
Gill's II Hematoxylin Stain
Please be advised that the price mentioned above is only for your reference. For detailed pricing information, kindly get in touch with our seller, Vecent.
Description
| SKU-Pack Size | Availability | Price |
| abs9219-100ml | 1-2weeks | $40.00 |
| abs9219-500ml | 1-2weeks | $170.00 |
Please be advised that the price mentioned above is only for your reference. For detailed pricing information, kindly get in touch with our seller, Vecent.
Description | |
| Description | Gill's I, II, and III are all cytological stains, but with differing levels of progressiveness or regressiveness depending on their duration of application. These stains work by binding the positively charged aluminum-oxyhematoxylin complex to the negatively charged phosphate group of nuclear DNA, resulting in a vivid blue-purple coloration. Hematoxylin staining is a widely used technique in cytology and histology for highlighting cellular and nuclear structures of interest. |
| Usage | Here is a rearranged version of the original text content: To prepare the smear, it was first fixed in 95% ethanol for 15 minutes. Then, it was gently rinsed with running water for 30 seconds. Next, the smear was stained with Gill's II hematoxylin solution for a period of 1.5 to 3 minutes. After staining, it was rinsed again with running water. In the next step, the smear was rinsed in either Scott's Tap Water Substitute (BF058) or warm slightly alkaline tap water or diluted ammonia for 15 to 60 seconds. Following this, another rinse with running water was done. To enhance the staining, the smear was dipped in 95% denatured alcohol (BF057) or 95% ethanol for 10 times. Subsequently, it was redyed with Pasteurized solution OG (ST017) for 1.5 minutes. The smear was then again dipped in 95% denatured alcohol or ethanol for 10 times, repeated twice. Continuing the staining process, it was redyed with Pasteurized dye EA (ST017) for a period of 2.5 to 3 minutes and dipped in 95% denatured alcohol or ethanol for 10 times, repeated twice. After that, the smear was rinsed in anhydrous ethanol for 1 minute, repeated twice. Finally, it underwent rinsing in xylene or xylene substitute for 2 minutes, repeated twice, before microscopic examination after cover. For regression staining, the frozen sections underwent dewaxing and hydration. Then, they were stained with Gill's II hematoxylin for a period of 1.5 to 3 minutes. Following staining, the sections were rinsed with running water. A differentiation solution was applied for 20 to 60 seconds, followed by another rinse with running water. To complete the staining process, the sections were rinsed in either Scott's Tap Water Substitute, warm slightly alkaline tap water, or diluted ammonia for 15 to 60 seconds. After a final rinse with running water, the staining procedure differed based on the purpose. For histology, the sections were restained with Eosin Y (alcohol soluble or water soluble) for 30 to 60 seconds. For cytology, restaining was done with Pasteurized solution OG or EA (ST017) for a period of 1 to 3 minutes. Dehydration, transparency, tablet sealing, and microscopic examination followed for both cases. |
| Storage Temp. | Store at room temperature and away from light |
Properties | |
| Synonym | Gill Hematoxylin Dyeing Solution (Gill ⅱ) |
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