Preparation method of cell wax block on the basis of bloody cell specimen and the cell wax block
A cell wax block and sample technology, applied in the biological field, can solve the problems of affecting the quality of the wax block, affecting the diagnosis result, and long fixation time, etc., to achieve the effects of preventing interference, improving accuracy, and improving enrichment
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Embodiment 1
[0043] A kind of cell wax block, it is made by following preparation method:
[0044]After the blood cell sample was washed with the first fixative solution, centrifuged for the first time at 3000r / min for 5min, and after standing for 10min, the precipitate and the supernatant 1cm away from the precipitate were collected, dispersed, and again at 3000r / min Centrifuge for 5 minutes under the condition of 3000r / min, discard the supernatant, collect the first precipitate sample, add the second fixative, mix evenly, and centrifuge for the second time under the condition of 3000r / min for 5min to obtain the second precipitate, dehydrate the second precipitate, and make it transparent , soaked in wax, embedded, and cut the embedded blood cell sample into thin slices with a thickness of 4um.
[0045] Wherein, the first fixative solution is ethanol acetic acid solution, and the ethanol acetic acid solution is obtained by mixing ethanol with a volume fraction of 25% and acetic acid at a ...
Embodiment 2
[0051] A kind of cell wax block, it is made by following preparation method:
[0052] Let the blood cell sample stand overnight, take the bottom 20ml blood cell sample and wash it with the first fixative, centrifuge for the first time at 3100r / min for 5min, collect the first sediment sample, add the second fixative, mix well Finally, centrifuge for the second time under the condition of 3100r / min for 5min to obtain the second precipitate. The second precipitate is dehydrated, transparent, soaked in wax, embedded, and the embedded blood cell sample is cut into thin slices with a thickness of 5um.
[0053] Wherein, the first fixative solution is ethanol acetic acid solution, and the ethanol acetic acid solution is obtained by mixing ethanol with a volume fraction of 25.5% and acetic acid at a volume ratio of 19:1.
[0054] The second fixative solution is a neutral buffered formaldehyde solution with a concentration of 3.5 wt% at a temperature of 4.5°C.
[0055] Dehydration incl...
Embodiment 3
[0059] A kind of cell wax block, it is made by following preparation method:
[0060] Let the blood cell sample stand overnight, take the bottom 30ml blood cell sample and wash it with the first fixative, centrifuge for the first time at 3100r / min for 6min, collect the first sediment sample, add the second fixative, mix well Finally, centrifuge for the second time under the condition of 2900r / min for 6min to obtain the second precipitate. The second precipitate is dehydrated, transparent, soaked in wax, embedded, and the embedded blood cell sample is cut into thin slices with a thickness of 3um.
[0061] Wherein, the first fixative solution is ethanol acetic acid solution, and the ethanol acetic acid solution is obtained by mixing ethanol with a volume fraction of 25.5% and acetic acid at a volume ratio of 18:1.
[0062] The second fixative solution is a neutral buffered formaldehyde solution with a concentration of 4 wt% at a temperature of 3.5°C.
[0063] Dehydration includ...
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