Production method of paraffin section for observing flower bud differentiation process
A technology of paraffin sectioning and flower bud differentiation, applied in the field of plant sample observation, can solve the problems of incomplete sectioning, high toxicity, and difficult production, and achieve the effects of reducing brittleness, ensuring accuracy, and high accuracy
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Embodiment 1
[0038] Example 1: Microstructure of Hemerocallis shoot tip in vegetative stage
[0039] Take material and fix the air: After dissecting the leaves basally grown on the rhizome of Hemerocallis basalis, take the central point of the stem tip of Hemerocallis basalis and the basal line of the leaves as the axis, and immediately cut carefully 5mm (parallel to the basal line of the leaves) × 3mm ( The central tissue of the Hemerocallis shoot tip (perpendicular to the basal line of the leaf) × 5mm (height), is immersed in a 10ml test tube (with a cover) filled with FPA fixative solution for fixed preservation, and the volume ratio of the material fixative solution is 1:40. Subsequently, put the test tube into a vacuum desiccator, open the test tube cover, and vacuumize for 1-2 hours until all the samples sink to the bottom.
[0040] Dehydration and transparency: After the fixation is completed, pour out the fixative in the test tube and place it on the test tube rack. Sequentially r...
Embodiment 2
[0046] Example 2: Microstructure of Hemerocallis flower buds in flower bud differentiation stage
[0047] In the fixed air extraction stage of obtaining materials in embodiment 1: after dissecting the blades that were basal on the rhizome of Hemerocallis, take the basal line of the central point of the Hemerocallis stem tip and the blade as the axis, and immediately carefully cut 5mm (parallel to the base of the blade) Raw line) × 3mm (perpendicular to the basal line of the leaf) × 5mm (height), the central tissue of the Hemerocallis shoot tip, immersed in a 10ml test tube (with a cover) filled with FPA fixative solution for fixed preservation, the volume ratio of the material fixative solution is 1 :40. Subsequently, put the test tube into a vacuum desiccator, open the test tube cover, and vacuumize for 1-2 hours until all the samples sink to the bottom.
[0048] In the dehydration transparent stage of Example 1: after the fixation is completed, the fixative in the test tube...
Embodiment 3
[0051] Example 3: Microstructure of Hemerocallis flower buds at the stage of small flower bud formation
[0052] In the fixed air extraction stage of obtaining materials in embodiment 1: after dissecting the blades that were basal on the rhizome of Hemerocallis, take the basal line of the central point of the Hemerocallis stem tip and the blade as the axis, and immediately carefully cut 5mm (parallel to the base of the blade) Raw line) × 3mm (perpendicular to the basal line of the leaf) × 5mm (height), the central tissue of the Hemerocallis shoot tip, immersed in a 10ml test tube (with a cover) filled with FPA fixative solution for fixed preservation, the volume ratio of the material fixative solution is 1 :40. Subsequently, put the test tube into a vacuum desiccator, open the test tube cover, and vacuumize for 1-2 hours until all the samples sink to the bottom.
[0053] In the dehydration transparent stage of Example 1: after the fixation is completed, the fixative in the te...
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