A method for 3D fluorescence in situ hybridization of poplar root tips based on frozen sections
A technique of fluorescence in situ hybridization and frozen section, which is applied in the field of molecular cytogenetics, can solve the problems of staying, unable to visually display the real space occupancy of chromosomes, and unable to distinguish the real space occupancy of chromosomes in cells, etc.
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[0038] 1. Root apex fixation and cleaning
[0039] The young root tips of poplar trees with a length of about 5 mm were intercepted and immediately immersed in Carnot's fixative (3:1 volume ratio of absolute ethanol and glacial acetic acid) for more than 1 h.
[0040] The fixed root tips were washed twice with pure water for 10 min each time to remove Carnot's fixative.
[0041] 2. Embedding, sectioning and washing
[0042] The cleaned root tip was placed on a glass slide, and then the apical tissue with a length of about 2-3 mm was cut off with a double-sided blade, and the excess water on the surface was absorbed with filter paper. The tissue was embedded on the sample head in a cryostat (Leica, CM3050 S) with a special tissue embedding medium (Tissue Freezing Medium, Leica), and the embedded sample was frozen in a cryosection box for 30 min at a temperature of -20 ℃, the temperature of the sample head during sectioning is -16℃, the thickness of the section is 8µm, and the...
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