Bologna University/Fluorescence Test

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::1. Growth O/N for 15h in LB (5ml) of:
::1. Growth O/N for 15h in LB (5ml) of:
-
::::-transformed E. Coli with appropriate antibiotic;
+
::::-transformed E. coli with appropriate antibiotic;
-
::::-E. Coli.
+
::::-E. coli.
-
::2. '''All measures have to be done in M9 with OD=1.2.'''
+
::2. '''All measures must be done in M9 with OD=1.2.'''
-
::3. The day after in the morning measure OD.
+
::3. The day after, in the morning, measure OD.
::4. To obtain OD=1.2:
::4. To obtain OD=1.2:
-
::::-centrifugate 4ml of bacteria culture at 4400rpm for 3min at 25°C;
+
::::-centrifuge 4ml of bacterial culture at 4400rpm for 3min at 25°C;
::::-discard the supernatant;
::::-discard the supernatant;
-
::::-resuspende cell pellet in 6ml of M9 medium with glucose and appropriate antibiotic (1000x).
+
::::-resuspend the cell pellet in 6ml of M9 medium with glucose and appropriate antibiotic (1000x [ ]).
-
::5. Measure OD: adjust OD to 1 through further diluition or growth.
+
::5. Measure OD: adjust OD to 1.2 through further dilution or cell growth.
::6. Adjust PMT offset with untransformed E. Coli.
::6. Adjust PMT offset with untransformed E. Coli.
::7. Test culture fluorescence before IPTG induction.
::7. Test culture fluorescence before IPTG induction.
Line 17: Line 17:
::::-centrifugate bacteria culture at 4400rpm for 3min at 25°C;
::::-centrifugate bacteria culture at 4400rpm for 3min at 25°C;
::::-discard the supernatant;
::::-discard the supernatant;
-
::::-resuspende cell pellet in M9 medium and 2mM IPTG with appropriate antibiotic (1000X);
+
::::-resuspend cell pellet in M9 medium and 2mM IPTG with appropriate antibiotic (1000x [ ]);
::9. Incubate at 37°C.
::9. Incubate at 37°C.
::10. Test fluorescence after 10min, 20min, 30min, 1h, 2h.
::10. Test fluorescence after 10min, 20min, 30min, 1h, 2h.
[[Bologna University/Protocols | Back]]
[[Bologna University/Protocols | Back]]

Latest revision as of 09:34, 25 October 2007

1. Growth O/N for 15h in LB (5ml) of:
-transformed E. coli with appropriate antibiotic;
-E. coli.
2. All measures must be done in M9 with OD=1.2.
3. The day after, in the morning, measure OD.
4. To obtain OD=1.2:
-centrifuge 4ml of bacterial culture at 4400rpm for 3min at 25°C;
-discard the supernatant;
-resuspend the cell pellet in 6ml of M9 medium with glucose and appropriate antibiotic (1000x [ ]).
5. Measure OD: adjust OD to 1.2 through further dilution or cell growth.
6. Adjust PMT offset with untransformed E. Coli.
7. Test culture fluorescence before IPTG induction.
8. IPTG induction:
-centrifugate bacteria culture at 4400rpm for 3min at 25°C;
-discard the supernatant;
-resuspend cell pellet in M9 medium and 2mM IPTG with appropriate antibiotic (1000x [ ]);
9. Incubate at 37°C.
10. Test fluorescence after 10min, 20min, 30min, 1h, 2h.

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