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Methods for detection of target molecules and molecular interactions between nucleic acid tags attached to binding entities specific for the target molecules of interest

机译:用于检测目标分子和附着于对目标目标分子特异的结合实体的核酸标签之间的分子相互作用的方法

摘要

Methods of detecting target molecules are described together with the interactions between target molecules based on interactions between proximally-bound nucleic acid tags. Reagent kits for use in such methods are also provided. Figure 3 illustrates an exchange of sequence between the nucleic acid tags that results in a previously unknown detectable sequence. Examples of such detectable sequences include nucleic acid amplification primer binding sites or RNA polymerase binding sites, i.e., promoters that allow detection of the sequence by amplification. The sequences that promote the exchange of sequence are shown as triangles. One system that could be used is the phage lambda-based site-specific recombination system. In this example, the attL and attR recombination sequences recombine in the presence of recombinase to generate attP and attB.
机译:描述了检测靶分子的方法以及基于近端结合的核酸标签之间相互作用的靶分子之间的相互作用。还提供了用于此类方法的试剂盒。图3示出了核酸标签之间的序列交换,其导致先前未知的可检测序列。这样的可检测序列的实例包括核酸扩增引物结合位点或RNA聚合酶结合位点,即允许通过扩增检测序列的启动子。促进序列交换的序列显示为三角形。可以使用的一种系统是基于噬菌体λ的位点特异性重组系统。在该实例中,attL和attR重组序列在重组酶存在下重组以产生attP和attB。

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