Paraffin-embedded tissue sample processing method and kit for tumor prognosis evaluation
A paraffin-embedded, prognostic assessment technology, applied in the field of pathological diagnosis, can solve problems such as different risk levels and cannot be dynamically explained, and achieve the effect of improving accuracy, efficiency and accuracy
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Embodiment 1
[0069] Example 1 Making the flow of cell nuclear monolays in a variety of paraffin-embedded tissue samples
[0070] The production process of the nuclear monocyclic dyeing smear in this embodiment is like figure 1 As shown, the specifically can include the following steps:
[0071] The tissue sections of tumor enrichment 50 μm thickness were obtained from paraffin-embedded tumor tissue samples, and after dewaxing, rinsing, digestion, screen filtration, centrifugal, filtration, and preparing nuclear single layers;
[0072] The nucleus is hydrolyzed in the nucleus of the nucleus, and then the nucleus is soaked with the nucleus and eluted with the eluate, and then dehydrated, encapsulated, and the dyed nuclear monochride smear was obtained.
Embodiment 2
[0073] Example 2 Extraction of Sample Calcotids of Paraffled Buried Tissue
[0074] This embodiment uses a kit or a nuclear extracting kit for a paraffin-embedded tissue sample treatment method for tumor prognosis, which contains at least:
[0075]
[0076] The amount of the above reagents can be extracted from 5 sample extraction. The kit can be transported at 2-8 ° C, and the lysase is stored in -20 ± 5 ° C, and other reagents are stored at room temperature, and the effective phase of the kit is 18 months.
[0077] The kit may also include a supplies: 5 nylon cell sieve (aperture 60 μm), 5 sheets of filter paper (aperture diameter, 10 magnetic stirrer, 2 black paper jam, 5 boron silicon small glass bottles (10ml), 5, 10 pieces of boron silicon slides, centrifuge (15 ml).
[0078] The steps of nuclear extraction are as follows:
[0079] 2.1 Slices
[0080] 2 tablets of 50 μm thick paraffin bury tissue sections, the slice is not too thin or too thick, the thin fragment is large,...
Embodiment 3
[0105] Example 3 Cell nuclear monochacolate DNA dyeing
[0106] This embodiment uses a kit or a nuclear monoqueric smear DNA dyeing kit for a paraffin coated tissue sample treatment method for tumor prognosis, which contains at least:
[0107]
[0108] The amount of the above reagents can be stained with 5 pieces of smear. The kit can be transported at 2-8 ° C, and the DNA dyed liquid is preserved at 2-8 ° C, and other reagents are stored at normal temperature, and the effective phase of the kit is 18 months.
[0109] The kit can also include a reagent: 70% ethanol solution, 95% ethanol solution, anhydrous ethanol, xylene, Eukitt sealing agent.
[0110] The kit can also include a consumable: tin paper, 1 size of 30 cm × 30 cm, and the other 5 is 7 cm × 7 cm.
[0111] The steps of nuclear staining are as follows:
[0112] 3.1 Acid hydrolysis
[0113] 3.1.1 Transfer the nuclear single-layer slide of the previously fixed liquid to the glass dyeing tank, slowly rinse with the tap wa...
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