未经分离的埃利希腹水肿瘤细胞细胞核中总蛋白和总蛋白- sh含量的定量显微光谱测定。

Microscopica acta Pub Date : 1981-09-01
G Nöhammer, G Khoschsorur
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引用次数: 0

摘要

用宏观和显微光谱法测定了埃利希腹水肿瘤细胞(Ehrlich as腹水tumor cells, EATC)细胞质部分和细胞核的总蛋白和总蛋白- sh含量。通过对Mamaril等人[4]方法的改进,将其分离为细胞质和细胞核两部分。宏观测定总蛋白和总蛋白- sh含量分别采用Lowry等[2]的Folin法和Ellman[1]的DTNB法。总蛋白含量和总蛋白- sh含量的定量微光谱测定分别采用Nöhammer[5]、Nöhammer等[6]的四氮化铵染色法和Nöhammer等[7]的微铬氰(MCN)法。在完整的细胞内,用组织化学方法固定和染色,用显微光谱法测定细胞核总蛋白和总蛋白- sh含量。所谓的“核消去”,即核和核上下部分细胞质的消去之和,被计算为真正的核消去,然后显示出与在孤立核上的微观光谱和宏观测量值的良好对应。真正的核灭绝的计算是基于一种特殊的球形细胞和核的制备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative microspectrometrical determination of the total protein and total protein-SH content of the nuclei of Ehrlich ascites tumor cells without prior isolation.

The total protein and total protein-SH content of both the cytoplasmic fraction and the nuclei of Ehrlich ascites tumor cells (EATC) were determined macroscopically and microspectrometrically. The separation into cytoplasmic and nuclear fraction was performed by a modification of the method of Mamaril et al. [4]. The macroscopical determination of the total protein and the total protein-SH content were performed with the Folin method of Lowry et al. [2] and the DTNB method of Ellman [1], respectively. The quantitative microspectrometrical determinations of total protein content and of total protein-SH content were performed using the tetrazonium staining method of Nöhammer [5] and Nöhammer et al. [6] and the mercurochromcyanide (MCN) method of Nöhammer et al. [7], respectively. Within the intact cells, fixed and stained histochemically, the total protein and the total protein-SH content of the nuclei were determined microspectrometrically. The so called "nuclear extinctions", measured as the sum of the extinctions of the nucleus and of the parts of the cytoplasm above and below the nucleus, were calculated into the true nuclear extinctions, which then show a good correspondence to the values measured both microspectrometrically and macroscopically on isolated nuclei. The calculation for the true nuclear extinctions is based on a special preparation of spherically shaped cells and nuclei.

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