaI A B B B, Ladder, BsaI C C D D, Ladder

Results:

July 13th, 2011

Purpose:

  • Run 50mL 1% agarose gel with EB (300mL TTE & 15uL EB for 45min at 150V)

Results:

  • VioB is not here :( Transform overnight ligations, miniprep and try again
July 19th, 2011

Purpose:

  • Digest and ligate B 1, 2, 3 to PTZ19u tomorrow
  • Transform overnight ligations
  • Design oligos
July 23th, 2011

Purpose:

  • Ligations
  • Finish oligos with Boeke

Procedure:

  • Cooked vector at 65 degrees Celsius for 20min

Results:

  • Will aliquot 6uL for transformations. Leave rest overnight
  • Make sure melting temps for yeast DNA regions are nearly equal +/- 1-2 degrees best (so that lengths are nearly equal)
July 26th, 2011

Purpose:

  • Cook all my ligation rxns for 10min at 65 degrees Celsius
  • Digest available ORFs with BsaI in preparation for gel purification
  • Strategy: Take bare minimum (may need to redo)
July 27th, 2011

Purpose:

  • Gel purify ORFs
  • Digest PTZ14u with BsaI to load with other 4 samples

Procedure:

  • Gel lanes: Ladder, A C D E PTZ19u

Results:

  • Gel Pic: Lab:20110727 orf extraction 1.jpg?linkonly
  • A is suspect, may be contaminated with upper band
  • C is inseparable on this gel
  • Mixed D and E, must redo and repeat July 26 digest
  • Run bigger and longer gel next time
July 28th, 2011

Purpose:

  • Gel extractions on long plate (300uL TTE and 3g agarose and 15uL EB)
  • Procudure:
  • Run for 1.5hr at 150V
  • Lanes: Ladder, A C, Ladder, D E, Ladder
  • Make new wide, thin gel (1.5% to run at 100-120V). Tape combs together and add 12.5uL per well.

Results:

  • Blue band at ~300bp, gel was slow
July 29th, 2011

Purpose:

  • Run gel for 2hrs
  • Purify what you can. If time permits, set up a double digest.

Results:

  • Gel Pic: Lab:20110729 orf extraction run 1.jpg?linkonly
  • DNA did not diffuse from the refrigeration. (Don't try to do too much in a day)
  • A and D melting gel at 48 degrees Celsius, closest block available
  • A: 3.2ug/uL
  • D: 9.1ug/uL
  • C: highly suspect of contamination, 10.8ug/uL
August 1st, 2011

Purpose:

  • Transform B1, 2, 3
  • Make 6x XGal plates (1 for 2hrs, one for overnight)

Procedure:

  • 2hr: 50 and 500 uL
  • Overnight: 50 and 500uL (no DNA, just vector only)
August 2nd, 2011

Purpose:

  • Transform B 1, 2, 3
  • Digest promoters with BsaI
  • ligate to appropriate ORFs
August 4th, 2011

Purpose:

  • Digest vector with XbaI and XmaI at 37 degrees Celsius for 0.5hr.

Procedure:

Results:

  • some wells too shallow
August 5th, 2011

Purpose:

  • Ligation and transformation

Results:

  • Did not digest vector first
  • added wrongly-digest vector
August 6th, 2011

Purpose:

  • Prep PTZ19u for ligation
  • Prep ligations to add digest vector

Procedure:

  • 200uL PB, vortex, column, spin for 1min, discard, add 750uL of TE, spin for 1min, discard, spin for 1min @1300rpm, discard, add 25uL EB, spin 1min (into new tube), nanodrop
  • Add 25uL of water, 3uL T4, 3uL ligase. Split to three tubes, each containing 20uL. (Label 1:3, 1:5, 1:10)
  • Add 1, 2, 3 to right tubes, add 1 to vector tubes.
  • Ligate 2hrs overnight, transform 1uL, ligate
August 22nd, 2011

Purpose:

  • Draw up offcut ligation for RFC assembly standard

Procedure:

  • Digest 30uL E180 16-1 (7/2/2011) and run it by two purified ORFs
  • Run 20-well gel (thin comb, B2-20, 200mL 1% agarose with EB). Load 50ug

Results:

  • Purify E, use rest of digest product
August 23rd, 2011

Purpose:

  • End Goal: 58ng scale ligation of VioE to its TDM3p and RPL8a utr

Procedure:

  • Gel purify what's left of digest (took 10uL out of 40uL solution)
  • Run 7x8cm gel (100uL, 1% agarose, and 5uL EB)
  • Digest 10uL of each promoter/utr

Results:

August 24th, 2011

Purpose:

  • Overhang PCR
August 25th, 2011

Purpose:

  • Analytical gel of VioE cassette PCR product

Results:

August 26th, 2011

Purpose:

  • End Goal: Ligate VioB ORF to RPS2p & utr (5ug for each part)
  • Gel purify ORF after BsaI digest
  • Digest p & utr

Results:

August 29th, 2011

Purpose:

  • Digest VioB DNA with BsaI and BsaI/XbaI

Procedure:

  • Run 7x8 1% agarose gel for 35min at 150V

Results:

August 30th, 2011

Purpose:

  • Overhang PCR of VioB expression cassette

Procedure:

  • Recommended extension time is 2min at 72 degree Celsius
  • Run 6-well 50mL 7x8 1% agarose gel at 150V (add 2.5uL EB)
  • Lanes: Ladder, 0.5 1 2, Ladder

Results:

September 1st, 2011

Purpose:

  • End Goal: Design, Digest, and Ligation of all 5 Vio genes
  • Nanodrop all products

Procedure:

  • Ligated according to Aug 23rd protocol. Left at room temp.

Results:

  • Lost VioE, re-PCR and gel.
September 2nd, 2011

Purpose:

  • PCR cleanup (Invitrogen)
  • Design ligation, find PUC19 to digest and do it
  • Get reagents for yeast transformation
  • Grow culture (inoculate 10mL YPD with 2uL cells for tomorrow, measure OD and dilute based on murkiness on Sunday)

Procedure:

  • Run 7x8 50mL 1% agarose gel + 2.5uL EB at 150V for 35min
  • Dilute YPD culture, multiply dilution factors by the absorbance reading

Results:

September 6th, 2011

Purpose:

  • Final Plan: Select Auxotroph specific vector, get sequence
  • Re-PCR expression cassettes and digest internal sites
September 7th, 2011

Purpose:

  • Get PRS416 DNA, digest with EcoRI and HindIII
  • Find smallest possible bar and comb

Procedure:

  • Run 150mL 1% agarose gel with 7.5uL EB at 160V
  • Lanes: 300ug 200ug, Ladder, 100ug 50ug 25ug 10ug 5ug 1ug
  • Lanes: 300 200 100(1) 100(10) 50 25 10 5 1(1) 1(10)
  • Lanes: 10 50 300 200 100

Results

  • Water makes ladder float, not sink
September 8th, 2011

Purpose:

  • PCR cleanup products (amplify them)
  • Gel purify PRS416
  • PCR Purify again
  • Gel purify

Procedure:

  • Run 7x8cm gel(50mL, 1% agarose, 2.5uL EB)
  • Lanes: Ladder, A B C D E

Results:

September 9th, 2011

Purpose:

  • Transform ligation misses and no DNA or vector control
  • Redo PCR for VioE

Procedure:

  • Add 5uL positive and negative ligation and 1uL PRS416
  • 2min on ice
  • Heat shock for 45s
  • Ice for 2min
  • Added 450mL SOC to each
  • 1hr on shaking incubator
  • 1 plate (50uL), next plate (centrifuge 7000rpm for 25s)
  • Take 350mL supernatent out, plate rest after resuspension with pipet

Results:

  • Can't tell which tube was PRS416, and no DNA.
September 10th, 2011

Purpose:

  • Miniprep colonies and digest them

Procedure:

  • Run 7x8 50mL 1% agarose gel with 2.5uL EB
  • Lanes: 5uL Ladder, 10uL each of E(new) and E(old)
  • Redid VioE PCR from ligation mix
  • PCR cleanup with Qiagen
  • Gel purify of undigested PCR clean product
  • Run 12x14 150mL 1% agarose gel with 7.5 EB
  • Lanes: A, Ladder, B X, Ladder, C X D, Ladder, E X X

Results:

September 12th, 2011

Purpose:

  • Colony PCR design
September 13th, 2011

Purpose:

  • Colony PCR

Results:

September 15th, 2011

Purpose:

  • Religate in case yeast transformation didn't work
  • Colony PCR
September 16th, 2011

Purpose:

  • Colony PCR gel (each 96-well plate section of 3 rows occupies one gel row)
  • Redigest PRS416 and test plasmid with EcoRI and HindIII

Procedure:

  • Run 7x8cm 50mL 1% agarose with 2.5uL EB gel
  • Lanes: PRS X Ladder, PAR...6wells

Results:

Violacein Biosynthesis in Yeast

Retrieved from "http://2011.igem.org/Team:Johns_Hopkins/Notebook/Vio"