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1.Methods Human specific Y chromosome satellite DNA CEPY and 17 chromosome satellite DNA p17H8 were used as probes for IFISH. The peripheral blood samples from 2 goats transplanted with human male hematopoietic stem cells (HSC), 1 normal negative goat and 1 normal man were analyzed.
方法 采用人特异Y染色体卫星DNA探针CEPY和 17号染色体卫星DNA探针p17H8对两头移植人男性造血干细胞 (hematopoieticstemcell,HSC)的人 /山羊嵌合模型、1头正常阴性山羊和 1名正常人男性的外周血进行IFISH分析。收藏指正
2.Objective To find an effective method which can be used for studying variation of X chromosome centromeric alpha satellite DNA.
目的: 以Klinefelter综合征患者为研究对象,从DNA分子水平建立一种研究X染色体着丝粒区α-卫星DNA变异的有效方法,以探讨X染色体非整倍体患者的X染色体着丝粒区α-卫星DNA的变异与染色体不分离的关系。收藏指正
3.In the S-chromosomes present in TAI7045, there were one satellited chromosome pair, in which a large satellite was present on the short arm and the hybridization signal of S genome was detected over the satellite. The molecular karyotype of TAI7045 revealed by GISH could be depicted 2n = 56 = 42 wheat + 6 S + 2 S-sat + 4 Es + 2 EVS.
而且所含的S组染色体中有1对为大随体染色体,其染色体组成为2n=56=42 wheat+6S+2S-sat+4E~S+2S/E~S.收藏指正
4.Variation of alpha satellite DNA in X chromosome centric region of Klinefelter (syndrome)
Klinefelter综合征X染色体着丝粒区α-卫星DNA变异收藏指正
5.Relation between Variation of Centromeric Alpha Satellite DNA on Human X Chromosome and Aneuploidy
人类X染色体着丝粒区α卫星DNA变异与非整倍体关系研究收藏指正
6.Methods: Biotin labeled alpha satellite X chromosome DNA(pBamX7) probe and Digoxigenin labeled Y chromosome long arm terminal repetitive sequence (pY3. 4) probe in situ hybridized with pre-treated slides of peripheral blood chromosome and in-terphase nucleus.
方法:以Biotin标记的X染色体α-卫星DNA(pBamX7)探针和以Digoxigenin标记的Y染色体长臂末端重复顺序(pY3.4)探针与经处理的标本同时进行外周血染色体及间期细胞核的原位杂交,分别用Avidin-FITC和Rhodamine-FITC及其Anti-avidin进行信号的检测与放大,DAPI复染。收藏指正
7.Contrasting the normal karyotype of the diploid Chinese cabbage-pe-tsai,the 25S rDNA hybridization signals were located near the end of 1L,the central section of 2L,the centromere region of 3L and 4L,and the satellite of chromosome 10,respectively.
对应于大白菜中期染色体形态图,确定5对25S rDNA信号分别分布在大白菜1号染色体长臂(1L)的近末端,2号染色体长臂(2L)的近中部,3号和4号染色体长臂(3L、4L)的近着丝点处和10号染色体的随体上,信号强度为10号>2号>3号和4号>1号;收藏指正
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