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Simultaneous isolation and quantify dna

机译:同时隔离和定量dna

摘要

The present invention provides methods for isolating a defined quantity of DNA target material from other substances in a medium. The method may be carried out using a known quantity of a silica-containing solid support, such as silica magnetic particles, having a definable capacity for reversibly binding DNA target material, and DNA target material in excess of the binding capacity of the particles. The methods of the present invention involve forming a complex of the silica magnetic particles and the DNA target material in a mixture of the medium and particles, and separating the complex from the mixture using external magnetic force. The DNA target material may then be eluted from the complex. The quantity of DNA target material eluted may be determined based on a calibration model. The methods of the present invention permit isolation of DNA target material which is within a known quantity range. The methods of the invention eliminate the step of quantitating purified biological samples prior to further processing, such as amplification, Short Tandem Repeat (STR) analysis, and DNA sequencing. Samples of the DNA target materials may be obtained from liquid or solid media, such as liquid blood or paper.
机译:本发明提供了从培养基中的其他物质中分离出一定量的DNA靶物质的方法。可以使用已知量的具有可逆结合DNA靶物质的可定义能力的已知量的含二氧化硅的固体载体,例如二氧化硅磁性颗粒和超过颗粒的结合能力的DNA靶物质来进行该方法。本发明的方法包括在介质和颗粒的混合物中形成二氧化硅磁性颗粒和DNA靶材料的复合物,并使用外部磁力从混合物中分离复合物。然后可以从复合物中洗脱DNA靶物质。可以基于校准模型确定洗脱的DNA靶物质的量。本发明的方法允许分离在已知量范围内的DNA靶物质。本发明的方法省去了在进一步处理之前对纯化的生物样品进行定量的步骤,所述进一步的处理例如扩增,短串联重复(STR)分析和DNA测序。 DNA靶材料的样品可以从液体或固体介质如液体血液或纸获得。

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