Acid phosphatase staining method for distinguishing malignant serosal cavity effusion mesothelial cells from cancer cells and application thereof
A serosal cavity effusion and acid phosphatase technology, applied in the field of acid phosphatase staining, can solve the problems of difficult cancer cell differentiation, pathologist’s inability to make judgments, and low sensitivity of exfoliated cytology examination, etc. Convenience, reduced workload, guaranteed specificity and sensitivity
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[0012] 1. Acid Phosphatase Staining Kit Components:
[0013] (1) Fixative: 5-10% formalin
[0014] (2) Staining solution: 5-20g / l naphthol AS-BI phosphate dissolved in dimethylformamide
[0015] (3) Fuchsin hydrochloride: 2-10% fuchsin hydrochloride
[0016] (4) Sodium nitrite: 0.1-0.4MNaNO2
[0017] (5) Sodium acetate solution: 2-5M, pH4.5-5.5
[0018] (6) Distilled water
[0019] (7) Nuclear counterstaining solution: 2.5g of hematoxylin, 20ml of absolute alcohol, 5g of potassium aluminum sulfate, 330ml of distilled water, 250mg of sodium iodate, 150ml of glycerol, and 10ml of glacial acetic acid.
[0020] In addition, the above kit may also include an enzyme-labeled liquid-based cytology preservation solution, and its specific composition is as follows:
[0021] (1) 15% Methanol
[0022] (2) 0.1mM EDTA
[0023] (3) 0.1mM NaCl
[0024] (4) 0.01M sodium acetate buffer, pH5.2
[0025] (5) 5% Proclin300
[0026] (6)ddH 2 O.
[0027] 2. Dyeing steps:
[0028] (1) Cel...
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