Team:Toronto/Notebook-w18-fri

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Friday, September 16

Sunday, 9/18
Members Present: Cathy Cao , Alexander Sullivan, Hamed Tinafar
LAB:
Afternoon:
Checked on the 96-flat-well plates after 48 hours based off of the experiment taken place on Wednesday, September 14 (absorbance results can be see on this file: https://drive.google.com/file/d/0B6Z4m6vl-WRuZm1jdHhHM1d4em8/view?usp=sharing )
iGEM_2016_-_Control_Sept_14.xlsx
IMG_20160916_185228.jpg
thumbnail
(R=Row, C=Colume): RAC1: mRFP1 (faint) - There is no distinct colour present in here as there is no CPRG present (or LB for it to grow plentifully) RAC2: mCherry (faint) - There is no distinct colour present in here as there is no CPRG present (or LB for it to grow plentifully) RAC3: LacZ1+1mM CPRG - The LacZ that is being expressed is able to cleave the yellow CPRG into a purple subtrate (as seen here). NOTE: The clear center could be due to it drying up as this is 48 hours after initial test RAC4: LacZ2+1mM CPRG - The LacZ that is being expressed is able to cleave the yellow CPRG into a purple subtrate (as seen here) RAC5: LacZ2+1mM CPRG - The LacZ that is being expressed is able to cleave the yellow CPRG into a purple subtrate (as seen here). NOTE: The clear center could be due to it drying up as this is 48 hours after initial test RAC6: pgolB_LacZ+1mM CPRG - The LacZ that is being expressed is able to cleave the yellow CPRG into a purple subtrate (as seen here) RBC1: mRFP1 (faint) - There is no distinct colour present in here as there is no CPRG present (or LB for it to grow plentifully) RBC2: mCherry (faint) - There is no distinct colour present in here as there is no CPRG present (or LB for it to grow plentifully) RBC3: LacZ1+5mM CPRG - The LacZ that is being expressed is able to cleave the yellow CPRG into a purple subtrate (as seen here). Darker than the row above (RA) due to it having more CPRG in the well. NOTE: The clear center could be due to it drying up as this is 48 hours after initial test RBC4: LacZ2+5mM CPRG - The LacZ that is being expressed is able to cleave the yellow CPRG into a purple subtrate (as seen here). Darker than the row above (RA) due to it having more CPRG in the well. NOTE The white dots on top of the well is a thumb smudge. RBC5: LacZ2+5mM CPRG - The LacZ that is being expressed is able to cleave the yellow CPRG into a purple subtrate (as seen here). Darker than the row above (RA) due to it having more CPRG in the well. NOTE The white dots on top of the well is a thumb smudge. RBC6: pgolB_LacZ+5mM CPRG - The LacZ that is being expressed is able to cleave the yellow CPRG into a purple subtrate (as seen here). Darker than the row above (RA) due to it having more CPRG in the well. NOTE The white dots on top of the well is a thumb smudge. RCC1: Lb - No colour visible here as only a small amount of Lb was added. Nothing should be visible here as it can be an indication for base contamination RCC3: LacZ1 - This well is not distincty yellow or purple as no CPRG was added. The yellow-ness around the bottom of the well is due to the bacteria. RCC4: LacZ2 - This well is not distincty yellow or purple as no CPRG was added. The yellow-ness around the bottom of the well is due to the bacteria. RCC5: LacZ3 - This well is not distincty yellow or purple as no CPRG was added. The yellow-ness around the bottom of the well is due to the bacteria. RCC6: pgolB_LacZ - This well is not distincty yellow or purple as no CPRG was added. The yellow-ness around the bottom of the well is due to the bacteria. RHC3: DH10B+1mM CPRG - A CPRG negative control where only E. coli K12 DH10β was added to a solution of 1mM CPRG. This was used to keep the sample as yellow as possible though now it is a bit faint as it has begun to try up. RHC5: BL21+1mM CPRG - A CPRG positive where BL21 (is not LacZ deficient) was added to 1mM of CPRG. This was used to keep the sample as purple as possible though now it is a bit faint as it has begun to try up.
A
B
C
D
E
F
G
1
123456
2
AmRFP1 (faint)mCherry(faint)LacZ1+1mM CPRGLacZ2+1mM CPRGLacZ2+1mM CPRGpgolB_LacZ+1mM CPRG
3
BmRFP2(faint)mCherry(faint)LacZ1 +5mM CPRGLacZ2+5mM CPRGLacZ2+5mM CPRGpgolB_LacZ+5mM CPRG
4
CLBLacZ1LacZ2LacZ3pgolB_LacZ
5
HDH10B+1mM CPRGBL21+1mM CPRG
Table1
Administrative:
Meet with OG regarding:
Genomics in the Park
Attendee: Ben (P&P), Alexander Sullivan, Jordan (OG)
Ben (University of Toronto) and Ayan (Waterloo University) are confimed to go
Jordan from OG will be designing the poster
We have to design the broucher
Synthetic Biology Network Platform (P&P project)
Attendee: Alexander Sullivan, Shivali (P&P), Fahim (Dry lab), Sana (OG), three people from ORION
We got the server
1 year on server, renew in one year if we wish to continue
OG wants long-term plan
TO DO:
For the next day:
Culture cells and miniprep
Miniprep for sequencing and Concordia iGEM collaboration
Start AuCl assaying if we have new plates and the AuCl are in
LAB MANAGERS: (For Zarifah Omar Ali, Bohdan Lukach)
Dishwashing
Pick up IDT orders that have arrived at Phil's (WB basement)
Autoclaving pipette tips and anything else needed