Cover image of the article: The rapid method of preparing mouse karyotype and mouse chromosomes identified by Gimsa staining and Trypsin-Gimsa banding

Image Credit:J Inflamm Dis

The rapid method of preparing mouse karyotype and mouse chromosomes identified by Gimsa staining and Trypsin-Gimsa banding

Authors

E Mirabzadeh Ardakani,*
*Corresponding Author: Email: emirabzadehardakani@mail.com

Journal of Inflammatory Diseases:Vol. 4, issue 4; 14-22
Published online:Mar 31, 2001
Article type:Research Article
How to Cite:Mirabzadeh Ardakani E. The rapid method of preparing mouse karyotype and mouse chromosomes identified by Gimsa staining and Trypsin-Gimsa banding. J Inflamm Dis. 2024;4(4):e154789. doi:

Abstract

Abstract Background: Preparation and staining of mouse chromosomes by Gimsa and T-G banding is the cornerstone of many researches on diagnosis, prevention and treatment of many diseases, production of new drugs and quality control of biological derivatives. Objective: To provide a sample karyotype of mouse. Methods: Mouse chromosomes were prepared from bone marrow of male outbred mice (NMRI). After culturing and preparing the slides, they were studied by staining with Gimsa and Trypsin-Gimsa (T-G) banding techniques. Karyotypes were prepared according to the standard karyotype of the mouse. Findings: Metaphase with spread from diploid cells contained 40 chromosomes and all of them were characterized by their banding patterns. Conclusion: T-G technique provides greather detail and demonstrates more bands, in contrast with other methods.

Highlights

Copyright

© 2024, Journal of Inflammatory Diseases. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.

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