Method for improving image signal-to-noise ratio by using water-soluble light absorbent
A light absorber and water-soluble technology, applied in the field of using water-soluble light absorbers to improve the image signal-to-noise ratio, can solve the problems of slow imaging speed, poor maintenance, unfavorable shape, etc.
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example 1
[0047] Example 1 Fluorescent protein labeled mouse brain tissue samples
[0048] Step 1: Inject a mixture of 10% urethane and 2% chloral hydrate into the abdominal cavity of two-month-old Thy1-GFP male mice for anesthesia, perfusion to take the brain, fixation with PFA for 24 hours, and rinse with PBS for 24 hours;
[0049] Step two, slice the whole mouse brain on a vibrating microtome for 200-500um;
[0050] Step 3: Dissolve a certain concentration of water-soluble light absorber in PBS, and put the sliced brain slices into PBS-water-soluble light absorber solution (the mass concentration of water-soluble light absorber is 0.1%-5%) and penetrate 0.1-10h, use Keyamine as water-soluble light absorber TM Black SP-IJ Liquid;
[0051] Step 4: Mount the infiltrated brain slice and image it on a fluorescence microscope. A wide-field fluorescence microscope can be used;
[0052] by Figure 1 ~ Figure 4 It can be seen from the content shown that after the light absorber-PBS solution is used ...
example 2
[0053] Example 2 Dye-labeled mouse brain tissue samples
[0054] Step 1: Inject DyLight 488 into the tail vein of two-month-old C57 male mice. After 20 minutes, they were injected with a mixture of 10% urethane and 2% chloral hydrate for anesthesia. The brain was taken out by perfusion, fixed with PFA for 24 hours, and rinsed with PBS for 24 hours;
[0055] Step two, slice the whole mouse brain for 200-500μm on a Leica commercial vibrating microtome;
[0056] Step 3: Dissolve a certain concentration of water-soluble light absorber in PBS, and put the sliced brain slices into PBS-water-soluble light absorber solution (the mass concentration of water-soluble light absorber is 0.1%-5%) and penetrate 0.1-10h, water-soluble light absorber selected from Keyamine TM Black SP-IJ Liquid;
[0057] Step 4: Mount the infiltrated brain slice and image it on a fluorescence microscope;
[0058] by Figure 5 ~ Figure 7 From the content shown, it can be seen that before and after using the light abs...
example 3
[0059] Example 3 Dye-labeled mouse kidney samples
[0060] Step 1: Inject DyLight 488 into the tail vein of two-month-old C57 male mice. After 20 minutes, they were injected with a mixture of 10% urethane and 2% chloral hydrate for anesthesia. Kidneys were taken by perfusion, fixed with PFA for 24 hours, and rinsed with PBS for 24 hours;
[0061] Step 2: Embed the mouse kidney with agarose and slice it 200-500μm on the Lycra commercial vibrating microtome;
[0062] Step 3: Dissolve a certain concentration of water-soluble light absorber in PBS, and put the cut kidney tissue into PBS-water-soluble light absorber solution (the mass concentration of water-soluble light absorber is 0.1%-5%) to penetrate 0.1-10h, water-soluble light absorber selected from Keyamine TM Black SP-IJ Liquid;
[0063] Step 4: Mount the infiltrated kidney tissue and image it on a fluorescence microscope;
[0064] by Picture 8 From the content shown, it can be seen that before and after using the light absorber, t...
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