计算溶液所需的质量、体积或浓度。
盐酸乙醇快速分化液
有货
为什么选择此级别
BioReagent,生物染色剂,用于显微镜 级 ，适用于对基线干扰要求严格的色谱和分析工作流程。
储存与运输
室温。常规运输 。请查阅批次 COA 获取详细规格。
质量文档
SDS、COA、产品数据表及规格说明书均可下载。可通过批号查询获取批次 COA。
文献证明
在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。
概述
分化作用是指组织染色后用某些特定的溶液将组织过多结合的染色剂脱去，这个过程称为分化作用，所用的溶液称为分化液。在HE染色和其他染色中常用1%盐酸乙醇作为分化液，因酸能破坏苏木素的醌型结构，使组织与色素分离而退色，再进行伊红染色，才能保证细胞核与细胞浆染色的分明。
盐酸乙醇分化液主要由盐酸、乙醇、去离子水等组成，经常用于苏木素染色、苏木素伊红染色 (HE染色)或Masson染色等涉及苏木素染色时，可缓慢地降低细胞浆等背景性的苏木素染色并使细胞核苏木素染色更清晰的溶液，是一种非常重要的辅助试剂。使用本产品可获得更好的苏木素染色效果。本产品的基本原理是在酸性条件下，可以有效洗去细胞核以外的苏木素染色，从而降低背景；同时，也可以使细胞核着色过深的区域染色适当减弱，使染色更清晰。
盐酸乙醇快速分化液分化时间比较短，一般需要5~15秒左右。如果希望更快速地分化，可以考虑选购盐酸乙醇超快速分化液，或用1%酸性乙醇分化液。该试剂仅用于科研领域，不适用于临床诊断或其他用途。
自备材料：
1、自来水或蒸馏水、4%多聚甲醛或中性福尔马林固定液、二甲苯或浸蜡脱蜡透明液
2、系列乙醇、苏木素染色液、伊红染色液、蓝化液 (稀氨水、碳酸锂溶液等）、中性树胶
操作步骤 (HE染色步骤，仅供参考)：
1、组织脱蜡至水。
2、苏木素染色液染色3-8min。
3、自来水或蒸馏水冲洗5-10s。
4、盐酸乙醇快速分化液分化5-15s。
5、自来水冲洗20-30s。
6、蓝化液返蓝20-40s或温水返蓝10min。
7、80%乙醇脱水30-60s。
8、伊红染色液 (醇溶)染色20-60s。
9、梯度乙醇脱水，二甲苯或环保脱蜡透明液透明，中性树胶封片，镜检。
注意事项：
1、不同样品和不同染色要求，所需要的分化时间会有所不同。初次使用本产品建议先摸索不同分化时间，根据镜下观察结果，确定最优的分化时间。
2、染色后的分化为选做步骤，但分化后核质染色更清晰，核膜及染色质的形态结构更清楚。
3、本产品易挥发，请注意密闭保存。为避免挥发导致的使用效果下降，开启后宜尽快用完。
4、本产品有腐蚀性，操作时请小心，并注意有效防护以避免直接接触人体或腐蚀其他物品。
5、为了您的安全和健康，请穿实验服并戴一次性手套操作。
6、试剂开封后请尽快使用，以防影响后续实验效果。
Differentiation refers to the process of removing excess stain bound to tissues using specific solutions after tissue staining. The solution used in this process is called a differentiation solution. In HE staining and other staining methods, 1% hydrochloric acid-ethanol is commonly used as a differentiation solution. Acids can disrupt the quinone structure of hematoxylin, separating tissues from the pigment and causing discoloration. Subsequent eosin staining ensures clear differentiation between cell nuclei and cytoplasm.
Hydrochloric acid-ethanol differentiation solution mainly consists of hydrochloric acid, ethanol, and deionized water. It is frequently used in hematoxylin staining, hematoxylin-eosin staining (HE staining), Masson staining, and other procedures involving hematoxylin. As a crucial auxiliary reagent, it can slowly reduce background hematoxylin staining in structures like cytoplasm while enhancing the clarity of hematoxylin staining in cell nuclei. Using this product ensures better hematoxylin staining results. Its basic principle is that under acidic conditions, it can effectively remove hematoxylin staining outside cell nuclei to reduce background. Meanwhile, it can appropriately lighten over-stained areas of cell nuclei, resulting in clearer staining.
The differentiation time of Rapid Hydrochloric Acid-Ethanol Differentiation Solution is relatively short, generally about 5 to 15 seconds. If faster differentiation is required, Ultra-Rapid Hydrochloric Acid-Ethanol Differentiation Solution or 1% Acidic Ethanol Differentiation Solution can be selected. This reagent is for research use only and not intended for clinical diagnosis or other applications.
Materials to Be Prepared by the User
1. Tap water or distilled water, 4% paraformaldehyde or neutral formalin fixative, xylene or wax-immersion dewaxing and clearing solution
2. A series of ethanol solutions, hematoxylin staining solution, eosin staining solution, bluing solution (e.g., dilute ammonia water, lithium carbonate solution), and neutral balsam
Operating Procedures (HE Staining Steps, for Reference Only)
1. Dewax the tissue to water.
2. Stain with hematoxylin staining solution for 3-8 minutes.
3. Rinse with tap water or distilled water for 5-10 seconds.
4. Differentiate with Hydrochloric Acid-Ethanol Fast Differentiation Solution for 5-15 seconds.
5. Rinse with tap water for 20-30 seconds.
6. Blue the tissue with bluing solution for 20-40 seconds or with warm water for 10 minutes.
7. Dehydrate with 80% ethanol for 30-60 seconds.
8. Stain with alcoholic eosin staining solution for 20-60 seconds.
9. Dehydrate with gradient ethanol solutions, clear with xylene or environment-friendly dewaxing and clearing solution, mount the slide with neutral balsam, and examine under a microscope.
Precautions
1. The required differentiation time varies depending on different samples and staining requirements. For first-time use, it is recommended to test different differentiation times and determine the optimal duration based on microscopic observations.
2. Post-staining differentiation is an optional step, but it improves the clarity of nucleus-cytoplasm staining and enhances the visibility of nuclear membranes and chromatin morphology.
3. This product is volatile; store it in a sealed container. To avoid reduced effectiveness due to volatilization, use it as soon as possible after opening.
4. This product is corrosive. Operate with caution and take effective protective measures to avoid direct contact with the human body or corrosion of other items.
5. For your safety and health, wear a lab coat and disposable gloves during operation.
6. Use the reagent as soon as possible after opening to prevent adverse effects on subsequent experimental results.
规格
别名
盐酸酒精快速分化液 | 苏木素快速分化液 | HE 染色快速分化液 | 快速脱色分化液
英文别名
Acid Alcohol Fast Differentiation Solution
规格或纯度
BioReagent, 生物染色剂, 用于显微镜, 1×
稳定性与储存
Store at room temperature long term (24 months).
英文名称
Hydrochloric Acid-Ethanol Fast Differentiation Solution
储存条件
室温
运输条件
常规运输
名称和识别符
分子类型
生物试剂/缓冲液
技术文档
高级数据
质检证书（CoA,COO,BSE/TSE 和分析图谱)
C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:
通过匹配包装上的批号来查找并下载产品的 COA，每批产品都进行了严格的验证，您可放心使用！
| 批号(Lot Number) | 证书类型 | 货号 |
|---|---|---|
 ZJ26F0838169 |
分析证书 | A743394 |
| ZJ26F0838168 |
分析证书 | A743394 |
技术文档和文章
Applications and Comparison of Histological Counterstaining, Collagen Evaluation, and Protein Staining Methods
目录： 技术文章
生物染色剂
目录： 阿拉丁试剂的规格、级别和纯度
Principles and methods of smear staining, microbiological staining, and fundamental dye systems
目录： 技术文章
Masson’s Trichrome Stain (Masson’s Trichrome) Standard Operating Procedure (SOP)
目录： 实验方案（Protocols）
溶液计算器
选择需要帮助选择级别？
我们的级别选择指南涵盖了目录中所有的变体的纯度、稳定剂状态和应用适用性。
查看 BioReagent 级别指南 → 查看 Biological Stain 级别指南 → 查看 for Microscopy 级别指南 →产品仅提供给经过验证的企业、机构和合格的专业人员用于研发。不适用于人类、动物、诊断或治疗。
Copyright © 2023至今 上海阿拉丁生化科技股份有限公司 保留所有权利。
危险品化学品经营许可证（带存储）