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愈伤组织分化的英文

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"愈伤组织分化"怎么读用"愈伤组织分化"造句

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  • callus differentiation

例句与用法

  • Fig 2 . differentiation of young shoots from transformed callus
    图2 :从基因枪轰击过的愈伤组织分化出大量的小苗。
  • The relationship between the differentiation of rice callus and the proportion of different plant hormones
    水稻愈伤组织分化与不同激素配比关系的研究
  • 2 . according to the effect of combination of different hormone concentration in the medium on callus formation and shoot induction of tomato cotvledons , we defined mso + 2 . 0mg / l ba + - 0 . 2mg / l iaa as optimum differential medium
    根据番茄子叶外植体在加有不同激素浓度配比的培养基上愈伤组织分化和芽再生的情况,确定最佳分化培养基为ms _ 0 + 2 . 0mg / lba + 0 . 2mg / liaa ; 3
  • Bap performed more important function than kt in differentiation of tall fescue embryogenic calli , but better results could be achieved with combination of 2mg / l bap and 0 . 5mg / l kt . at this cytokinin level , 0 . 5mg / l naa was recommended to obtain the highest callus regeneration frequency . plant regeneration could be evidently boosted when embryogenic calli were pre - differentiated on high - osmoticum medium with 60g / l sucrose , and / or when the pre - differentiated compact calli were differentiated on differentiation medium solidified with l0g / l agar
    高羊茅胚性愈伤组织分化时, bap的作用要比kt大,但2mg lbap与0 . 5mg lkt配合可获得更佳的效果;在该细胞分裂素水平下,生长素naa用0 . 5mg l ,愈伤组织再生率最高;胚性愈伤组织先在含60g l蔗糖的分化培养基上高渗预分化,以及经高渗预分化后的致密愈伤组织在琼脂浓度为10g l的分化培养基上分化,能明显促进愈伤组织的植株再生;在分化培养基中添加脯氨酸导致愈伤组织再生率下降,但同时有减少白化苗再生的趋势。
  • An in vitro plantlet regeneration system was established from rhizome lumps in polygonatum cyrtonema hua and mannose - binding lectin in cultured rhizome was determined by sds - page and hemagglutination assays and also analysised by rt - pcr and comparison of the nueleotide sequences and amino acid deduced with natural polygonatum cyrtonema hua lectin ii .
    利用野生囊丝黄精的幼嫩根状茎作外植体,诱导形成愈伤组织,愈伤组织分化出不定芽,进而产生试管苗,试管苗经移栽试验,成活率为75 ,其外观性状与野生植株无明显差异。
  • Pre - differentiation and proper partial desiccation of calli before transferred to regeneration medium was found to apparently improve the frequency and quality of plant differentiation . with our optimized culture condition and treatment style , induction frequency of pei ' ai64s and 9311 can be reached 62 . 45 % and 85 . 30 % respectively and after 3 months of subculture calli can remain high - quality embryogenic state , when high - quality embryogenic calli after two times of subculture were used as acceptor , callus differentiation frequency can arrive at 85 . 5 % and 87 . 7 % respectively
    采用我们优化后的培养条件与处理方式,培矮64s和9311愈伤组织的诱导频率分别可达到62 . 45和85 . 30 ;继代培养时间达三个月左右仍能保持较好的胚性生长状态;对于继代两次胚性生长状态良好的愈伤组织分化频率分别可达到85 . 5和87 . 7 。
  • Signals were strong in the cell periphery of procambium , and longitudinal signals were stronger than lateral ones ; in root ground meristem cytoplasm , concentration in the perinuclear region was stronger than one in the cell periphery . in cell periphery of root ground meristem , distribution of actin mrna was heterogeneous , longitudinal signals were stronger than lateral ones ; in callus meristem cytoplasm , concentration in the perinuclear region was low ;
    这表明,从棉花愈伤组织薄壁细胞到鸟巢状管胞团再到正常苗的过程中肌动蛋白mrna的分布和浓度都有明显的变化,而在这里愈伤组织在分化到鸟巢状管胞团后就不再继续发育,因而推测,肌动蛋白mrna分布和浓度可能影响愈伤组织分化出正常的植株。
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