Team:BGU ISRAEL/Notebook
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When - 23/06/16
Who's In the lab today: Ben and Dar
glycerol stock protocol:
-
preparing glycerol:
- add 10 ml LB to 10 ml glycerol
-
preparing the stock:
- take 500 ul of starter (with required plasmid transfected)
- add 500 ul of the glycerol (from stck)
- freeze in -80 C
When - 15/06/16
Who's In the lab today: Ben and Dar
We isolated the plasmids from each cell culture using Geneaid
Again we incubated them with XhoI and XbaI (same protocol as on 14/06)
We ran the samples on a 1% agarose gel with EtBr but using a new loading buffer.
In lanes 6,7,8 we can see good results.
Lane 6 shows the plasmid circular and uncut.
Lane 7 shows the plasmid cut in one location using XbaI.
Lane 8 shows the plasmid circular and uncut (as it does not have a XhoI restriction site).
starters growth for activity testing of LCC:
LB 50 ml+ CP 50 ul.
each tube will get 5 ml.
In addition, LB 5ml without antibiotic for BL21 growth without insertion.
For each tube. we added colony with another varient+2 control tube.
the colony that we are testing:
pACYC LCC WT C6
pACYC LCC C.O C4
pACYC LCC F4 C2
pACYC LCC F7 C3
pACYC LCC R4 C7
pACYC LCC R7 C2
pACYC no insert
BL21 (without antibiotic)
Turbidity check and induction:
For LB 7 ml + CP 7ul we added 70 ul for each starter. ( 37C 200 rpm)
PET degradation test:
we cheked if there is any change in PET wight after one day:
When - 14/06/16
Who's In the lab today: Ben and Dar
We isolated the plasmids from each cell culture using Geneaid Presto mini plasmid kit.
We Incubated each of the plasmids with XhoI and XbaI restriction enzymes (2 hours incubation in 37 degrees and 20 minutes in 65 degrees).
We ran the results in a 1% agarose gel with EtBr.
Both plasmids show on the gel uncut (lanes 2-3). We have no ability to determine their size (as they are circular).
We put new starters for another preparation of plasmid DNA.
When - 13/06/16
Who's In the lab today: Ben and Dar
We incubated starters for the pSEVA224 and pSEVA414 in 30 degrees.
When - 10/06/16
Who's In the lab today: Eyal
preparation of TRIS-HCL:
- for prvpB degredation---> C1V1=C2V2→ 1M*V1= 25mM*9.9ml→ V1=247.5 ul, DDW=9.6525ml
- for PET degredation---> C1V1=C2V2→ 1M*V1= 500mM*2ml→ V1=1ml, DDW=1ml
preparation of pNP-B:
- pNPB - 35ul -----------> 1 ml of pNPB ---------> 100 mM into
- acetonitrite - 965 ul --------> in 200 mM conc. ----->9.9 TRIS 25 nM
we left 8 tubes with LCC variants for incubation at 10:30 AM for the weekend (50 C)
When - 06/06/16
Who's In the lab today: Eyal
we designed an expriment to test differnet carbon surce from our metabolic pathway for putida.
We used 96DW and we orgenized it as seen in the picture:
this experiment will last for one week we will check the change in the turbidity with plate-reader.
When - 31/05/16
Who's In the lab today: Eyal
we cut De-lorenzo plasmids (414+224), we run thus plasmids on agar gel for analazing if thus plasmids were cut.
When - 28/05/16
Who's In the lab today: Eyal
starters for Putida KT2440.
5 ml LB+5 ul amp, 100ng/ul, 30C
transformetion for pACYC plasmid without insertion(negative control for coplement cells) and with insertion LCC WT C6, LCC CO C4, LCC F4C2, LCCF7C3, LCC R4C7, LCC R7C2 to BL21 bacteria for protein exprection.
- 8 tubes with compatent BL21 bacteria, 80C,10 min.
- 1 ul from each plasmid for each tube.
- mixed with tip.
- keep in ice for 20 min.
- keep in ice for 3 min more.
- 500 ul SOC without antbiotic.
- 27C 1h
- centrifugation 5000 rpm 2min
- take off 500ul from the liquid.
- mix the residue with the rest liquid.
- sowing in LB+CMP
When - 24/05/16
Who's In the lab today: Eyal
seq of LCC variants 3 ul primer in each reaction 300 ng DNA.
(each with Rw\Fw primer).
When - 19/05/16
Who's In the lab today: Roee and Neomi
We made plates with : LB+TET, LB+Strep. we took the starters with De-Lorenzo bacteria to swo on thus plates.
After all the starters and glycerol stocks were found contaminated a new plate of rhodococcus ruber was recieved from alex sivans lab. a new SM medium was made and we have set the tools inorder to grow new starters on sunday may the 22nd.
When - 13/05/16
Who's In the lab today: Eyal
Constructing a growth-curve for the Putida on Cathecol. The experiment was contaminated. we will have to repete it.
When - 11/05/16
Who's In the lab today: Eyal
pSEVA starters from 10.5, and sowing on LB+KM 2 ml starters 300 rpm, 2 min, RT, using sup and sowing the output.
When - 03/05/16
Who's In the lab today: Eyal, Roee and Dor
one colony from each plate was sent fot seq(because of the bw concentration, 15 ul from each stock was sent)
2 starters of rhodococcus ruber were made from two different glycerol stocks to check for contamination. each sample was plated on a nutrient agar plate that was divided in to two parts one for each glycerol stock. the starters were put in ramons lab in the incubator shaker 37 degrees and the plate was put in our incubator at 37 degrees as well.
we prepered glycerol stocks of BL21.
When - 25/04/16
Who's In the lab today: Eyal
| reaction 1 | reaction 2 | reaction 3 | reaction 4 | reaction 5 | reaction 6 | reaction 7 | |
|---|---|---|---|---|---|---|---|
| LCC W.T | LCC C.O | LCC F4 | LCC R4 | LCC F7 | LCC R7 | control | |
| pACYC | 1.8 | 1.8 | 1.8 | 1.8 | 1.8 | 1.8 | 1.8 |
| Insert | 0.9 | 1.3 | 0.6 | 0.8 | 0.9 | 0.8 | - |
| Buffer | 2 | 2 | 2 | 2 | 2 | 2 | 1.4 |
| DDW | 14.3 | 13.9 | 14.6 | 14.4 | 14.3 | 14.4 | 15.2 |
| Ligase | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
incubeted at 16C
M9 salts add to 800 ml H2O:
- 31.64 gr Na2HPO4*2H20
- 15 gr Kh2PO4
- 2.5 gr NaCl
- 5.0 gr NH4Cl
stirr until dissolved
adjust to 100 ml with distilled H2O
make M9:
- 700 ml DDW
- 200ml M9 salts
- 2 ml 1M MgSO4
- 100ul 1M CaCl2
- adjust to 980 ml with DDW
When - 19/04/16
Who's In the lab today: Efrat
Cyclic Voltametry was preformed in oreder to mesure Cathecol’s redox porential conditions:
- 2% wt Catechol solution in M9. Potential range:
- 0-0.5 V.E step: 0.005 V
- scan rate: 0.01, 0.005, 0.001 V. Room temperature, pH 7
| 0.005 V | 0.01 V | 0.001 V | |
|---|---|---|---|
| E for I max | 0.324797 | 0.334791 | 0.41574 |
| E for I min | 0.119925 | 0.099937 | 0.131918 |
| Delta E | 0.204872 | 0.234854 | 0.283822 |
| E 0 | 0.222361 | 0.217364 | 0.273829 |
When - 18/04/16
Who's In the lab today: Ben
I loaded the PCR products from yesterday onto an agarose gel (1.5%).
The results:
- Lane 1: 1kb plus ladder
- Lane 2: pcaG (~660bp)
- Lane 3: pcaH (~760bp)
- Lane 4: pcaC (~450bp)
- Lane 5: pcaD (~840bp)
When - 17/04/16
Who's In the lab today: Ben
I ran a colony-PCR on P. putida with primers for the 4 protocatechuate degredation genes (pcaG/H, pcaC/D)
The reaction mix was:
- 25μL of ReadyMix Taq PCR reaction mix
- 22μL of UPW
- 1.5μL of each primer
- A swab from a P. putida colony.
(total reaction volume 50μL)
Cycle parameters were according to Sigma-Aldrich protocol.
ligation of LCC variants into pACYC vector.
Using a ligation calculator in 3:1 ration: we will use about 36 ng of insert for each ligation reaction:
| reaction 1 | reaction 2 | reaction 3 | reaction 4 | reaction 5 | reaction 6 | |
|---|---|---|---|---|---|---|
| LCC W,T | LCC C.O | LCC F4 | LCC R4 | LCC F7 | LCC R7 | |
| pACYC | 1.4 | 1.4 | 1.4 | 1.4 | 1.4 | 1.4 |
| Insert | 0.9 | 1.3 | 0.6 | 0.8 | 0.9 | 0.8 |
| Buffer | 2 | 2 | 2 | 2 | 2 | 2 |
| DDW | 14.7 | 14.3 | 15 | 14.8 | 14.7 | 14.8 |
| Ligase | 1 | 1 | 1 | 1 | 1 | 1 |
+control: pACYC 1.4, Buffer 2, DDW 1, Ligase 1
-Incubated overnight at 16C
prepered LB agar plates whith CAM resistance.
When - 13/04/16
Who's In the lab today: Inbar B, Inbar S and Eyal
we took Rodococus rubber from glycerol stock and plated on te LB plate at the biological hood.
When - 12/04/16
Who's In the lab today: Eyal, Inbar B and Inbar S
we have made 2 plates containing only LB.
we have made 8 plates containing LB+CRB.
colonies were present.
two- 5 ml starters from CAM plate (pACYC) for midiprep and miniprep.
starter for midiprep 200 ml
midiprep.
When - 11/04/16
Who's In the lab today: Inbar B, Inbar S and Eyal
we took new pACYC from eyal arbely lab, we transformed E. coli it to mg1655 and seed it on CAM plate.
When - 08/04/16
Who's In the lab today: Tomer
we have made 3 medium with glucose, PET, PolyEthylene and palced them in 37C shaker.
When - 06/04/16
Who's In the lab today: Tomer and Ben
restriction of pACYC and E1B GFP
-
- E1B GFp 1 ul
- 3.1 buffer 5 ul
- XhoI 1ul
- DDW 43 ul
- pACYC 5 ul
- 3.1 5 ul
- XhaI 1 ul
- DDW 39 u
- Added 1ul BglII incubeted at 37 C
-
Glycerol stock made for putida:
- 500 ul from starters
- 500 ul glycerol 30 % +LB
making a startersfor Rodococus rubber:
We took 50 ml of SM+Glucose and added to it some of the glycerol stock.
When - 05/04/16
Who's In the lab today: Dar, Tomer and Ben
we prepared new LB medium (1L), gathered and prepared glassware for autoclave.
we set up startes for the Putida - for growth experiments and for preparing new glycerol stocks.
We prepared a 20% (w) Catechol solution using 10gr of Catechol (Pyrocatechol from Sigma-Aldrich) and 50ml of DDW.
We prepared M9 Catechol medium using:
- 10ml M9 Salts
- 5μL CaCl2 (1M)
- 100μL MgSO4
- 39ml DDW
- 165μL Catechol 20%
When - 31/03/16
Who's In the lab today: Dar
checking whether the Putida from the experiment last week (Growth curves for Putida and E.Coli on EG) are still alive (and that the OD we’ve measured isn’t the result of dead bacteria).
at both times samples were taken from the liquid solution in the tub and put on plates (LB+amp). at both times growth on the plates was observed - the bacteria were still alive.
When - 28/03/16
Who's In the lab today: Inbar S and Eyal
Try #3 of the pACYC restriction
This time - 1 hour with each enzyme and run on agarose gel 2ul after each cut.
- pACYC 2000ng 30ul(66ng/ul)
- DDW 58ul
- 3.1 Buffer 10ul
- XhoI 1ul
- 1 hour 37 deg
- 20 min 65 deg
- 1 ul BalII
- 1hour -> run on agarose gel 2ul.
When - 28/03/16
Who's In the lab today: Inbar S and Eyal
Another restriction reaction for the pACYC plasmid.
We used the pACYC2 product from 25/03(68ng/ul) - Restriction requires 2000ng of plasmid DNA so we used a volume 29.4ul.
Reaction protocol:
- DNA 29.4ul
- 3.1 Buffer (NEB) 10ul
- BalII 1ul
- XhoI 1ul
- DDW 58.8ul
No Bands again.
When - 27/03/16
Who's In the lab today: Dar
Setting up the growth-curve experiment for both the Putida and E.Coli (MG1655) on Ethylene Glycol.
This time the experiment will take a week - 2-3 measurements per day.
When - 25/03/16
Who's In the lab today: Inbar
Mini-prep for pACYC.
| Concentration (ng/uL) | 260/280nm | |
|---|---|---|
| pACYC1 | 66 | 1.81 |
| pACYC2 | 68 | 1.78 |
When - 24/03/16
Who's In the lab today: Tomer and Inbar Bariah
Removing the putida starter from the incubator to the fridge.
DNA extraction from reaction mix- LC-cutinase variants.
total volume 30ul
| LC-cutinase variant | concentration(ng/ul) | 260\280 |
|---|---|---|
| lc-cutinase - WT | 43 | 1.63 |
| lc-cutinase - WT CO | 28 | 1.52 |
| FreeRun4 | 61 | 1.71 |
| FreeRun7 | 47 | 1.66 |
| ResRun4 | 41 | 1.69 |
| ResRun7 | 46 | 1.64 |
WT, WTCO, F4, F7, R4, R7, 1KbPlus led
In addition, starters for pACYC were prepared:
10ml LB+10uL CAM for 2 starters.
When - 23/03/16
Who's In the lab today: Inbar Segal, Dar, Ben, Inbar B, Roee, Dor, Tomer and Eyal
Produced the pACYC plasmid from the starter and cleaned it using mini prep kit.
Concentration: 52ng/ul 260\280: 1.83
another try at constructing a growth-curve for the Putida and E.coli on Ethylene glycol and Glucose.
Setting up new starters for the Putida and E.coli (MG1655)
When - 22/03/16
Who's In the lab today: Eyal and Inbar Segal
Cutting LC-cutinase and pACYC vector with restriction enzymes, no bands were visible on electrophoresis gel.
When - 18/03/16
PCR extraction of LC-cutinase variants
total volume 30ul
| LC-cutinase variant | concentration(ng/ul) | 260\280 |
|---|---|---|
| lc-cutinase - WT CO | 134 | 1.81 |
| FreeRun4 | 143 | 1.79 |
| FreeRun7 | 133 | 1.80 |
| ResRun4 | 110 | 1.78 |
| ResRun7 | 138 | 1.81 |
When - 17/03/16
Who's In the lab today: Inbar Bariah
PCR to amplify LC-cutinase variants: WT CO, FreeRun4, FreeRun7, ResRun4, ResRun7.
WTCO, WTCOX,F4,F4X,F7,F7X,R4,R4X,R7,R7X,1KbPlus led
When - 15/03/16
Who's In the lab today: Ben, Dar, Roee and Tomer
We tried constructing a growth curve for E. coli and P. putida on Glucose and Ethylene Glycol.
The Experiment failed (the O.D was declining instead of increasing), probably because the starters we used were kept in the refrigerator for more than 4 days (the bacteria were probably dead).
When - 08/03/16
Who's In the lab today: Eyal and Inbar Segal
we did a transformation to PACYC, using 50microliter competent bacteria.
100 microliters were used for plating.
an activity test was made of DPNI - we did a transformation in order to check that the plasmid indeed dissolved (nothing is supposed to grow).
concentrations of the genes we received from Weizmann institute:
- Lc-cutinase - WT - 26.55 ng/ul
- FreeRun4 - 19.15 ng/ul
- FreeRun7 - 15.575 ng/ul
- ResRun4 - 20.175 ng/ul
- ResRun7 - 25.575 ng/ul
When - 25/02/16
Who's In the lab today: Ben
went to the supply room to bring in supplies:- one measuring cup 2L made of glass, and one 1L measuring cup made of plastic.
- 20ml syringes and 10ml syringes - 10 from each volume. and a few more 2.5 ml because they didn't have 5ml syringes.
- around 30 minisart filters.
- latex gloves Medium size x5.
- A bundle of glass pipettes 10ml (they didn't have 20ml ones) we need to order especially.
- big tank for water (needs a wash and then we can use it for ddw or upw).
When - 24/02/16
Who's In the lab today: Neomi, Tomer and Dor
a glycerol stock of rhodoccocus ruber was prepared from the starter made yesterday. I didn't know if the glycerol in our fridge was autoclaved so I borrowed from Ramon's lab, the stock is at (-80) degrees Celsius at Ramon's shelf.
Removed the putida from the incubator after growing on ethylene glycol and glucose and checked the OD (600nm)
Results:
| Tube | OD (600nm) |
|---|---|
| Glucose 20% | 0.686 |
| Glucose 15% + Ethylene Glycol 5% | 0.420 |
| Glucose 10% + EG 10% | 0.859 |
| Glucose 5% + EG 15% | 0.112 |
| Ethylene Glycol 20% | 0.465 |
because the measurements were inconsistent I made several measurements. especially tubes 1 and 5:
| Tube | OD (600nm) |
|---|---|
| Glucose 20% | first re-measurement 0.459 second re-measurement 0.611 |
| Glucose 15% + Ethylene Glycol 5% | first re-measurement 0.019 second re-measurement 0.032 |
When - 23/02/16
Who's In the lab today: Ben and Roee
- a starter of Rhodococcus ruber was made. it included 50ml SM(medium) + glucose + microelements. the work was done in a biological hood afterwards it was placed in a shaker at 37 degrees Celsius overnight.
-
taking the putida out of the shaker after growing it on glucose and ethylene glycol and checking OD (600nm).
Results:
| Tube | OD (600nm) |
|---|---|
| Glucose 20% | 0.560 |
| Glucose 15% + Ethylene Glycol 5% | 0.671 |
| Glucose 10% + EG 10% | 0.465 |
| Glucose 5% + EG 15% | 0 |
| Ethylene Glycol 20% | 0.09 |
When - 21/02/16
Who's In the lab today: Roee, Dar, Dor and Neomi
how to make competent bacteria?- all the process need to occur on ice, in a centrifuge set to 4degree Celsius, and the glycerol need to be cold.
- first of all, we grow the bacteria over night with antibiotics -> in 50 ml falcon tube.
- centrifuge - maximum speed for 15 min and remove the supernatant.
- we fill the falcon tube again with glycerol 10%. centrifuge once again for 15 min at max speed and again remove the supernatant.
- repeat step 2.
- we combine both tubes (if we have more than one, if not we wash it again with glycerol as we did in 2+3) after we fluidize the bacteria in glycerol we complete the volume with 10% glycerol, we centrifuge and remove the supernatant.
- fluidize the sediment with 2 ml glycerol and divide into tubes 50 microliter in each one and freeze with liquid nitrogen.
a medium for growing Rhodococcus Ruber was made in the solution are missing microelements that we are supposed to receive from Valentina and there is no carbon source. the solution is in the fridge door with a sticker “rhodococus ruber solution”.
When - 22/02/16
Who's In the lab today: Roee, Dar, Dor, Tomer, Inbar Segal and Eyal
competent bacteria were made from the putida KT2440 strain. the bacteria were divided into 25 Eppendorf's with 50microliter each (the volume needed for each transformation) the Eppendorf's are in the freezer (-80 degrees) of Ramons lab in a red box the with the inscription “Ashalim”.
starting the experiment of growing the Pseudomonas putida on ethylene glycol:- we made the minimal medium where each one has different rates of carbon sources.
- we inserted to each medium one colony of Pseudomonas Putida.
- we made a blank of 1ml to measure OD.
- we put the bacteria in a Shaker set to 37 degrees Celsius in Naama's lab.
We did a PCR reaction for the LC-Cutinase + leader Sequence Gene. in order to take it from the iGEM plasmid and insert it into a PACYC vector. we ran the PCR products on an agarose gel using electrophoresis and took a picture. we got one big band in the size we wanted 1KBP~ and a second band, weaker one in the size of the entire plasmid.
When - 15/02/16
Who's In the lab today: Inbar Bariah
main action - growing two strains of Pseudomonas putida on SOC (EM383, KT2440):inserting a Q-tip that touched the glycerol stock of the relevant culture into 3ml of SOC with ampicillin (needs to be near fire) and growing overnight. -results- the bacteria grew and the medium became very murky. the bacteria were afterwards grown on petri dishes with LB + amp from every strain we inserted 20 microliters and we also made plates where we isolated via striking.
colonies from every strain (KT2440, EM383) were moved into a liquid LB medium for incubation overnight in 37 degrees Celsius.
When - 14/02/16
Who's In the lab today: Inbar Bariah, Neomi and Tomer
main action - making M9 medium for growing Pseudomonas PutidaInstead of glucose as a carbon source we planned an experiment where the ratios between glucose and ethylene glycol vary in order to check if the bacteria can use ethylene glycol as a carbon source. if so, we won't need to insert the two plasmids we took from E. coli.
planning the experiment - we divide the medium into 5 different test tubes where the carbon source will be different in each one:- 100% glucose.
- 75% glucose, 25% ethylene glycol.
- 50% glucose, 50% ethylene glycol.
- 75% ethylene glycol, 25% glucose.
- 100% ethylene glycol.
- with the assistance of Idit we made MgSo4 and a Salt sterile solutions using autoclave.
- we used Sterile CaCl that already gone through autoclave and also DDW that we already had in the lab.
- we made 20% glucose and filtered it.
- we filtered ethylene glycol and made a 20% ethylene glycol solution.
- weighing 1g ampicillin.
- adding 10ml DDW.
- filtering with syringe 0.24 wide.
- dividing it into 20 Eppendorf's (500microliter each).
When - 02/02/16
Who's In the lab today: Roee, Inbar Bariah and Tomer
main action - re-sending the two plasmids that got low percentages to sequencing again.after checking once again the sequences in blast of the two plasmids that got low percentage and after consulting with Dr.Birnbaum and Naama we understood that the way we looked at the percentage wasn't correct and that the sequencing was actually correct and we had the sequence we wanted on the plasmid. (before we knew about the sequencing being correct we made Chloramphenicol in working dosage in order to grow the bacteria that carried the plasmid on the medium we wanted).
instructions for sending DNA to sequencing:- Plasmid Dosage need to be between 75-100 ng/ul.
- volume needed: ten microliters per plasmid.
- Primers - 2 microliters per sequenced plasmid (minimum volume 5 ul).
When - 18/01/16
Who's In the lab today: Inbar Segal
Preparation of competent bacteria: E. coli MG1655- Add all of the starter to 500 ml of LB
- Use 1 ml of LB as blank, measure OD at time zero at wavelength of 600 nm. (time zero was 0.064 nm)
- Measure OD every hour until the bacteria gets to the logarithmic phase (about 3 hours).
- Incubar, Shaker, Spectofotometer were used in Ofer yifrach lab (3 floor).
- At 11:20 OD was 0.54 nm, we took it out of the shaker and put it in ice.
- We checked if the bacteria can grow on agar with kan and amp - we did not see any colony.
When - 17/01/17
Who's In the lab today: Dor, Inbar Barih and Neomi
How to make a solution for competent bacteria:
When - 14/01/16
Who's In the lab today: Dor, Roee, Tomer and Naama
How to check the results of sequencing:- Open the file with the graphs displaying the output.
- Go to edit->copy seq->FASTA format.
- Go to Blast and paste what we copied in the first window, if we copied first the sequence of the foreword primer after we will do for the reverse primer and vice-versa.
- Open the file with the graphs displaying the output, but this time for the reverse primer if we opened its first for the foreword and vice-versa.
- Go to edit->copy seq->FASTA format.
- Go to Blast press enter, and paste this part in the same window one row below.
- Take the reference and put in a different box/one row below.
- Press Blast
- In the top of the page in Blast you can check if R or F fits the reference.
- It's better to check if R and F match (we expect it to be similar not the same).
- Notice the values of query-how similar are the samples, ident-percentage of identical bases.
- Look where most of the different bases are located (hopefully in the end or the beginning).
- Small letters instead of big ones (atg and not ATG) marks that this sequence repeats itself.
- If you to write comments, write according to the locations of the reference.
- Look at the map of the vector that was sent (for the Putida) try to see which restriction enzymes are relevant.
- Go to the website-nebcutter, check for each of the fragments which restriction enzymes are relevant (each fragment separately, according to the reference).
- press custom digest for the list of enzymes, check that this enzyme don't cut inside of the fragments.
- choose restriction enzymes.
- Plan primers with tails that will match the enzymes.
- pcr and ligation.
- transformation.
When - 31/12/15
Who's In the lab today: Liran and Tomer
Measuring DNA concentration of the plasmids (the numbers match the ones from above):| Plasmid | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| concentration (Nano gram/ ul) | 222.96 | 188.87 | 159.67 | 125.30 | 98.86 | 293.56 | 153.54 | 189.91 | 155.54 | 157.45 | 166.29 |
When - 30/12/15
Who's In the lab today: Ben, Liran, Dar, Tomer and Dor
Pcr for two genes (aldA, flco) of the E.coli strain MG1655:- Prepration of a DNA gel
| Well | 1 | 3 | 4 | 6 | 7 |
|---|---|---|---|---|---|
| Sample | ladder | flco | flco control (no template) | aldA control (no template) | aldA |
| Number | Plasmid |
|---|---|
| 1 | tph A1 |
| 2 | tctA A1 |
| 3 | tph A3 |
| 4 | LC cutinase |
| 5 | LC cut + lead seq + his tag |
| 6 | tph A2 |
| Number | Plasmid |
|---|---|
| 7 | tphB |
| 8 | tctA A2 |
| 9 | rctB B1 |
| 10 | tph C |
| 11 | LC cut + lead seq |
When - 29/12/15
Who's In the lab today: Inbar Barih, Inbar Segal, Eyal, Liran and Ben
Making starts for bacteria after Transformation:- Add 5 ml of LB to a 50ml falcon.
- Add 5 ul of the matching antibiotic (the ratio is 1:1000).
- With a toothpick stab one colony spread it on another Agar plate (in case the starter wont work we will be able to use that colony again) and then throw it inside of the 50 ml flacon.
