期刊文献+
共找到7篇文章
< 1 >
每页显示 20 50 100
小鼠2细胞期胚胎移植方法的探讨 被引量:3
1
作者 左琴 范昌发 +1 位作者 胡培丽 岳秉飞 《中国比较医学杂志》 CAS 2007年第8期I0027-I0029,共3页
目的以近交系C57BL/6J小鼠作为供体胚小鼠,封闭群ICR小鼠及昆明鼠作为假孕体,对2细胞期的胚胎移植方法和假孕鼠品系进行对比探讨。方法经超数排卵的C57BL/6J雌鼠于正常雄鼠交配,取受精卵,培养到2细胞期,进行输卵管伞移植和输卵管壁移植... 目的以近交系C57BL/6J小鼠作为供体胚小鼠,封闭群ICR小鼠及昆明鼠作为假孕体,对2细胞期的胚胎移植方法和假孕鼠品系进行对比探讨。方法经超数排卵的C57BL/6J雌鼠于正常雄鼠交配,取受精卵,培养到2细胞期,进行输卵管伞移植和输卵管壁移植,妊娠产仔。结果从KM为假孕鼠,对2细胞期胚胎进行的输卵管壁移植的妊娠数量最多18只,90%的妊娠率,产仔数最多188只,产仔率达34.8%。结论输卵管壁移植的技术简单易行具有较高的妊娠率及产仔率。 展开更多
关键词 近交系小鼠 2细胞期胚胎 胚胎移植
下载PDF
Cdc25B蛋白过表达可使小鼠胚胎突破2-细胞期阻滞 被引量:2
2
作者 崔城 汤浩 于秉治 《中国应用生理学杂志》 CAS CSCD 北大核心 2008年第1期99-103,共5页
目的:探讨Cdc25B蛋白过表达对小鼠2-细胞期胚胎发育的影响。方法:利用体外转录试剂盒将Cdc25B转录成mRNA,将mRNA显微注射入小鼠2-细胞期胚胎中,观察胚胎发育情况和卵裂率。用蛋白激酶活性测定方法和Western印迹分别检测Cdc25B蛋白过表... 目的:探讨Cdc25B蛋白过表达对小鼠2-细胞期胚胎发育的影响。方法:利用体外转录试剂盒将Cdc25B转录成mRNA,将mRNA显微注射入小鼠2-细胞期胚胎中,观察胚胎发育情况和卵裂率。用蛋白激酶活性测定方法和Western印迹分别检测Cdc25B蛋白过表达小鼠胚胎MPF的活性及Cdc2-Tyr15的磷酸化状态。结果:hCG后48 h,mRNA注射组有超过40%的2-细胞期胚胎分裂到4-细胞期而对照组仍停留在2-细胞期;激酶活性测定显示注射Cdc25B mRNA后,MPF的活性显著升高;Cdc2-Tyr15的磷酸化状态变化与激酶活性测定结果一致。结论:Cdc25B蛋白过表达可以激活有丝分裂促进因子(MPF),从而使小鼠2-细胞期胚胎突破2-细胞期阻滞,发育到4-细胞期。 展开更多
关键词 小鼠2-细胞胚胎 CDC25B MPF
下载PDF
用小鼠单个MⅡ卵和2-细胞期胚胎构建cDNA文库
3
作者 李文雍 王荣 《安徽师范大学学报(自然科学版)》 CAS 2003年第4期370-373,共4页
阶段特异性cDNA文库的构建和筛选是一种分离和克隆早期胚胎特异表达基因的有效方法.本研究利用小鼠单个MⅡ卵母细胞及发育至2-细胞的胚胎分别构建了cDNA文库.滴度分别为:6.5×106、7.2×107,基因片段平均长度为250-1500bp并用β... 阶段特异性cDNA文库的构建和筛选是一种分离和克隆早期胚胎特异表达基因的有效方法.本研究利用小鼠单个MⅡ卵母细胞及发育至2-细胞的胚胎分别构建了cDNA文库.滴度分别为:6.5×106、7.2×107,基因片段平均长度为250-1500bp并用β-actin验证了文库的可靠性.这种利用单胚胎构建cDNA文库的方法,不仅解决了胚胎研究材料受限制的问题,而且在材料的发育时间上更加精确,更能反映胚胎发育的规律,是研究早期胚胎发育基因表达以及克隆胚胎发育相关基因的一种有效手段. 展开更多
关键词 小鼠 CDNA文库 MⅡ卵 2-细胞胚胎 植入前胚胎 阶段特异性基因表达
下载PDF
C57-ras癌症转基因小鼠模型胚胎冷冻保种技术研究 被引量:2
4
作者 左琴 刘甦苏 +3 位作者 周舒雅 刘佐民 王金恒 范昌发 《中国比较医学杂志》 CAS 2013年第5期34-37,共4页
目的建立C57-ras癌症转基因小鼠模型胚胎的冷冻保种技术。方法通过直接收集体内发育的2-细胞胚或者通过体外受精方法获得2-细胞胚,采用玻璃化冷冻法冷冻、复苏、移植,后代经PCR检测。结果体内发育至2细胞期胚胎90枚,解冻后的平均复苏率... 目的建立C57-ras癌症转基因小鼠模型胚胎的冷冻保种技术。方法通过直接收集体内发育的2-细胞胚或者通过体外受精方法获得2-细胞胚,采用玻璃化冷冻法冷冻、复苏、移植,后代经PCR检测。结果体内发育至2细胞期胚胎90枚,解冻后的平均复苏率是67.78%,移植产仔率是21.31%,后代的阳性率是23.08%;体外受精的2细胞期胚胎203枚,解冻复苏60枚,平均复苏率是63.33%,移植产仔率是15.78%,后代的阳性率是33.33%。结论两种胚胎冷冻途径均获得了C57-ras癌症转基因动物模型阳性小鼠,建立了该模型动物的低温保存方法。 展开更多
关键词 C57-ras转基因小鼠 体外受精 胚胎冷冻 2细胞期胚胎
下载PDF
小鼠胚胎单侧与双侧输卵管移植的结果比较 被引量:1
5
作者 王芊芊 陈瑜 《实验动物与比较医学》 CAS 2012年第5期414-415,共2页
目的比较小鼠胚胎移植入单侧与双侧输卵管的差异,探索最佳的胚胎移植方法。方法选用C57BL/6J小鼠作为供体小鼠,取1.5d胚胎即2-细胞期胚胎分别采用单侧和双侧输卵管移植ICR假孕雌鼠,统计仔鼠出生率。结果经单侧输卵管移植和双侧输... 目的比较小鼠胚胎移植入单侧与双侧输卵管的差异,探索最佳的胚胎移植方法。方法选用C57BL/6J小鼠作为供体小鼠,取1.5d胚胎即2-细胞期胚胎分别采用单侧和双侧输卵管移植ICR假孕雌鼠,统计仔鼠出生率。结果经单侧输卵管移植和双侧输卵管移植后假孕雌鼠的妊娠率均为100%,产仔率分别为32.5%和34.7%。结论小鼠2-细胞期胚胎经输卵管双侧移植较单侧移植的产仔率略高,但无显著差异。 展开更多
关键词 小鼠 2-细胞胚胎 单侧移植 双侧移植 产仔率
下载PDF
Antibodies against the C-terminal peptide of rabbit oviductin inhibit mouse early embryo development to pass 2-cell stage 被引量:8
6
作者 PAN YONG, ZHENG GU, JIN PING LUO, JUN Ru WANG, JIA KE TSO National Laboratory of Contraceptives and Devices Research, Shanghai Institute of Planned Parenthood Research, 21.40 Xietu Road, Shanghai 200032, China 《Cell Research》 SCIE CAS CSCD 2002年第1期69-78,共10页
A full-length rabbit oviductin cDNA(1909bp) was cloned. It consists of a 5’-UTR of 52bp, an open reading frame (ORF) of 1374bp and a 3’-UTR of 483bp and has more than 80% homology with that of other mammal oviductin... A full-length rabbit oviductin cDNA(1909bp) was cloned. It consists of a 5’-UTR of 52bp, an open reading frame (ORF) of 1374bp and a 3’-UTR of 483bp and has more than 80% homology with that of other mammal oviductins. N-terminal peptide (NTP) (384 residues) and C-terminal peptide (CTP) (73 residues) of deduced protein precursor has about 80% and 50% identity with that of other mammals respectively. Fusion proteins GST-NTP 368(1R-368N)and GST-CTP73 (369F-441A) were expressed and purified. NH2-terminal of CTP sequencing reveals that the purified protein is consistent with the deduced one. In order to study the function of NTP and CTP the mouse anti-NTP and rabbit anti-CTP antisera were prepared. Tissue-specific (skeleton muscle, oviduct, uterus, ovary, liver, heart and brain) analysis indicated that rabbit oviductin was only found in oviduct. The conditioned medium derived from the rabbit oviduct mucosa epithelial cells has a function of overcoming the early embryonic development block of Kunming mous e cultured in vitro. Anti-CTP antiserum could totally inhibit the early embryo development at 2-cell stage cultured in the conditioned culture medium, but anti-NTP antiserum couldn’t. There was a positive relationship between the ratio of early embryos at development block and the dosage of anti-CTP antiserum added in the conditioned culture medium. These results suggest that oviductin has a function not only on fertilization, but also on the release of early embryonic development block, and the later function domain of rabbit oviductin may be situate in its C-terminal. 展开更多
关键词 Rabbit oviductin C-terminal peptide early embryo DEVELOPMENT loss of function.
下载PDF
Effect of antikeratin microinjection on the embryonic development of Xenopus laevis
7
作者 YUHAOJIAN JINGWUXIE 《Cell Research》 SCIE CAS CSCD 1993年第2期147-156,共10页
Anti-keratin monoclonal antibody AF5 was introduced into fertilized eggs of Xenopus laevis., and its effects on embryonic development were studied. Survival rate of the antikeratin-injected embryos was much lower (onl... Anti-keratin monoclonal antibody AF5 was introduced into fertilized eggs of Xenopus laevis., and its effects on embryonic development were studied. Survival rate of the antikeratin-injected embryos was much lower (only 35.76% at gastrula) than that of the control (74.85% at gastrula), in which embryos were injected with mouse IgG. Most of survivors in the experimental series showed aberrant external appearance. On the other hand, in cleavage stage, ie 2-7 h after fertilization, immunohistochemi-cal staining of embryos showed that the experimental embryos were mostly keratin negative, while embryos of the control ones were keratin positive. When introducing this antikeratin into one cell of a 2-cell embryo, only the unin-jected half of the embryo continued its development while the other half could not develop at all. These results suggested that intact keratin cytoskeleton in early embryos is indispensable to the embryonic development of Xenopus laevis. 展开更多
关键词 Xenopus laevis fertilized egg KERATIN CYTOSKELETON monoclonal antibody microinjection.
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部