Template:SBB-Protocols Assay2: Difference between revisions
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- put them at 37C for 30mins-1hour<br> | - put them at 37C for 30mins-1hour<br> | ||
- check either at room light for red color or UV box for bright white color | - check either at room light for red color or UV box for bright white color | ||
<br> | <br><br> | ||
Controls:<br> | Controls:<br> | ||
pBca9145-Bca 9494 (positive control that displays cpx, a streptavidin binding peptide under Pbad)<br> | pBca9145-Bca 9494 (positive control that displays cpx, a streptavidin binding peptide under Pbad)<br> |
Revision as of 10:25, 20 April 2009
Checks if cells do/don't bind streptavidin
For all 16 colonies: grow them with/without arabinose to saturation
96 well plate:
- each well add 300ul PBS, 15ul Streptavidin, 25ul cells
- put them at 37C for 30mins-1hour
- check either at room light for red color or UV box for bright white color
Controls:
pBca9145-Bca 9494 (positive control that displays cpx, a streptavidin binding peptide under Pbad)
DH10B (no plasmid, negative control)
pBca9495CA-Bca1144 (negative control: backbone)
Can play with:
- streptavidin concentrations
- mid-log vs. saturation
- quantitative assays (number of washes, volume...)
JCA: This needs much more detail. In particular, write up the details about the volumes of materials, composition of the assays, times and temperatures at each step, etc.