Preparation of Agarose Pads for Microscopy of C. elegans
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License | CC Attribution - NoDerivatives 4.0 International: You are free to use, copy, distribute and transmit the work or content in unchanged form for any legal purpose as long as the work is attributed to the author in the manner specified by the author or licensor. | |
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Computer animationProgram flowchartEngineering drawing
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Engineering drawingProgram flowchartBacteriaComputer animation
Transcript: English(auto-generated)
00:01
Preparation of Agarose pads for microscopy of C. elegans. First, pipe at 50 microliters of a 2% Agarose solution on a microscope slide. Then, place a second slide on top and let it stand at room temperature for 5 minutes to harden.
00:28
In the meantime, wash a worm plate with 2 milliliters of M9 buffer to get the worms in suspension.
00:46
Then, pipe at the suspension in an Eppendorf cube and centrifuge for 2 minutes at 5000 g.
01:06
Now, a worm plate is visible at the bottom of the tube. Discard most of the supernatant, but leave a small rest for resuspension.
01:42
Resuspend the worms by flicking against the tube. Now, separate the two Agarose slides and pipe at 10 microliters of worm suspension on the Agarose pad.
02:28
Next, at 10 microliters of a 60 millimolar sodium acid solution to immobilize the worms.
02:46
Finally, place a coverslip on top of the pad. Now, the worms are ready for inspection under the microscope.