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Harvard BioDesign/8 July 2014
From 2014.igem.org
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Picked colonies from PCR of pHBD39-41 to clone out prefix. Only pHBD41 had many colonies. Picked 2 colonies from pHBD41 and one colony from pHBD40 to grow up for miniprep. (We forgot to do this miniprep that day). | Picked colonies from PCR of pHBD39-41 to clone out prefix. Only pHBD41 had many colonies. Picked 2 colonies from pHBD41 and one colony from pHBD40 to grow up for miniprep. (We forgot to do this miniprep that day). | ||
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Heat Shock Promoter Assay: | Heat Shock Promoter Assay: | ||
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Heat shock for 10 minutes at 25C-37C-42C | Heat shock for 10 minutes at 25C-37C-42C | ||
Take 100uL into well of 96 well plate and take measurements in plate reader every 15 minutes for 6 hours. | Take 100uL into well of 96 well plate and take measurements in plate reader every 15 minutes for 6 hours. | ||
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Transformed pHBD41 and 43 (blue and yellow chromoprotein) into LSR10 cells. | Transformed pHBD41 and 43 (blue and yellow chromoprotein) into LSR10 cells. | ||
| - | 15: | + | 15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)[[User:Mmmlong|Mmmlong]] |
Plated LSR10 and Turbo cells from biocompatibility assay | Plated LSR10 and Turbo cells from biocompatibility assay | ||
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5 microliters of water | 5 microliters of water | ||
10 microliters master mix | 10 microliters master mix | ||
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Ran gel on plasmids resulting from Gibson | Ran gel on plasmids resulting from Gibson | ||
Latest revision as of 20:21, 17 October 2014
Gel extracted parts for HybB + SB3K3 for Gibson. Ran Gibson. Transformed.
Picked colonies from PCR of pHBD39-41 to clone out prefix. Only pHBD41 had many colonies. Picked 2 colonies from pHBD41 and one colony from pHBD40 to grow up for miniprep. (We forgot to do this miniprep that day).
Heat Shock Promoter Assay:
Put 20uL of pHBD26 which was grown up overnight in 10mL media into 1mL of LB
Approach 1:
In 3 replicates:
Incubate shaking for 1, 2, 3, 4, 5, & 6 hours at 25C-37C-42C Inoculate 3 samples with just cells right before read Take 100uL of each into well of 96-well plate and take measurements in plate reader
Approach 2:
In duplicates:
Heat shock for 10 minutes at 25C-37C-42C Take 100uL into well of 96 well plate and take measurements in plate reader every 15 minutes for 6 hours.
Transformed pHBD41 and 43 (blue and yellow chromoprotein) into LSR10 cells.
15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)15:21, 17 October 2014 (CDT)Mmmlong
Plated LSR10 and Turbo cells from biocompatibility assay Plated LSR10, with autoclaved paint components (2) Plated LSR10, with non-autoclaved paint components (1) Plated Turbo with autoclaved paint components
Performed Gibson reaction Used gblock inserts and linearized F12 backbone 4 microliter of insert to Gibson (0.1 pmol) 4 microliters of backbone to Gibson (0.03 pmol) 5 microliters of water 10 microliters master mix
Ran gel on plasmids resulting from Gibson Bands were a little over 4,000 base pairs Backbone is around 4,000 bp Inserts were 35-45 bp long Gel extracted plasmids
