Fixed-decalcifying fluid for bone marrow biopsy and paraffin section method of bone marrow biopsy tissue
A technique of biopsy tissue and paraffin section, which is applied in the field of fixation-decalcification solution for bone marrow biopsy and paraffin section of bone marrow biopsy tissue, which can solve the problems of bone marrow biopsy that are not suitable for third-party independent laboratories, and shorten the preparation of specimens. Process, organizational structure is clear, well-preserved effect
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Embodiment 1
[0044] Example 1 Bone marrow biopsy tissue fixation-preparation of decalcification solution
[0045] Based on 1000ml, including
[0046] 0.1M Phosphate Buffer Saline (PBS) 900ml;
[0047] 40% formaldehyde 100ml;
[0048] EDTA 150 g;
[0049] Adjust the pH to 7.0-7.2.
[0050] Wherein, in addition to PBS, other suitable buffers can also be selected as the buffer.
Embodiment 2
[0051] Example 2 Bone marrow biopsy fixation-decalcification method
[0052] The bone marrow biopsy specimen was fixed and decalcified with the fixation-decalcification solution described in Example 1, wherein the volume ratio of sample:fixation-decalcification solution was equal to or greater than 1:10. Fix at room temperature - decalcify for 20-72 hours, then rinse with running water. The fixation and decalcification of the bone marrow tissue in the present invention are accomplished simultaneously in the fixation-decalcification solution.
Embodiment 3
[0053] Example 3 Method for Paraffin Section of Bone Marrow Biopsy
[0054] The specimens of bone marrow biopsy were fixed and decalcified with the fixation-decalcification solution and method described in Example 1 and Example 2 for 20-72 hours, rinsed with running water, dehydrated, soaked in wax, embedded, and sliced (section thickness 2-3 μM ), HE staining and / or immunohistochemical staining, and observed under a microscope. The obtained slices can be directly used for microscope observation and pathological examination, and immunohistochemical staining can also be performed according to different needs. The obtained HE section tissue cells are well preserved and the staining effect is good. The positive immunohistochemical staining was accurately localized, and the background staining was light.
[0055] The dehydration method includes: putting the fixed decalcified bone marrow tissue into formaldehyde for 60 minutes, water for 10 minutes, 75% ethanol for 60 minutes, ...
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