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本试验对月季实生苗进行了试管快速繁殖和移栽研究。初代培养各种激素试验中，ＭＳ＋ＢＡ２＋ＧＡ１０的培养基较好，本培养基外植体萌发快，增殖高达８～１０倍。４７代培养中产生的细弱苗，转移到壮苗培养基ＭＳ＋ＢＡ０．５＋ＮＡＡ０．５中培养２周，壮苗移植在诱导根原基的ＭＳ＋ＮＡＡ０．５的培养基中培养，经约两周左右培养产生根原基。然后，将它移植于生根培养基上，生根培养基本为１／２ＭＳ＋ＮＡＡ０．５＋３００ｍｇ／ｌ活性碳，强光条件下，温度白大控制在２８℃，夜间控制在２１℃左右。生根后移栽盆土为腐殖士：河砂：锯沫＝１：１：１。盖上烧杯封闭一周后，开始每天提烧杯０．５ｃｍ，３天后，方可移我在花盆中的腐殖土上培养。
In this experiment, rapid growth of test tubes and transplanting of rose seedlings were studied. Primary culture of various hormones in the test, MS + BA2 + GA10 better medium, the medium of explants germination fast, up to 8 to 10 times the proliferation. 47 generations of seedlings generated in culture, transferred to strong seedling medium MS + BA0.5 + NAA0.5 for 2 weeks, strong seedling transplantation rooted in the induction of MS + NAA0.5 medium, after about two weeks of culture to produce root base. Then, it was transplanted on the rooting medium, rooting culture is basically 1 / 2MS + NAA0.5 +300 mg / l activated carbon, under light conditions, the temperature of white control at 28 ℃, night control at about 21 ℃. Rooted after transplanting pots for the humus: river sand: sawdust = 1: 1: 1. Close the beaker for one week, then start a beaker 0.5cm daily, 3 days before I can be moved in the humus soil culture.