Viability detection technology for acacia rachii pollen culture in vitro
A technology for in vitro culture and viability detection of pollen, applied in horticulture, botanical equipment and methods, horticultural tools/equipment, etc. Restrict the yield and quality of seed gardens, and achieve the effect of low natural pod setting rate, simple method, and high pollen sowing.
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Embodiment 1
[0032] During the blooming season of Acacia mazhan in late September, collect fresh flower branches containing many spikes that have not been interviewed by insects before 7 o'clock, put them in a small bucket with clear water, and bring them back to the laboratory for standby; use 20% Sucrose + 150mg / L boric acid + 0.25mmol / L calcium nitrate concentration to make a liquid medium, drop 3 drops in the groove of the concave glass slide, take the 2 segments of inflorescences that have been collected and cut into multiple segments, and clamp them in the medium with tweezers Rinse for 1 circle without covering the cover glass, then put the concave glass slide flat into a culture dish lined with wet filter paper, and keep the culture humidity at 26°C and the humidity at 85%. After culturing for 1.5, 4.0, 6.0, and 8 hours, put them under an optical microscope and observe the number of pollen germinations by conventional methods. The optical microscope pictures are respectively figur...
Embodiment 2
[0034] During the flowering season of the red bean acacia in mid-May, collect fresh flower branches containing many spikes that have not been interviewed by insects before 7 o'clock, put them in a small bucket with clear water, and bring them back to the laboratory for standby; use 15% sucrose + 100mg / L boric acid + 0.5mmol / L calcium nitrate to make a liquid medium, drop 2 drops in the groove of the concave glass slide, pick fresh inflorescences and cut them into multiple sections, pick up 3 sections with tweezers and rinse in the medium for 1 circle , do not cover with a cover glass, and then put the concave glass slide flat into a petri dish lined with wet filter paper, keep the culture humidity at 28°C, and the humidity at 88%, after culturing for 8 hours, place it under an optical microscope and observe it by conventional methods Germinated amount of pollen.
Embodiment 3
[0036] During the blooming season of the large-leaved straight-stalked acacia in early October, collect fresh flower branches containing many spikes that have not been interviewed by insects before 7 o'clock, put them in a small bucket with clear water, and bring them back to the laboratory for subsequent use; 18% sucrose + 130mg / L boric acid + 0.35mmol / L calcium nitrate concentration to make a liquid medium, drop 2 drops in the groove of the concave glass slide, take the 3 segments of inflorescences that have been collected and cut into multiple segments, clamp them with tweezers and culture them Rinse in the base for 1 circle, without covering the cover glass, then put the concave glass slide flat into a culture dish lined with wet filter paper, keep the culture humidity at 27°C, and the humidity at 90%, after culturing for 8 hours, place it under an optical microscope Next, the number of pollen germination was observed by conventional methods.
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