A Method for Effectively Improving the Excision Rate of Parathyroid Histopathological Slices in Experimental Animals
A parathyroid and experimental animal technology, applied in the preparation of test samples, sampling devices, etc., can solve problems such as affecting test quality, inability to cut out parathyroid tissue, and loss of parathyroid tissue.
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Embodiment 1
[0028] Embodiment 1 hematoxylin staining method
[0029] The fixed thyroid gland was wiped dry with dust-free paper to check the location of the parathyroid glands. The tip of the toothpick was blunted and dipped in hematoxylin solution for staining to stain the parathyroid glands. After the hematoxylin solution was dry, it was dehydrated together with other tissues. When embedding, embed the parts with hematoxylin color on both sides at the same horizontal position. When slicing, the tissue should be roughly trimmed, and carefully observed when it is close to the site marked by hematoxylin, and sliced after the parathyroid glands are trimmed out.
Embodiment 2
[0030] Example 2 Comparative study of hematoxylin-labeled parathyroid glands and traditional film-making methods
[0031] Research method: Thyroid and parathyroid gland tissues of 250 rats were randomly prepared by 5 methods. The production process of the conventional method is as follows: the parathyroid glands together with the thyroid are taken out → 10% neutral formalin fixation → dehydration → paraffin embedding → sectioning → staining. Hematoxylin solution 1-4 labeling method The production process is as follows: take out the parathyroid gland together with the thyroid gland → 10% neutral formalin fixation → label the parathyroid gland with hematoxylin solution 1 → dehydration → paraffin embedding → sectioning → staining; Parathyroid glands were taken out together with the thyroid → 10% neutral formalin fixation → hematoxylin solution 2 labeled parathyroid glands → dehydration → paraffin embedding → sectioning → staining; parathyroid glands were taken out together with t...
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