Difference between revisions of "20210326 3Dcell labnotes"
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== Pressure control of gel == | == Pressure control of gel == | ||
| + | * Set up gel preparation for small amounts of agarose gel (~0.5 ml) | ||
| + | * For other gels this can work with even smaller amounts of fluid | ||
| + | * When gel is ready the pressure input (needle) and fluid output (tube) is glued to gas tighten with UV glue | ||
| + | * Small ID tubing assures little waste of gel | ||
| + | * Even | ||
| + | [[File:Sample holder and chip on microscope.jpg|left|thumb|Sample holder and chip on microscope]] | ||
| + | [[File:PC screen and microscope.jpg|left|thumb|PC screen with image of circuit and microscope]] | ||
| + | [[File:P&T controllers + UV lamp.jpg|left|thumb|P&T controllers + UV lamp]] | ||
| + | [[File:Weighing directly in Eppendorf.jpg|left|thumb|Weighing directly in Eppendorf]] | ||
| + | [[File:Heating Eppendorf to dissolve agar in DIW.jpg|left|thumb|Heating Eppendorf to dissolve agar in DIW]] | ||
Revision as of 17:17, 26 March 2021
Pressure control of gel
- Set up gel preparation for small amounts of agarose gel (~0.5 ml)
- For other gels this can work with even smaller amounts of fluid
- When gel is ready the pressure input (needle) and fluid output (tube) is glued to gas tighten with UV glue
- Small ID tubing assures little waste of gel
- Even
