Method for establishing eremochloa ophiuroides highly efficient regeneration system with young spike as explant
A high-efficiency regeneration and explant technology, applied in the field of plant biotechnology research, can solve the problem that it is not suitable for large-scale screening of somatic mutants in micropropagation, high-efficiency genetic transformation, long callus induction period, and callus tissue. Poor differentiation ability and other problems, to achieve the effect of improving callus induction rate, easy implementation and induction efficiency
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[0038] (1) Experimental materials
[0039] Take the fresh and tender young spikes (inflorescences) that have not drawn out the leaf sheaths at the beginning of flowering stage of E092-1 as the explant material (such as figure 1 shown);
[0040] (2) Medium
[0041] The basic medium was MS medium composed of macroelements, trace elements and vitamins, supplemented with 30.0 g / L sucrose (Sigma) and 8.0 g / L agar (Japan);
[0042] Callus induction medium MS1: add 2.0 mg / L of 2,4-D (Sigma D-7299) or 4.0 mg / L of 2,4-D (Sigma D-7299) or 6.0 mg / L of 2,4-D (Sigma D-7299), 0.1 mg / L of BAP (Sigma B3408);
[0043] Subculture medium MS2: Add 1.5 mg / L 2,4-D (Sigma D-7299) and 0.1 mg / L BAP (Sigma B3408) to the basic medium;
[0044] Green shoot differentiation medium MS3: Add 2.0 mg / L of KT (Sigma K-3378), 0.1 mg / L of NAA (Sigma N0640), or 2.0 mg / L of BAP (Sigma B3408), 0.1 mg / L of NAA (Sigma N0640), or 2.0 mg / L of CPPU (Sigma C2791), 0.1 mg / L of NAA (Sigma N0640);
[0045] Test tube see...
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