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Team:SouthBend-Mishawaka-HS/Notebook
From 2011.igem.org
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==Tranformation== | ==Tranformation== | ||
| - | Decided to Transform E.col: with the F2620 part as back up. We follow this procedure. | + | Decided to Transform E.col: with the F2620 part as back up. We follow this procedure.<br> |
| - | (1)105 E.col: calls were added to 100ul BioRad Transformation Solution. | + | (1)105 E.col: calls were added to 100ul BioRad Transformation Solution.<br> |
| - | (2)1ul of F2620 DNA from the Registery was added to the cells which were incubated 30min on ice. | + | (2)1ul of F2620 DNA from the Registery was added to the cells which were incubated 30min on ice.<br> |
| - | (3)Cells were heat shocked by swirling in water at 42 degree water bath for 2min. than return to ice for 30min. | + | (3)Cells were heat shocked by swirling in water at 42 degree water bath for 2min. than return to ice for 30min.<br> |
| - | (4)1ml 50B butter was added to the cells and they were incubated for 2 hrs. at room temp. | + | (4)1ml 50B butter was added to the cells and they were incubated for 2 hrs. at room temp.<br> |
| - | (5)100ul of the transformed cells were plated on a fresh LB/AMP plate. | + | (5)100ul of the transformed cells were plated on a fresh LB/AMP plate.<br> |
Revision as of 15:59, 1 June 2011
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May
May19
Today we did our first transformation via heat shock.
(1)Poured 12 LB AMP plates:(2mg of Ampicillin to 250ml of Agar)
(2)Obtained a vial of 2 microliters of TOP-10 electrocompetant E. coli cells (44-0003/793762)
(3)Added 50 microliters of pure water from the Gemini machine
(4)Added 10 ul of water to well 6E of plate 2, which contained part F2620.
(5)Added 2 ul of the diluted DNA in 50 ul of transformation solution (50mm CaCl2, pH 6.1 BIO-RAD Transformation Solution control # 31000008916 recieved 1-17-11 GT).
(6)Incubate on ice for 5 minutes
(7)Heat shocked at 40 degrees Celcius for 50 seconds
(8)Incubated at 4 degrees Celcius for 5 minutes
(9)Added 1mL of LB (5-17-11 DG)
(10)Plated 100 microliters and 25 microliters of transformed cells on LB-AMP (5-19-11 "crew")
May 18
We found no growth on the plates. We are going to re-transform them next week, this time using electricity instead of heat-shock.
May 24
Today we are re-transforming bacteria with the F2620, this time with electricity.
(1)Obtained 40 microliters of electrocompetent TOP-10 E. coli cells.
(2)Added 2 microliters of F2620.
(3)Zapped with 1.8kV for 5.8ms.
(4)Recovered with 900 microliters of SOB to recover cells
(5)Incubated for 1hr. Then plated the newly transformed cells.
We expect 10 to 50 colonies
May 25
Results: Lawn of bacteria!
Conclusion: No selection because AMP on plate is no good? Or maybe we had a fabulous transformation!
We replaced 100mL on LB AMP agar (5/25/2011)
We, again, expect 10 to 50 colonies
May 26
Results: No growth! This may be a result of no transformation or bad AMP on 4/21/11 plate... transformants may be present, however.
Qtip swabbed up lawn and resuspended in AMP LB broth
Time....................A600
0 hr..................... 0.210
1 hr..................... 0.123
2.5 hr.................. 0.110
Results: absorbance declining means cells are dying... they are not transformed.
Will leave in incubator overnight to see is transformants grow out!
Next step: Try again!
So, we began another new transformation. Again, we are using heat-shock to induce the cells to take up the DNA.
(1)Obtained a vial with 40 microliters of competent cells.
(2)Added 5 microliters of transformation solution (BIO RAD, Catalog 166-0409, tec'd 1/17/11 PT)
(3)Left in ice bath for 5 minutes.
(4)Shocked for 50 seconds in 44.7 degrees Celcius water.
(5)Placed back in ice for another 5 minutes.
(6)Added 1 mL SOB media at room temperature.
(7)Plated on LB AMP plates (100 microliters of cells).
We expect 10 to 50 colonies (yet again... hopefully)
May 31
We FINALLY got growth! Last friday, Professor Twaddle discovered our wonderfully transformed (we hope) cells. He took our best colony and placed it in growing broth. Today, we purified and isolated the DNA in order to test the transformation. We will run electrophoresis on our purified DNA next time we meet: this Tursday.
(1)We obtained 10 mL of broth containing our transformed F2620 cells. We centrifuged 2 mL four times until we had a total of 8mL worth of cells in our pellet.
(2)We added 250 microliters of resuspention solution to the pellet and vortexed.
(3)We then added 250 microliters of lysis solution and inverted. Then, we added 350 microliters of neutralization solution and inverted again.
(4)To isolate our DNA from the solution, we centrifuged for 5 minutes.
(5)Then, we transferred the lysate supernatant to our mini spin/vac column and centrifuged that for 1 minute.
(6)After decanting the flow-through, we added 750 microliters of wash solution. Then, we centrifuged again and decanted the flow-through.
(7)We centrifuged once more for 1 minute to get rid of any residual wash solution.
(8)Finally, we eluted with 50 microliters of elution solution and centrifuged.
Once we had our purified DNA, we measured the concentration. We measured it to be 31.3 ng/microliter. We stored this in the refidgerator for Thursday, when we will electrophorate it.
Tranformation
Decided to Transform E.col: with the F2620 part as back up. We follow this procedure.
(1)105 E.col: calls were added to 100ul BioRad Transformation Solution.
(2)1ul of F2620 DNA from the Registery was added to the cells which were incubated 30min on ice.
(3)Cells were heat shocked by swirling in water at 42 degree water bath for 2min. than return to ice for 30min.
(4)1ml 50B butter was added to the cells and they were incubated for 2 hrs. at room temp.
(5)100ul of the transformed cells were plated on a fresh LB/AMP plate.
