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41.
We have developed technologies that simplify genomic library construction and screening, substantially reducing both the time and the cost associated with traditional library screening methods and facilitating the generation of gene-targeting constructs. By taking advantage of homologous recombination in Escherichia coli, we were able to use as little as 80 bp of total sequence homology to screen for a specific gene from a genomic library in plasmid or phage form. This method, called recombination cloning (REC), takes only a few days instead of the several weeks required for traditional plaque-lift methods. In addition, because every clone in the mouse genomic library we have constructed has a negative selection marker adjacent to the genomic insert, REC screening can generate gene-targeting vectors in one step, from library screening to finished construct. Conditional targeting constructs can be generated easily with minimal additional manipulation. 相似文献
42.
研究了硼钛复合纤维在拉伸过程中的行为,结果表明:复合纤维的变形是由纤维的弹性应变与基体的弹塑性应变复合迭加而成,并且在纤维与基体结合十分牢固,基体组元体积分数又较少的情况下,复合纤维表现为高强度,高弹性模量及低塑性,将试验结果同理论计算模型进行了比较,所得结果基本一致。 相似文献
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以结构力学理论为依据,以有限元SAP5程序为计算手段,提出了一种直线振动筛侧板的动力学强度的计算方法,并分析了这类振动筛在侧板上产生裂纹的原因. 相似文献
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Glycine: a new anti-inflammatory immunonutrient 总被引:7,自引:0,他引:7
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Human hepatitis B vaccine from recombinant yeast 总被引:22,自引:0,他引:22
W J McAleer E B Buynak R Z Maigetter D E Wampler W J Miller M R Hilleman 《Nature》1984,307(5947):178-180
The worldwide importance of human hepatitis B virus infection and the toll it takes in chronic liver disease, cirrhosis and hepatocarcinoma, make it imperative that a vaccine be developed for worldwide application. Human hepatitis B vaccines are presently prepared using hepatitis B surface antigen (HBsAg) that is purified from the plasma of human carriers of hepatitis B virus infection. The preparation of hepatitis B vaccine from a human source is restricted by the available supply of infected human plasma and by the need to apply stringent processes that purify the antigen and render it free of infectious hepatitis B virus and other possible living agents that might be present in the plasma. Joint efforts between our laboratories and those of Drs W. Rutter and B. Hall led to the preparation of vectors carrying the DNA sequence for HBsAg and antigen expression in the yeast Saccharomyces cerevisiae. Here we describe the development of hepatitis B vaccine of yeast cell origin. HBsAg of subtype adw was produced in recombinant yeast cell culture, and the purified antigen in alum formulation stimulated production of antibody in mice, grivet monkeys and chimpanzees. Vaccinated chimpanzees were totally protected when challenged intravenously with either homologous or heterologous subtype adr and ayw virus of human serum source. This is the first example of a vaccine produced from recombinant cells which is effective against a human viral infection. 相似文献
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