Staining of DNA-phosphate groups and DNA-aldehyde molecules with dyes of the azine group.

Microscopica acta Pub Date : 1980-11-01
M K Dutt
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引用次数: 0

Abstract

The investigation reports on the use of safranine-SO2 and phenosafranine-SO2, prepared with N HCl or oxalic acid plus potassium metabisulphite, for staining rat liver sections following Feulgen procedure. It has been found that optimum staining of DNA-aldehyde molecules is possible with safranine-SO2 and phenosafranine-SO2, prepared with N HCl and potassium metabisulphite, upto a duration of one week after the preparation of the dye-reagents. Thereafter, staining intensity of the nuclei produced by the dye-reagents is gradually diminished. Staining of acid-hydrolysed sections is also possible with aqueous solutions of these dyes. Moreover, DNA-phosphate groups can also be stained with aqueous solutions of these dyes after selective extraction of RNA with cold phosphoric acid. The in situ absorption spectra of nuclei, stained for DNA-aldehyde molecules with safranine-SO2, phenosafranine-SO2 and aqueous solutions of these dyes, have been presented in this paper. Also presented herein are absorption data of nuclei stained with these dyes after selective extraction of RNA. It has been found that absorption-peaks of nuclei stained differently are different from one another. The implications of these findings have been discussed.

用氮基染料染色dna -磷酸基团和dna -醛分子。
研究报告了用盐酸或草酸加亚硫酸钾制备的藏红花碱- so2和吩藏红花碱- so2,按Feulgen法对大鼠肝脏切片进行染色。研究发现,用盐酸和亚亚硫酸钾制备的藏红花- so2和吩藏红花- so2,在染料制备后的一周内,对dna -醛分子的染色效果最佳。此后,染色试剂产生的细胞核染色强度逐渐减弱。用这些染料的水溶液也可以对酸水解的切片进行染色。此外,在冷磷酸选择性提取RNA后,这些染料的水溶液也可以染色dna -磷酸基团。本文介绍了用藏红花- so2、吩藏红花- so2及其水溶液染色dna -醛分子的细胞核原位吸收光谱。本文还介绍了选择性提取RNA后用这些染料染色的细胞核的吸收数据。发现染色不同的核的吸收峰是不同的。对这些发现的含义进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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