排序方式: 共有36条查询结果,搜索用时 15 毫秒
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GC/MS法追踪摇头丸杂质体系 总被引:1,自引:0,他引:1
本文运用GS/MS的总离子流法,选择离子法,对南京地区常见的几种摇头丸进行全面分析,找出与合成途径相关的痕量杂质,根据杂质情况初步确定其合成途径. 相似文献
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吐哈盆地台南凹陷鲁克沁构造带中的北西走向断层受挤压强烈 ,封闭性好 ;而北东走向断层封闭性差 ,常成为油气运移的良好通道。由于本区断块圈闭的有效性差 ,故不具备大规模聚集稀油的条件 ,但对稠变到一定程度的稠油能起较好的封堵作用。鲁克沁构造带高粘重质油的形成是原油运移和成藏阶段双重稠变作用的结果 ,并且油气的聚集是一个动态的过程。随着原油的逐渐稠变 ,所需要的封堵条件逐渐降低 ,油气的聚集过程才趋于稳定。鲁克沁构造带构造后期变革主要表现在构造幅度的增大 ,而未发生强烈的断裂作用 ,因此 ,前侏罗系油藏得以完好地保存 相似文献
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L. Ebert 《Cellular and molecular life sciences : CMLS》1946,2(4):152-152
Ohne ZusammenfassungTätigkeit der Mathematisch-Naturwissenschaftl. Klasse im Jahre 1945 相似文献
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求取剩余油饱和度的一种实用方法 总被引:5,自引:4,他引:1
杨少春 《中国石油大学学报(自然科学版)》1998,(2)
分析了水驱油田地质、测井及开发动态特征,提出了用生产井含水率资料结合测井资料求取产层平均剩余油饱和度的方法。阐述了该方法的基本模型和计算过程,并以实例计算说明了这种方法的实际应用效果。结果表明,该方法操作简便、实用性强、计算结果可靠,且能准确反映储层的剩余油分布特征。这种方法也避免了水淹层混合液电阻率、岩电系数和水淹层电阻率求取值失真的影响。 相似文献
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MicroRNAs can generate thresholds in target gene expression 总被引:2,自引:0,他引:2
Mukherji S Ebert MS Zheng GX Tsang JS Sharp PA van Oudenaarden A 《Nature genetics》2011,43(9):854-859
MicroRNAs (miRNAs) are short, highly conserved noncoding RNA molecules that repress gene expression in a sequence-dependent manner. We performed single-cell measurements using quantitative fluorescence microscopy and flow cytometry to monitor a target gene's protein expression in the presence and absence of regulation by miRNA. We find that although the average level of repression is modest, in agreement with previous population-based measurements, the repression among individual cells varies dramatically. In particular, we show that regulation by miRNAs establishes a threshold level of target mRNA below which protein production is highly repressed. Near this threshold, protein expression responds sensitively to target mRNA input, consistent with a mathematical model of molecular titration. These results show that miRNAs can act both as a switch and as a fine-tuner of gene expression. 相似文献
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K. M. Ebert R. E. Hammer V. E. Papaioannou 《Cellular and molecular life sciences : CMLS》1985,41(9):1207-1209
Summary An easy and rapid method of counting the number of cells in the preimplantation mouse embryo is described. The procedure increases the speed with which large numbers of embryos can be processed using a simple squash technique. Cell numbers are determined by exposing the embryos to the fluorescent DNA-binding dye, Hoechst 33258, removing the zona pellucida and simply squashing the embryo and counting the number of fluorescent nuclei. An increase in fluorescent intensity and maintenance of nuclear conformation of the squashed preparations are greatly improved by the use of the non-ionic detergent Triton X-100. Viability of dye-treated fertilized one-cell and blastocyst stage embryos is maintained at least up to day 13 of pregnancy following transfer of the embryos to the uteri of pseudopregnant recipients. Additional uses for this staining technique are discussed.Acknowledgment. Financial support was provided by NIH Grant HDD-06210 (KME) and by Basil O'Connor Starter Research Grant No. 5-379 from the March of Dimes Birth Defects Foundation (VEP). We thank Steven Halpern for help with the photography and Jon Flax for expert technical assistance. 相似文献