Mounting Adult Drosophila Brains: A Method to Prepare Slides for Confocal Imaging
成績單
– On a positively-charged microscope slide, adhere two cover slips with enough distance between them 到 create a space for the Drosophila brains 到 be mounted. Under the stereo microscope, pipette the brains in mounting medium into that space. The negative charge of the tissue will help the brains adhere 到 the positive charge on the surface of the slide.
Remove excess mounting medium 到 allow for precise positioning of the brains on the slide in a grid pattern with the antennal lobes facing up, then bridge the two cover slips by adhering a third cover slip across 到 cover the brains.
To fill in the cavity, place mounting medium one drop at a time into the edge of the cavity, and allow it 到 spread by capillary motion so that it does not disturb the brains.
Seal the cavity with nail polish, and store at negative 20 degrees Celsius in the dark 到 preserve the fluorescence of stained tissues.
In the example protocol, we will mount Drosophila brains for confocal imaging of immunostained neurons.
– To mount the brains, build a bridge slide. Position two base covers slips roughly one centimeter apart on a positively-charged slide. Make certain that the positively-charged side is face up. Then adhere the cover slips 到 the slide with fingernail polish, and let the polish dry completely before proceeding.
Next, place the slide under a stereo microscope and pipette brains in medium into the space between the cover slips. Be sure 到 adjust the lighting 到 improve visualization of the brains.
Next, aspirate the extra mounting media from the slide, being careful 到 avoid the brains. Then, wick away remaining excess mounting media. This will allow the brains 到 be positioned more precisely. Now, using forceps, orient the brains into a grid pattern with their antennal lobes facing up.
Then, place a cover slip over the brains, and use fingernail polish 到 seal the edges of the top cover slip that are attached 到 the base cover slips.
Now, load the center cavity with fresh mounting media drop-wise, allowing the media 到 be drawn under the cover slip by capillary action. When the cavity is filled, seal it in completely using clear fingernail polish.
