Improved histiocyte staining method and application thereof
A staining method and cell technology, applied in the preparation of test samples, etc., can solve the problems of high false positive rate and false negative rate of Papanicolaou staining
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Embodiment 1
[0102] Example 1 Fixed
[0103] regular fixed :
[0104] Fix the smear (when wet) in 95% alcohol or an equal mixture of 95% alcohol and ether for at least 15 minutes.
[0105] Place them in 80%, 70%, and 50% alcohol for half a minute. Then put in and distilled water for more than 2 minutes.
[0106] special fixative
[0107] Specimen smear fixation: take 7.5ml A solution and 42.5ml B solution and mix to form a special fixative solution. Quickly put the specimen smear into the fixative solution for 50 seconds, take it out and immediately rinse it up and down 10 times in a purified water tank. Can be stored in the refrigerator at 4°C for 2 weeks.
Embodiment 2
[0108] Example 2 Dyeing
[0109] 1. Traditional Pap staining steps
[0110] (1) Stain the fixed sample smear with hematoxylin for 5-10 minutes until the nucleus coloring is obvious, and then rinse it with distilled water.
[0111] (2) Use 0.25% or 0.5% hydrochloric acid alcohol to remove excess hematoxylin in the cytoplasm, until the smear turns light red, rinse it with distilled water immediately, and the operation must be rapid, usually within a few seconds. If the decolorization time is too long, all the hematoxylin will disappear.
[0112] (3) Alkaline in a saturated lithium carbonate solution for about 1 minute until the smear turns light blue, then wash with distilled water.
[0113] (4) Place them in 50%, 70%, and 80% alcohol for half a minute. Then place in 95% alcohol for at least 2 minutes to dehydrate.
[0114] (5) Dye in orange G-6 staining solution for 3 minutes.
[0115] (6) Rinse up and down 6 times in two 95% alcohol tanks respectively.
[0116] (7) Dye i...
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