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微丝的的英文

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"微丝的"怎么读用"微丝的"造句

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  • fibrillose

例句与用法

  • Synthesis and microwave electromagnetic properties of glass - coated magnetic microwires
    玻璃包覆磁性微丝的制备及微波电磁性能
  • It have been proved that the tip [ ca2 + ] i and the amount of tip f - actin oscillates periodically accompany the oscillatory growth of pollen tubes
    伴随花粉管的振荡生长,花粉管顶端的ca ~ ( 2 + )浓度梯度和微丝的聚合?解聚状态会发生周期性变化。
  • With these transgenic materials , the relationship between tip [ ca2 + ] i and tip - localized f - actin in pollen tubes during the oscillatory growth can be well studied
    该系统的完成为研究花粉管振荡生长过程中ca ~ ( 2 + )与微丝的相互关系做了材料上的准备。
  • Talin is a important f - actin binding protein , two functions of intact talin are the control of actin filament length and the cross - linking of actin polymers . the binding of f - actin to talin significantly increases actin filament stiffness
    Talin是一个重要的f - actin结合蛋白,它可以控制微丝的长度,并且同actin聚合体发生交联, f - actin和talin发生的结合可以显著地增加微丝骨架的强度。
  • Recently , a great number of biochemical analyses and immunoctochemical experiments have proved that actin presents in nuclei and chromosomes in plants and animals , showing that actin is involved in the nuclear processes such as chromosome condensation , rna transcription and so on
    肌动蛋白主要存在于细胞质中,是细胞骨架微丝的重要组成成分,受多种肌动蛋白结合蛋白的调控,参与与细胞形态和结构相关的多种生理过程。
  • Polymer his - tagged peac1 - gfp efficiently activated myosin mg - atpase activity , which indicated that peacl might take part in correlative living activities in vivo . moreover , this result provided experimental proof in vitro for fusing gfp to actin isoform directly to study the dynamics of microfilaments and its regulation in vivo . we prepared rabbit anti - pea actins polyclonal antibodies using peacl as antigen which being expressed and purified from prokaryotic cells , and the antibodies possessed better immunity activity to pea actins
    通过肌动蛋白体外对dnase以及肌球蛋白atpase活性影响的研究,发现单体his - taggedpeac1 - gfp能显著抑制dnase活性,在肌动蛋白聚合条件下能有效激活肌球蛋白atpase活性,这一结果预示着peac1在体内可能参与相关的生命活动,为利用gfp直接与肌动蛋白异型体融合来研究体内微丝的动态变化及其调节提供了实验依据。
  • In this study , in order to examine the dynamics of tip [ ca2 + ] i together with the dynamics of tip - localized f - actin in vivo , a kind of double labeled material was constructed . the ca2 + and actin microfilaments of arabidopsis pollen tubes were labeled by cameleon and gfp - mtalin respectively
    本研究以拟南芥花粉管为材料,通过转基因技术,将分别标记ca ~ ( 2 + )和微丝的两种荧光蛋白cameleon与gfp - mtalin在花粉管中同时表达,实现活体花粉管中ca ~ ( 2 + )与微丝的同时标记。
  • The fusion gene ofgfp : mtn ( mtn is binding domain of microfilament binding protein talin , which can show the microfilament in living cell ) was transferred to arabidopsis thaliana . stable expression of gfp - mtn can visualize the actin cytoskeleton in different types in living cells without affecting cell morphology and function
    将gfp : mtn ( mtn是微丝结合蛋白talin的微丝结合域,可以显示活体细胞中微丝的结构)导入拟南芥后,发现表达的融合蛋白能够标记微丝骨架,同时又不影响植物细胞的正常形态和功能。
  • The his - tagged peacl - gfp purified from the supernatants could polymerize into green fluorescent filamentous structures with diameter , length and shape being identical to that of muscle f - actins , which could be labeled by tritc - phalloidin ( a specific agent for staining actin microfilaments ) , and were identified as having a 9 nm diameter by negative staining , corresponding with that of the muscle f - actins ( 7 - 10 nm ) . under polymerization conditions , his - tagged peacl - gfp polymerized with kinetics similar to those of skeleton muscle actin , that is , an obvious lag nucleation period at the beginning of polymerization and an s - like typical polymerization curve could be obtained . the critical concentration is 0 . 75 umol / l near to that of chicken muscle actin ( 0 . 56 umol / l ) under the same condition
    荧光标记结合荧光显微观察表明:从可溶性上清中纯化的his - taggedpeac1 - gfp聚合形成的微丝不仅可以直接在荧光显微镜下观察,也可被微丝的特异标记物鬼笔环肽所标记,而且其直径、长度以及形态上与已知的聚合肌动蛋白荧光丝一致;电镜负染的结果进一步证实其直径为9nm ,与传统微丝直径相当( 7 ? 10nm ) ;聚合曲线有明显的停滞期,为典型的s型聚合曲线,聚合临界浓度为0 . 75 mol l ,这一结果与已有报道相似。
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