Vitrification ultralow-temperature preserving method for agapanthus embryogenic callus
A technology of embryogenic callus and vitrification ultra-low temperature, applied in gardening methods, plant preservation, botanical equipment and methods, etc., can solve the problems of low survival rate, failure to survive, and difficulty in preserving plant materials
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[0037] 1. Experimental materials
[0038] 1.1 Experimental object: Agapanthus embryogenic callus was propagated in MS solid medium containing 1.5 mg / L picloram for 20 days at 25°C, and the obtained friable and loose embryogenic callus was used as a vitrification cryopreservation experiment Object (for the preparation method, please refer to the literature "Research on Rapid Propagation Technology of Blue Lily", Fan Xianli, 2009, Master's Degree Thesis of Shanghai Jiaotong University).
[0039] 1.2 Experimental reagents
[0040] 1.2.1 The loading solution contains 2M glycerol, 0.4M sucrose, 10mM KNO 3 MS culture medium.
[0041] 1.2.2 Vitrification solution is MS culture solution containing 30wt% glycerol, 15wt% ethylene glycol, 15wt% dimethyl sulfoxide, and 0.4M sucrose.
[0042] 1.2.3 The washing solution contains 1.2M sucrose and 10mM KNO 3 MS culture medium.
[0043] 1.2.4 The pretreatment medium is MS solid medium with sucrose content of 0.3M, 0.5M and 0.7M respective...
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