Template:SBB-Protocols Assay2: Difference between revisions
JCAnderson (talk | contribs) No edit summary |
Simina Ticau (talk | contribs) No edit summary |
||
Line 1: | Line 1: | ||
Checks if cells do/don't bind streptavidin<br> | Checks if cells do/don't bind streptavidin<br> | ||
For all 16 colonies: grow them with/without arabinose to saturation<br> | For all 16 colonies: grow them with/without arabinose to saturation<br> | ||
96 well plate: each well add 300ul PBS, 15ul Streptavidin, 25ul cells <br> | 96 well plate: <br> | ||
- each well add 300ul PBS, 15ul Streptavidin, 25ul cells <br> | |||
- put them at 37C for 30mins-1hour<br> | |||
- check either at room light for red color or UV box for bright white color | |||
<br> | <br> | ||
Controls:<br> | Controls:<br> |
Revision as of 10:23, 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.