Team:Alberta/Plates
From 2010.igem.org
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==29-06-10== | ==29-06-10== | ||
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- | :1) Approximately | + | :1) Followed procedure from June 26, 2010 to put new LB agar into the L.B.O. tube |
- | + | :2) Approximately 1cm was sliced off the top of the new LB agar with an ethanol-sterilized razor blade | |
:3) L.B.O. stick was incubated overnight at 37C | :3) L.B.O. stick was incubated overnight at 37C | ||
Observations: | Observations: | ||
- | : - | + | : - no growth observed, tube must have been sterile |
- | : - distinct E.coli smell | + | |
+ | |||
+ | ==30-06-10== | ||
+ | :1) Streaked green colony from a plate of Cambridge parts | ||
+ | :2) L.B.O. stick was incubated overnight at 37C | ||
+ | |||
+ | Observations: | ||
+ | : - green streak and individual green colonies observed, along with a distinct E.coli smell | ||
+ | |||
+ | ==05-07-10== | ||
+ | :1) Approximately 1cm was sliced off the top of the used LB agar with an ethanol-sterilized razor blade | ||
+ | :2) Streaked red, RFP-containing colony onto the LB agar surface. | ||
+ | :3) L.B.O. stick was incubated overnight at 37C | ||
+ | |||
+ | Observations: | ||
+ | : - only a red streak and individual red colonies observed, along with a distinct E.coli smell | ||
+ | : - no remnants of green colonies visible |
Revision as of 18:53, 16 July 2010
Notebook | Building Parts | Testing Parts | Assembly Method | Competent Cells | Plates | Kit Manual | Software |
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Plates
L.B.O.
24-06-10
Creation of "L.B.O.": a deodorant stick of LB agar
All of the following steps were performed in a safety cabinet under sterile conditions.
- 1) disassembled a Degree deodorant stick and soaked in ethanol
- 2) removed the raising platform and covered it with Parafilm
- 3) coated the insides of the tube with mineral oil
- 5) removed platform and poured LB agar into the base of the stick, waited until it solidified
- 6) the Parafilmed platform was put back into the stick and lowered maximally
- 7) LB agar was poured on top of the platform, until the tube was full, waited until it solidifed
- 8) The top of the LB agar was sliced off with an ethanol-sterilized knife
- 9) 400ul of transformed competent cells were plated on the stick as if it was a standard LB agar plate
- 10) L.B.O. stick was incubated overnight at 37C
- - although the knife cut through the LB agar easily, it was difficult to produce a completely flat surface
- - solidified LB agar was effectively raised and lowered using the dial
- - after incubation, a bacterial lawn was observed and a distinct E.coli smell was present
29-06-10
- 1) Followed procedure from June 26, 2010 to put new LB agar into the L.B.O. tube
- 2) Approximately 1cm was sliced off the top of the new LB agar with an ethanol-sterilized razor blade
- 3) L.B.O. stick was incubated overnight at 37C
Observations:
- - no growth observed, tube must have been sterile
30-06-10
- 1) Streaked green colony from a plate of Cambridge parts
- 2) L.B.O. stick was incubated overnight at 37C
Observations:
- - green streak and individual green colonies observed, along with a distinct E.coli smell
05-07-10
- 1) Approximately 1cm was sliced off the top of the used LB agar with an ethanol-sterilized razor blade
- 2) Streaked red, RFP-containing colony onto the LB agar surface.
- 3) L.B.O. stick was incubated overnight at 37C
Observations:
- - only a red streak and individual red colonies observed, along with a distinct E.coli smell
- - no remnants of green colonies visible