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GV oocytes with normal shape were not obtained in the group which was stored at 20℃ for 24 h and at 25℃ for 14 h; A blastula rates (64%) of all groups in average was gotten in culturing 2-cell in vitro, and there is no significant difference in temperature and time of storage. After transplantating some of the 2-cell embryos which were obtained from GV oocytes stored at 15'C for 8 h, normal infant mice could be obtained.

在20℃下保存24h和25℃下保存14h时,难以获得形态正常的GV期卵;体外受精获得的2细胞期胚经体外培养,总体上有64%的胚胎发育至扩张囊胚,未见有保存温度和保存时间的显著影响,且利用在15℃保存8h后的GV卵获得2细胞期胚的移植获得正常新生小鼠。

The three types of reconstructed embryos(reconstructed embryo of goat-rabbit, goat-bovine and goat-goat) were produced respectively by nuclear transfer using goat ear firbroblast cells as donors and rabbit, bovine and goat ooctyes as recipients, and the factors of cytoplast environments influencing cloned embryo development in vitro, cytoplast effect in nuclear transfer, the methods of transferring cloned embryo and the effects of pregnancy factor on implantation of cloned embryo were studied in this experiment, in order to supply basis for solving the difficulty of implantation of inter-species cloned embryo in recipient and improving the efficiency of cloning.

本试验以波尔山羊耳成纤维细胞为供体,分别以牛、羊、兔的卵母细胞为受体进行体细胞核移植,构建了山羊-兔、山羊-牛和山羊-山羊三种重构胚。研究了不同的胞质环境对重构胚体外发育的影响与核移植中的胞质效应,并对异种克隆胚胎采用了去透明带移植和配种后再移植的方法,探讨移植方法和妊娠因子对异种克隆胚胎在受体动物体内发育的影响,旨在为解决异种克隆胚移植不易着床发育的难题和为提高动物克隆效率提供理论依据。

The experiment results were as following:All cytoplast recipients derived from oocytes of rabbit, bovine and goat can support early development of cloned embryo, the fusion rate of reconstructed embryos of goat-bovine and goat-rabbit were 59.91% and 74.10%, their cleaved rate were 57.48% and 72.57%, blastocyst rate were 9.59% and18.06% respectively, and the fusion of reconstructed embryos of goat-rabbit and goat-goat were 60.01% and 74.10%, their cleaved rate were 56.68% and 72.57%, blastocyst rate were 11.76% and18.06% respectively.

试验获得了如下结果:1。以山羊耳成纤维细胞为供体,以牛、羊、兔卵母细胞做为胞质受体构建重构胚,并经体外培养,发现不同的胞质受体均能支持重构胚的早期发育,但受体胞质对重构卵的重构胚早期发育速度和卵裂率均有显著影响。

There are commonly eight nuclei in the embryo sac: the egg apparatus at the micropylar end, made up of an gee nucleus and two synergid nuclei; three antipodal cells at the oppsite chalazal end that probably aid embryo nourishment; and two polar nuclei in the center that fuse to form the primary endosperm nucleus.

通常胚囊中有8个核,卵器在珠孔端,由卵和两个助细胞组成;3个反足细胞在合点端,可能为胚胎提供营养;胚囊中央有2个极核,融合在一起形成最初的胚乳核。

In vitro, ES cells can spontaneously differentiate into embryoid bodies containing derivatives of three germ layers.

在体外,ES细胞可自发分化为含有内胚层、中胚层、外胚层来源的多种组织和细胞的拟胚体。

The embryonic vessels failed to invade into the labyrinthine layer of placenta, which impaired the embryonic-maternal vascular connection. These defects could not be rescued by wild-type tetraploid blastocysts, excluding the possibility that they were due to the extraembryonic tissues.

组织免疫组化分析结果显示:毛细血管腔异常扩张,排列紊乱,不能形成大血管及细致有序的血管网络;胚外中胚层来源的卵黄囊脏层扁平上皮细胞形态变圆,与内皮细胞连接受损;胚胎血管不能侵入胎盘迷路层,胚体与母体血管连接受损。

The results show the Boer goat oocyte and pre-implantation embryo are telomerase positive. According to the densitometry of bands under the CCD imagine system, the total telomere repeats product generated of oocytes, 4-cell, 8-cell, morulae and blastocyst are 25.348, 273.832, 56.117, 251.118, 519.46, respectively.

结果表明波尔山羊卵母细胞和早期胚胎都是端粒酶阳性;依据电泳条带在凝胶成像系统下的光密度计算相对总产品产量定量比较发现,卵母细胞最低为25.348,4-细胞为273.832,至8-细胞又降低到56.117,随后快速升高,桑椹胚为251.111,囊胚端粒酶活性最高为519.46。

The tetrad of megaspores was linear shaped, with one of them being functional.

锥栗胚胎为蓼型,功能大孢子发育成熟时共具有七个细胞八个细胞核,通过双受精作用,产生胚和胚乳,胚胎发育经历球形胚、心形胚、鱼雷形胚到子叶胚的过程。

objective the aim of this study is to investigate the expression and the distribution of the nerve growth factor during the period of neural tube development of human embryo.method early development of neural tube was studied in human embryos about 35 gestational days by using immunocytochemical abc technique.result there were ngf immuno-positive substances in the cytoplasm and nuclei of neuroepithelial cells in the ventricular zones of neural tube.in the intermediate zone of neural tube,ngf immunoreactivity was detected in the nuclei of some neurons,or the processes of other neurons which contained no ngf-immunoreactive substances in their nuclei;the expression pattern of ngf in the marginal zone of neural tube was similar to that of the intermediate zone.the density of ngf-immunorecative particles was higher on the rostrum side of neural tube than on the caudal side.the ngf immuno-positive cells were also observed among the somites of embryo under the neural tube.conclusion these results suggest that ngf was an important signal molecule to induce neural tube differentiation,and that ngf may play a significant role in regulation of the biological function of neurons in developing neural tube.

目的 研究捷安肽素的抗真菌作用机理。方法采用形态学方法和同位素标记法。显微形态观察经捷安肽素处理后的供试真菌的形态学变化。进一步采用14c同位素标记的特异底物&尿苷二磷酸-(14c)-葡萄糖&示踪,研究捷安肽素对真菌(1,3)-β-d-葡聚糖合成酶活性反应的影响。结果研究神经生长因子在早期人胚神经管发育过程中的定位表达。方法采用免疫细胞化学 abc法染色,研究35天人胚的发育情况。结果在人胚神经管的室管带中,神经元的细胞质和细胞核ngf免疫反应阳性;在中间带,一部分神经元的细胞核ngf免疫反应阳性,另外一部分神经元的细胞核ngf免疫反应阴性,而其突起ngf免疫反应阳性;在边缘带ngf的表达与中间带相似。在神经管的头侧ngf阳性反应较强,神经管的尾侧ngf阳性反应较弱。结论 ngf在人胚神经管免疫反应阳性,表明ngf可能是诱导神经管分化发育的重要信号分子,提示ngf可能在人胚神经管的发育中具有十分重要的作用。神经生长因子;人胚;神经管;发育

Oocyte samples from one group were collected to detect the presence and integration of HBV DNA within cells and chromosomes using PCR, Southern blot, dot hybridization and fluorescence in situ hybridization. The female animals from another group were mated with their normal males, respectively. Their zygotes, 2-cell embryos were collected to detect the integration of HBV DNA in the female pronuclei of zygotes and the replication and expression of HBV genes in the 2-cell embryos using FISH, RT-PCR and immunofluoresence assay.(1) PCR detected positive bands in the tested oocyte samples fromgoldon hamster and mice. Southern blot revealed clear hybridization signals in PCR products.

研究用金黄地鼠和小鼠建立实验动物模型:将卵巢内注射HBV DNA的实验动物分成两组,一组注射后进行超排卵,收集卵巢和输卵管的卵母细胞,用PCR、Southern杂交,斑点杂交和荧光原位杂交(fluorescence in situ hybridization、FISH)检测HBV在卵母细胞内的存在和染色体上的整合;另一组超排雌鼠与正常雄鼠合笼,收集受精卵和2-细胞胚,用FISH、RT-PCR和免疫荧光检测技术分别研究HBV基因在受精卵雌原核上的整合以及在2-细胞胚中的复制与表达。

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