IGEM:The Citadel/Notebook/Notes Patrick: Difference between revisions
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Replated BBa_I20260<br> | Replated BBa_I20260<br> | ||
Placed into incubator and 9:59am. | Placed into incubator and 9:59am. | ||
== Wednesday, July 08, 2010== | |||
===9:30am=== | |||
Worked on theory for most of morning and afternoon. | |||
===2:00pm=== | |||
Inoculated 80μL of LB-Miller (Amp) broth with following parts and placed into incubator.<br> | |||
I13521<br> | |||
J23101<br> | |||
J45120<br> | |||
I0462<br> | |||
I20260<br> | |||
(Cultures will be removed tomorrow morning and added to 40μL of glycerol(50%) and stored at -80°C.)<br> |
Revision as of 12:12, 8 July 2010
Friday, June 25, 2010
11:14am
Removed inoculated conical tubes from yesterday from incubator.
Removed the following plates from yesterday from incubator and placed into 4°C.
Agar in some plates was deformed and not completely dry
KEPT THE FOLLOWING PLATES (Listed according to quality of gel, not necessarily colony formation):
BBa_F1610 [100%]
- Completely dry.
- Many cells, one large cluster.
BBa_J45120 [100%]
- Completely dry.
- Many cells. Some formation along rim of agar.
BBa_R0063 [25%]
- Completely dry.
- Average colonies.
BBa_R0063 [25%]
- Completely dry.
- Average colonies.
BBa_R0040 [25%]
- Almost completely dry.
- Very few colonies.
BBa_F2620 [25%]
- Completely dry.
- Few colonies, but good ones.
BBa_F1610 [50%]
- Completely dry.
- Normal colonies.
BBa_E0240 [50%]
- Completely dry.
- Very few colonies. Colonies along rim.
BBa_I0462 [100%]
- Some liquid. Some agar on cover.
- Many colonies.
BBa_I0462 [50%]
- Some liquid.
- Normal/average colonies.
BBa_I0462 [25%]
- Slightly more liquid. Liquid agar on 1/2 of rim circumferance.
- Few colonies. Colonies along rim.
BBa_F2620 [50%]
- Liquid agar on 1/3 of rim.
- Average colonies.
BBa_J45120 [25%]
- Few colonies. Small colonies. Bacterial smear covering 1/12 of plate.
BBa_C0160 [25%]
- Liquid agar on 1/2 of rim.
- Very few colonies, but good ones.
BBa_B0015 [25%]
- Liquid agar on entire rim.
- Average colony formation.
DISCARDED THE FOLLOWING PLATES
BBa_J45200 [25%]
- Too much liquid agar on cover. Unsolidified gel.
- No visible colonies.
BBa_C0160 [50%]
- Too much liquid agar on cover. Unsolidified gel.
- Irregular colony formation across unsolidified gel.
BBa_B0015 [50%]
- Completely unsolidified gel.
- Bacteria formation on cover. Irregular colonies.
BBa_J45120 [50%]
- Too much liquid agar on cover. Unstable gel.
- Carpet style formation of bacteria.
BBa_J23102 [50%]
- Too much liquid agar on cover. Unstable gel.
- Bacteria formation on cover.
BBa_J45200 [50%]
- Too much liquid agar on cover. Unsolidified gel.
- No visible colonies.
BBa_R0062 [50%]
- Too much liquid agar on cover. Unstable gel.
- Carpet style formation of bacteria.
BBa_R0062 [50%]
- Agar dripping onto cover, taking colony formations with it.
BBa_E0240 [25%]
- Completely dry. Agar slightly unstable.
- Would be difficult to isolate from.
NOTES
Need to replate BBa_J45200 [25%], [50%].
Need to replate BBa_J23102 [25%], [50%].
Need to replate BBa_B0015 [50%].
Need to replate BBa_C0160 [50%].
Need to replate BBa_R0062 [25%], [50%].
Need to replate BBa_J4512 [50%].
Need to replate BBa_E0240 [25%].
In the future:
- Do not reheat agar solution in water bath during plate pouring.
- Ensure that plates have adequate time to dry completely.
12:45pm
Prepare LB-Miller (Amp) broth for x24 5mL liquid cultures
Prepare LB-Miller (Amp) agar 500mL
- Therefore, use total 1.24mL Amp (50μL/mL stock)
1:55pm
Plated BBa_I20260 [100%], [50%], [25%] Placed plates into 37°C incubator.
Tuesday, June 29, 2010
~12:30pm
Streak plated from isolations of the following parts and placed into incubator:
BBa_R0063
BBa_I20260
~3:00pm
Poured 33 LB-Miller (Kan) plates and 13 LB-Miller (Amp) plates
4:33pm
Inoculated the following and placed into incubator for miniprep tomorrow morning:
BBa_I20260 in 5mL LB Miller (Kan) broth
BBa_J45120 in 5mL LB Miller (Amp) broth
BBa_I0462 in 5mL LB Miller (Amp) broth
Wednesday, June 30, 2010
9:45am
Yesterday's plating of BBa_I20260 failed.
Replated BBa_I20260
Placed into incubator and 9:59am.
Wednesday, July 08, 2010
9:30am
Worked on theory for most of morning and afternoon.
2:00pm
Inoculated 80μL of LB-Miller (Amp) broth with following parts and placed into incubator.
I13521
J23101
J45120
I0462
I20260
(Cultures will be removed tomorrow morning and added to 40μL of glycerol(50%) and stored at -80°C.)