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zygotes相关的网络例句

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与 zygotes 相关的网络例句 [注:此内容来源于网络,仅供参考]

Lower concentration of the microinjected DNA, choosing CZB and zygotes with good quality can enhance efficiency of microinjection.

选用较低的基因浓度,良好的操作介质CZB,使用质量好的受精卵,会提高显微注射的效率。

AIM: To establish a transgenic mouse model of Hi1tchirtson-Gilford progeria syndrome and observe the effect of mutant lamin A on the implantation and survival ability of injected mouse zygotes.

目的:制备Hutchinson-Gilford早老症转基因小鼠模型,观察突变的核纤层蛋白A对小鼠受精卵着床和成活情况的影响。

To make the transgenic mice: We purified the gene fraction nestin-hsp68-EGFP and injected it into pronucleus of mouse zygotes to generate the transgenic mice.

1。转基因小鼠的获得:纯化基因片段nestin-hsp68-EGFP,用显微注射方法把基因片段注射到受精卵的雄原核中,获取转基因小鼠。

Then the linear vector was microinjected into the pronucleus of the KM×B6D2F1 zygotes to produce the transgenic mice. Thirty-four adult mice were produced from 286 of injected embryos.

用显微注射方法,将线性化的载体DNA注入KM ×B6D2F1小鼠受精卵的的原核内部,然后将胚胎移植到输卵管内,13只受体怀孕产仔。

Methods: the hbv transgenic mice were generated by microinjection of 1.3 copies hbv genome into the pronucleus of fvb/n zygotes. the pcr assay,elisa,rt-pcr and immunohistochemical methods were used to detect the hbv integration,replication and expression in the transgenic mice.

采用受精卵显微注射法,制备hbv转基因小鼠,用pcr,elisa,荧光定量pcr和免疫组化的方法研究hbv基因在转基因小鼠体内的整合、复制和表达情况。

Lamin A gene cDNA lacking of 150 basyls at the end of the eleventh extron was cloned into pcDNA3.1 carrier, and the recombinant plasmid pcDNA3.1-mutant LMNA cDNA was injected into the male pronucleus of mouse zygotes, then the zytotes was replanted into the oviducts of pseudopregnant mice.

实验方法:将缺失了第11外显子末端150个碱基的LMNA基因cDNA克隆到pcDNA3.1载体,应用原核显微注射方法将线性化的pcDNA3.1-mutant LMNA注射到小鼠受精卵的雄原核,再将注射后的受精卵移植至假孕鼠的输卵管。

A thick - walled structure in which sporozoan zygotes develop and that serves to transfer them to new hosts.

孢子一种外壁很厚的组织,孢子在这里受精发育,再把他们转入新的个体中

Long-distance PCR was used to amplify the β-actin gene for black carp based on the β-actin gene sequences of Cyprinidae. Construct of EGFP expression system containing 5'UTR of β-actin gene for black carp was transferred into zygotes of mud loach and COS-7 cells and the results showed that 5'UTR of β-actin gene for black carp could be used as the promoter of the"all-fish"transgene.

基于鲤科鱼类Beta-肌动蛋白基因序列,采用长片段PCR技术,克隆了青鱼β-actin基因DNA片段,并构建了青鱼β-actin基因5'启动调控区绿色荧光蛋白表达载体,通过显微注射泥鳅胚胎和COS-7细胞转染实验,证明了所克隆的青鱼β-actin基因5'启动调控区具有启动调控功能,并用之来构建&全鱼&基因的启动子部分。

The mature egg cell was an inactive cell with only a few polysomes. At the early zygote stage, a large number of ribosomal precursors were produced by the nucleolus, and many polysomes appeared in the cytoplasm, which suggests a high level of metabolism. Zygote at the dormancy stage had a small nucleolus and marked decrease in ribosomes, as shown by a few polysomes, which suggests decreased metabolism. Zygotes in the prophase of mitosis and two-celled proembryo became active again in metabolism, for a prominent nucleolus, high density of ribosomes and increased number of polysomes in the cytoplasm.

结果如下:在成熟卵细胞中多聚核糖体数量不多,且细胞代谢活性较弱;初期合子内,核仁大量合成核糖体前体物质,胞质中多聚核糖体数目众多,细胞代谢活性较强;休眠期合子的核仁变小,胞质中核糖体数量急剧减少,仅有少量多聚核糖体,细胞代谢活性较弱;合子分裂前期和二细胞原胚期,核仁显著,胞质中核糖体的密度增加,出现大量多聚核糖体,细胞代谢活性较强。

Finally, transfer 8-16 zygotes into oviduct of pseudopregnant female recipients mice.

最后,将注射后的受精卵植入代理孕母鼠输卵管中。

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