Method of inducing Chinese rose flowering in test tube
A rose and test tube technology, which is applied in the field of inducing rose flowering in test tubes, can solve the problems of no roses, etc., and achieve the effect of high flowering rate, stable technology and good repeatability
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Embodiment 1
[0026] S1. take the stem tip of miniature Chinese rose variety Hula Girl field growth as explant, rinse thoroughly under tap water, then be placed in 5% Tween-20 for 5 minutes, rinse 3-4 times with the distilled water of high temperature and high pressure sterilization, 0.1% mercury chloride (HgCl 2 ) surface sterilized for 4 minutes, rinsed 4-5 times with high temperature and high pressure sterilized distilled water to obtain sterile explants.
[0027] S2. Inoculate the sterile explants into the culture medium to induce callus: MS medium+6-benzylaminoadenine (6-BA) 2mg / L+ naphthalene acetic acid (NAA) 1mg / L+ agar 6g / L+ sucrose 30g / L, to induce callus for 25-30 days.
[0028] S3. The callus is transferred to MS basic medium + 6-benzylaminoadenine (6-BA) 1mg / L + naphthalene acetic acid (NAA) 1mg / L + agar 6g / L + sucrose 30g / L, pH value 5.8, culture 7 -10 days, the callus differentiates into young stems.
[0029] S4. Young stems are inoculated into MS medium+indole butyric ac...
Embodiment 2
[0031] S1. Take the stem tips of the rose variety Kori grown in the field as explants, rinse them thoroughly under tap water, then put them in 5% Tween-20 for 5 minutes, rinse 3-4 times with high temperature and high pressure sterilized distilled water, 0.1% Mercury(HgCl) 2 ) surface sterilized for 4 minutes, rinsed 4-5 times with high temperature and high pressure sterilized distilled water to obtain sterile explants.
[0032] S2. Inoculate the sterile explants into the culture medium to induce callus: MS medium+6-benzylaminoadenine (6-BA) 2mg / L+ naphthalene acetic acid (NAA) 1mg / L+ agar 6g / L+ sucrose 30g / L, to induce callus for 25-30 days.
[0033] S3. The callus is transferred to MS medium+6-benzylaminoadenine (6-BA) 1mg / L+ naphthalene acetic acid (NAA) 1mg / L+agar 6g / L+sucrose 30g / L, pH value 5.8, culture 7-10 day, callus differentiated into young stems.
[0034] S4. Young stems are inoculated into MS medium+indole butyric acid (IBA) 1mg / L+ naphthalene acetic acid (NAA)...
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