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芽诱导     
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  bud induction
     The results showed explants of differentiation rate attained to 77.3% with medium MS+6-BA 3.0mg/L+NAA 0.1mg/L in bud induction;
     探索了米邦塔食用仙人掌组培快繁技术,得出不定芽诱导使用培养基MS+6-BA 3.0mg/L+NAA 0.1mg/L,外植体分化率达77.3%;
短句来源
     the adventitious bud induction culture medium makes of MS + 6-BA 2.0 mg/L + NAA0.2mg/L;
     不定芽诱导培养基为MS+6-BA 2.0mg/L+NAA0.2mg/L;
短句来源
     The best media for different cultural stages are bud induction MS+6-BA 2 mg/L+NAA 0.2 mg/L, Differentiation bud MS+6-BA 1 mg/L+NAA 0.1 mg/L, Strengthening seedling MS+0.1 mg/L NAA, Rooting 1/2MS+IBA 0.2 mg/L.
     各培养阶段的最适培养基分别为,芽诱导培养基MS+2mg/L6-BA+0.2mg/LNAA,芽分化培养基MS+1mg/L6-BA+0.1mg/LNAA,壮苗培养基MS+0.1mg/LNAA,生根培养基1/2MS+0.2mg/LIBA.
短句来源
     The results showed that the appropriate medium for bud induction is MB+6-BA 1.0 mg/L+NAA 0.2 mg/L, the medium of multiplication is (MB+)6-BA 0.5 mg/L+NAA 0.1 mg/L, and the medium of rooting is 1/2 MS+NAA 0.3 mg/L.
     结果表明:适于"米邦塔"食用仙人掌芽诱导分化的培养基为MB+6 BA1.0mg L+NAA0.2mg L,继代增殖的培养基为MB+6 BA0.5mg L+NAA0.1mg L,生根培养基为1 2MS+NAA0.3mg L;
短句来源
     This paper studied the rapid propagation method of Opuntia vilpa alta Haw in plant tissue culture,We got the results: explants of differentiation rate to 77.3% with medium MS 6-BA 3.0mg/L&NAA 0.1 mg/L in bud induction;
     探索了米邦塔食用仙人掌组培快繁技术,得出不定芽诱导使用培养基MS+6-BA 3.0mg/L+NAA 0.1mg/L,外植体分化率达77.3%;
短句来源
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  shoot induction
     (2) 65.83% shoot induction on MS medium supplemented with 0.1 mg·L-1 IAA, 0.5 mg·L-1 ZT, 30 g·L-1 sucrose and 8 g·L-1 agar;
     (2)不定芽诱导最适培养基为MS+IAA 0.1 mg·L-1+ZT 0.5 mg·L-1+sucrose 30 g·L-1+agar 8 g·L-1,不定芽诱导率为65.83%;
短句来源
     (2)shoot induction:MS+ 6 BA 0.5mg/L+NAA 0.5mg/L;
     (2 )芽诱导 ,MS +6 BA 0 .5mg/L +NAA 0 .5mg/L ;
短句来源
     As for shoot induction, MS+0.5 mg/L BA+0.1 mg/L NAA was the best combination in this experiment.
     适宜的芽诱导培养基为MS+0.5mg/L BA+NAA 0.1mg/L。
短句来源
     The optimum m ed ium wasMS5(MS+6-BA 1.5 mg /L+NAA 0.1 mg /L) for shoot induction,MS3(MS+6-BA 1.5 mg /L+NAA 0.2 mg /L) for subcu lture and MS10(MS+NAA 0.3 mg /L+ IBA 0.5 mg /L) for rooting.
     ,并以其芽条为外殖体,在10种MS培养基上添加不同浓度NAA,6-BA和IBA进行了芽诱导、增殖和生根培养研究,以加速在云南产业化种植基地建设。 结果表明,其效果甚为理想:MS 5培养基(MS+6-BA 1.5 mg/L+NAA 0.1 mg/L)适宜芽的诱导分化;
短句来源
     The optimum medium of shoot induction was 1/2MS+KT1.0 mg/L+NAA0.05 mg/L with induction rate of 83.3%, and induction time of 76 days.
     芽诱导以1/2MS+KT1.0 mg/L+NAA0.05 mg/L为最优。 芽诱导率达到83.3%,诱导时间为76天。
短句来源
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  shoot induce
     the worst shoot induce status was shanyou 31, this specie's shoot induce rate only was 9.5% on shoot induce medium 2.
     芽诱导率以汕油523最高,在芽诱导培养基1中为93.1%,汕油31最差,在芽诱导培养基2中仅为9.5%。
短句来源
  bud inducement
     NAA and 6-BA were necessary in this study. The frequency of chimera bud inducement reached 6.33% when incised part was treated with 2.0 mg/L 6-BA +1.0 mg/L NAA.
     6-BA和NAA为该体系合成榨菜和甘蓝嵌合体所必需,嫁接伤口以2mg/L 6-BA+1mg/L NAA处理时,榨菜和甘蓝嵌合体芽诱导效率达6.33%。
短句来源
     The results showed that the best medium for adventitious bud inducement is MS adding with(3.56) mg/L 6-BA and 0.294 mg/L NAA for a nearly 100% induction rate.
     试验结果表明,成熟胚不定芽诱导以MS培养基最佳,附加0.294 mg/L的NAA和3.56 mg/L的6-BA时,诱导率接近100%;
短句来源
     A Study on Breeding Autotetraploid Rices by the Bud Inducement
     种芽诱导获得同源四倍体水稻技术的研究
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  bud induction
The frequency of flower bud induction in general increased with increasing concentrations of cytokinins, the optimal levels being 3 mg/l of KN or 4 mg/l of BAP.
      
A sequential treatment of callus with increasing BA levels and decreasing NAA ensured shoot bud induction.
      
Embryos remained on bud induction medium for 21 days and then were transferred to the same basal medium without 6-benzylaminopurine to promote bud development and subsequent shoot elongation.
      
The optimum cytokinin (BA) concentration for bud induction was 2 μM BA.
      
Embryos placed on bud induction medium produced approximately 20 adventitious buds per embryo under control conditions.
      
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  shoot induction
Immature leaflet explants were found to be more responsive to shoot induction than mature leaflet explants.
      
Co-segregation of the NR- phenotype and the altered response to shoot induction on standard medium suggest the involvement of the nitrate-assimilatory pathway in determining shoot regeneration ability.
      
minima, shoot induction was obtained only after transformation by bacteria carrying pGV 2215.
      
In response to shoot induction, about 10% of the root lines produced shoots through callus formation.
      
Incubation in semi-solid media at 15°C with continuous illumination followed by growth in agitated liquid media was essential for shoot induction and development in primary explants of E.
      
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