Feulgen stain - определение. Что такое Feulgen stain
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Что (кто) такое Feulgen stain - определение

Feulgen; Feulgen reaction

Robert Feulgen         
GERMAN CHEMIST
Robert Joachim Feulgen; Feulgen, Robert
Joachim Wilhelm Robert Feulgen (2 September 1884 – 24 October 1955) was a German physician and chemist who, in 1914, developed a method for staining DNA (now known as the Feulgen stain) and who also discovered plant and animal nuclear DNA ("thymonucleic acid") congeniality.
May–Grünwald stain         
  • May Grünwald–Giemsa staining of bone marrow cells taken from a patient with [[hereditary folate malabsorption]], from a case report by Yukari Sakurai et al., 2022<ref name="Sakurai2022">Sakurai, Y., Toriumi, N., Sarashina, T. et al. An infantile case of hereditary folate malabsorption with sudden development of pulmonary hemorrhage: a case report. J Med Case Reports 16, 268 (2022). https://doi.org/10.1186/s13256-022-03448-x</ref>
May–Grünwald stain or May–Grünwald–Giemsa stain is used for the staining of slides obtained by fine-needle aspiration in a histopathology lab for the diagnosis of tumorous cells.
Jaswant Singh–Bhattacharji stain         
A RAPID STAINING METHOD FOR DETECTION OF MALARIA.
Jaswant–Singh–Bhattacharji (JSB) stain; Jaswant-Singh-Bhattacherji (JSB) stain; Jaswant Singh-Bhattacherji (JSB) stain; Jaswant–Singh–Bhattacherji (JSB) stain; Jaswant Singh–Bhattacherji (JSB) stain; JSB stain; Jaswant Singh Bhattacharji stain; Jaswant-Singh-Bhattacharji (JSB) stain; Jaswant Singh-Bhattacharji (JSB) stain; Jaswant Singh–Bhattacharji (JSB) stain; Jaswant Singh-Bhattacharji stain
Jaswant Singh–Bhattacharji stain, commonly referred to as JSB stain, is a rapid staining method for detection of malaria. It is useful for the diagnosis of malaria in thick smear samples of blood.

Википедия

Feulgen stain

Feulgen stain is a staining technique discovered by Robert Feulgen and used in histology to identify chromosomal material or DNA in cell specimens. It is darkly stained. It depends on acid hydrolysis of DNA, therefore fixating agents using strong acids should be avoided.

The specimen is subjected to warm (60 °C) hydrochloric acid, then to Schiff reagent. In the past, a sulfite rinse followed, but this is now considered unnecessary. Optionally, the sample can be counterstained with Light Green SF yellowish. Finally, it is dehydrated with ethanol, cleared with xylene, and mounted in a resinous medium.

DNA should be stained red. The background, if counterstained, is green.

The Feulgen reaction is a semi-quantitative technique. If the only aldehydes remaining in the cell are those produced from the hydrolysis of DNA, then the technique is quantitative for DNA. It is possible to use an instrument known as a microdensitometer or microspectrophotometer to actually measure the intensity of the pink Feulgen reaction for a given organelle. Using this procedure, it was early determined that interphase cells were composed of two populations, those with diploid DNA and those with tetraploid DNA (two complete genomes). The nuclei looked identical, but one contained twice as much DNA. This gave rise to the division of the interphase period of the cell cycle to G1, S, and G2 phases based on the synthesis of that extra DNA.