Single-cell slide preparation method based on liquid-based cell slide preparation
A liquid-based cell and single-cell technology, applied in the field of cytology detection, can solve the problems of poor production quality, different thicknesses of smears, and many residual white blood cells and red blood cells, etc., and achieves high stability, good cell fixation, and retention. The effect of cell morphology integrity
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Embodiment 1
[0029] Liquid-based sample processing: put the pretreated liquid-based samples into processing vessels one by one, incubate the liquid-based samples at 37°C, switch the reaction system, wash red blood cells to remove them, change PBS buffer, add magnetic beads to remove white blood cell interference, etc. Treatment; add cell preservation treatment solution; add the liquid-based specimen to the cell preservation treatment solution and shake fully; sedimentation: pour the treated liquid-based sample into the sedimentation chamber, let it settle, and suck off the supernatant; Papanicolaou staining: liquid The basic sample was left to settle, after absorbing the supernatant, put it into absolute ethanol or isopropanol, into pH 7.8 tris buffer, into hematoxylin staining solution, into pH 7.8 tris buffer, Propanol, put in EA-OG mixed dye solution, put in absolute ethanol or isopropanol, repeat 2 times, put in xylene; centrifuge to make slices, transfer the liquid-based sample after P...
Embodiment 2
[0031] In embodiment one, add following operation:
[0032] In step 1, the pretreatment includes liquid-based sample sorting, placement, and code scanning. The incubation time at 37°C is 8-12 minutes. The reaction system is switched to a normal saline system. For 3-5min, remove red blood cells and prepare for subsequent operations.
[0033] Liquid-based sample processing: put the pretreated liquid-based samples into processing vessels one by one, incubate the liquid-based samples at 37°C, switch the reaction system, wash red blood cells to remove them, change PBS buffer, add magnetic beads to remove white blood cell interference, etc. Treatment; add cell preservation treatment solution; add the liquid-based specimen to the cell preservation treatment solution and shake fully; sedimentation: pour the treated liquid-based sample into the sedimentation chamber, let it settle, and suck off the supernatant; Papanicolaou staining: liquid The basic sample was left to settle, after a...
Embodiment 3
[0035] In embodiment two, add following operation:
[0036] In step 2, the cell preservation treatment solution is composed of the following raw materials in parts by weight: 35 parts of ethanol, 3 parts of sodium citrate, 5 parts of sodium chloride, 7 parts of N-acetylcysteine, 6 parts of dithiothreitol 3 parts of proline, the volume ratio of liquid-based specimens and cell preservation treatment solution is 1:3, which can remove red blood cells in liquid-based specimens and fix the original form of cells with diagnostic value in time; for mucus and epidermal tissue Softening and degradation are performed to separate effective cells from the mucus.
[0037] Liquid-based sample processing: put the pretreated liquid-based samples into processing vessels one by one, incubate the liquid-based samples at 37°C, switch the reaction system, wash red blood cells to remove them, change PBS buffer, add magnetic beads to remove white blood cell interference, etc. Treatment; add cell pre...
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