Staining kit and staining method, use thereof
A dyeing reagent and dyeing method technology, applied to the dyeing kit and its dyeing and application fields, can solve the problems of difficult popularization, time-consuming separation and culture method, and insufficient standardization of micro-immunofluorescence method, and achieve the effect of many inspection items.
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Embodiment 1
[0033] Get 50% dehydrated methanol and 50% dehydrated ethanol (volume percentage) after adding in equal amounts as the fixative;
[0034] Put 1.5g of Wright's powder and 1.5g of Giemsa's powder together in a clean mortar, add a small amount of methanol to fully grind, absorb the upper layer, then add a small amount of methanol, continue grinding, and then absorb the upper layer, and so on. Several times, until the internal dye in the mortar is fully dissolved and washed, put it into a brown glass bottle, add 0.6g of Azure II, 100ml of glycerin, and make up methanol to 900ml as a staining solution. Shake well once a day for a total of one week, store for another week, filter, and store in a brown ground glass bottle for later use.
[0035] Take 7 g of anhydrous potassium dihydrogen phosphate, 3 g of anhydrous disodium hydrogen phosphate, add 1000 ml of distilled water as a differentiation solution, and adjust the pH value to pH 6.8 with phosphate.
[0036] The kit consists of ...
Embodiment 2
[0038] Put 6 drops of fixative solution on the cervical smear, fix it for 20 seconds, and pour off the fixative solution by moving the slide sideways. Add 2 drops of staining solution, spread the staining solution over the specimen, and dye for 5 seconds. Immediately add 8 drops of differentiation solution, gently rotate the slide to mix it with the staining solution, and differentiate for 38 seconds. Use small running water to slowly buffer off the residual liquid and its sediment, wipe off the moisture on the back of the slide, and examine the wet slide.
[0039] Note: 1. The mouth of the bottle must be pierced with a needle before use, so that the dye solution can drip out smoothly. 2. When scraping (smearing) slices, the position should be appropriate, the sample should be sufficient, the technique should be light, and the smear should be thin. Too few specimens are often the main reason for missed diagnosis. 3. The dyeing time can be appropriately extended according to...
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