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用活性染料丽华实红紫E-2BL对角蛋白和透明角质颗粒进行染色。

Staining of keratin and keratohyalin with the reactive dye levafix red violet E-2BL.

作者信息

Waldrop F S, Puchtler H, Akamatsu Y

出版信息

Stain Technol. 1976 Jul;51(4):219-25. doi: 10.3109/10520297609116706.

Abstract

Demonstration of keratin in Zenker-fixed skin and in tissues stored in formalin can be difficult because such material is unsuitable for histochemical studies. A reactive dye, Levafix red violet E-2BL, proved useful for demonstration of keratohyalin and some types of keratin. Formalin-, Zenker- and methacarn-fixed sections were pretreated with alkaline alcohol, stained one hour at 60 C in an aqueous solution containing 0.25% Levafix red violet E-2BL plus 0.25% NaCl, rinsed in buffer solution pH 9, dehydrated and mounted. Keratohyalin granules and stratum corneum were colored red violet; hair and tonofibrils remained unstained. In sections prestained with Mayer's acid hemalum, keratohyalin was dark blue. Sulfonated monoazo dyes without reactive groups colored no tissue structures under the conditions of this technic; apparently, Levafix red violet E-2BL is bound via its reactive group. Polarization microscopic studies suggest binding of Levafix red violet E-2BL by an amorphous matrix of keratin. Correlations with chemical data indicate that the staining patterns parallel the distribution of proteins formed in the stratum granulosum.

摘要

在经岑克尔固定的皮肤以及保存在福尔马林中的组织中显示角蛋白可能会很困难,因为这类材料不适合用于组织化学研究。一种活性染料,丽华实红紫E - 2BL,被证明可用于显示透明角质颗粒和某些类型的角蛋白。将经福尔马林、岑克尔和甲醇 - 冰醋酸固定的切片用碱性酒精预处理,在含有0.25%丽华实红紫E - 2BL加0.25%氯化钠的水溶液中于60℃染色1小时,在pH 9的缓冲溶液中冲洗,脱水并封固。透明角质颗粒和角质层被染成红紫色;毛发和张力原纤维未染色。在用迈耶氏酸性苏木精预染色的切片中,透明角质呈深蓝色。在该技术条件下,没有活性基团的磺化单偶氮染料不会使任何组织结构显色;显然,丽华实红紫E - 2BL是通过其活性基团结合的。偏光显微镜研究表明丽华实红紫E - 2BL与角蛋白的无定形基质结合。与化学数据的相关性表明,染色模式与颗粒层中形成的蛋白质分布平行。

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