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小鼠-牛体细胞种间核移植 总被引:1,自引:0,他引:1
本文探讨了小鼠-牛异质胚构建的简便方法及小鼠体细胞核在牛卵母细胞中重新编程的可能性。以牛的卵母细胞为细胞质供体,用去除透明带及徒手切割的方法去核,设定电压1.5 KV/cm,脉冲时间40μsec,与小鼠皮肤成纤维细胞进行电融合的融合率为67.44%,卵裂率为30.23%。融合细胞经离子酶素-6-DMAP激活,用微滴内压制做窝的方法培养小鼠皮肤成纤维细胞异质胚,异质胚的最终发育阶段为8细胞期。结果表明,去透明带牛卵母细胞经切割法去核,可用于小鼠异质胚构建;微滴内做窝的体外培养方法可避免无透明带胚胎的聚合。 相似文献
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【目的】探究广东本地及移民学龄儿童的饮食结构及肠道菌群分布的差异。【方法】以广东深圳为采样点,随机抽样选取48名广东本地儿童和34名移民儿童,进行膳食问卷调查和晨便采集。采用Mann-Whitney U test分析本地及移民儿童饮食因子摄入频率的差异,并使用Illumina Miseq高通量测序技术对儿童的肠道菌群进行测序分析。【结果】82例儿童的膳食模式大多以米饭为主食,搭配蔬菜、优质肉类以及水果。但本地儿童在复合碳水化合物、蔬菜、海产品方面有更高的摄入量(P<0.05),而移民儿童在水果、低脂牛奶、酸奶产品方面有更高的摄入量(P<0.05)。α多样性结果显示,移民组的Chao1指数(P<0.001)和Ace指数(P<0.001)均显著高于本地组。在菌属水平,本地儿童肠道普氏菌属(P=0.027)和副拟杆菌属(P=0.040)丰度显著高于移民组。LEfSe分析同样显示菌群的组间差异主要由本地组的普氏菌科、普氏菌属等造成。RDA结果提示,蔬菜和低脂牛奶的摄入水平显著影响本地儿童肠道菌群的分布,初步提示本地儿童的饮食习惯可能影响肠道普氏菌属和副拟杆菌属的丰度。【... 相似文献
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建立稳定的次黄嘌呤鸟嘌呤磷酸核糖转移酶(HGPRT)缺陷的Hela细胞系,为细胞融合相关研究和人源化单克隆抗体制备提供有利于筛选的亲本细胞。通过诱变剂N-甲基-N′-硝基-N-亚硝基胍(MNNG)对Hela细胞进行诱变,逐步提高培养基中6-巯基鸟嘌呤(6-TG)的浓度,筛选出对6-TG稳定耐受的细胞,在次黄嘌呤-氨基喋呤-胸腺嘧啶(hypoxanthine-aminopterin-thymidine,HAT)培养基中鉴定其敏感性,最后对筛选得到的Hela-HGPRT-进行生物学鉴定。在此基础上,将Hela-HGPRT-细胞系与人淋巴细胞融合,在HAT培养基中筛选杂交细胞。筛选得到了能够长期在含20μg/mL 6-TG培养基中生长的Hela-HGPRT-细胞,并且在HAT培养基中不能存活。Hela-HGPRT-细胞与人淋巴细胞成功融合,获得能够连续传代培养的杂交瘤细胞。经MNNG诱导和6-TG筛选,得到了稳定传代的Hela-HGPRT-细胞系,该细胞系可用于细胞融合相关研究。 相似文献
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北京市生态用地规划与管理对策 总被引:7,自引:0,他引:7
不合理土地开发加速了对自然生态系统的干扰和侵占,导致生态系统服务功能下降,危机区域生态安全,开展生态用地规划是构建区域生态安全格局的基础。合理规划和管理不同土地利用类型的数量和空间分布对区域可持续发展具有重要意义。目前我国广泛应用的土地利用分类体系主要以土地的社会经济属性为基础,忽视其生态属性,导致以提供生态系统服务为主、保障生态安全的土地缺乏保护机制,具有重要生态功能的土地得不到有效保护。以北京市为例,建立了北京市生态用地分类与规划的思路与程序,在明确北京市生态安全与生态系统服务功能的关系基础上分析了北京市生态系统服务功能重要性及其空间格局,并进行了北京市生态用地规划。研究规划了保障北京市生态安全的7类生态用地:地表水涵养与保护用地、地下水保护用地、生物多样性保护用地、水土保持用地、河流防护用地、公路防护用地和城市绿地,总面积5137.37km2,占北京市域面积的31.31%。最后从生态用地识别和划分、将生态用地融入土地利用分类体系、生态用地管理措施和对策3个方面探讨了生态用地规划和管理的方法与措施。研究结果为北京市土地利用规划和有效管理提供依据,也为其它地区的生态用地规划提供参考。 相似文献
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Cloned goats (Capra hircus) from adult ear cells 总被引:11,自引:0,他引:11
The average number of available oocytes recovered per ovary collected during the breeding season in dairy goats was 5.5 (1815/330). 66.17% (1201/1815) of oocytes extruded the first polar body after maturation in vitro for 20 h. 75.44% (906/1201) of matured oocytes with membrane evagination around the MII chromosomes were enucleated. Ear skin fibroblast cells were derived from an adult female dining Grey goat (C. hircus). The cells were cryopreserved in liquid nitrogen after passage 2. Thawed cells were further cultured for 3-6 passages and were subjected to serum starvation by 0.5% FBS for 2-10 d, then used as donor cells for nuclear transfer. 98.12% (889/906) of the enucleated oocytes were reconstructed by intracytoplasmic injection of karyoplast. The reconstructed embryos were activated by 5μ mol/L ionomycin for 4.5 min and further activated by culturing with 6-dimethylaminopurine (6-DMAP) for 3 h. After 36 h of culture in mCR1aaBF, 76.69% (645/841) of the cloned embryos cleaved. There were no signifi 相似文献
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Effects of different activation methods on the cleavage and in vitro development of bovine somatic cloned embryos constructed by intracytoplasmic nuclear injection were compared. The results show that the cleavage and in vitro development rate were not different significantly for constructed embryos cultured in 6-DMAP comparing with those in 6-DMAP + cytochalasin B (CCB) after activation with Ionomycin. Culture duration (3 to 4 h) in 6-DMAP or 6-DMAP + CCB had no significant effects on the cleavage and in vitro development ability of reconstructed embryos. CCB addition in the activation medium was benefit to the development of constructed embryos, although the effect wasn't significant. Within 1 to 4 h, the longer interval duration of nuclear injection and reconstructed embryo activation was, the higher cleavage and the blastocyst development rate of reconstructed embryos were. 相似文献
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