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Methods and kits for analysis of chromosomal rearrangements associated with leukemia

机译:分析与白血病有关的染色体重排的方法和试剂盒

摘要

The invention relates to kits and methods for panhandle PCR amplification of a region of DNA having an unknown nucleotide sequence, wherein the region flanks a region of a leukemia-associated gene having a known nucleotide sequence in a human patient. Amplification of an unknown region flanking a known region of a leukemia-associated gene permits identification of a translocation partner of the gene or identification of a duplicated sequence within the gene. The invention further relates to kits useful for performing the methods of the invention, to an isolated polynucleotide, and to primers derived from such an isolated polynucleotide.
机译:本发明涉及试剂盒和方法,该试剂盒和方法用于在人患者中PCR扩增具有未知核苷酸序列的DNA区域,其中该区域位于白血病相关基因的具有已知核苷酸序列的区域的侧面。白血病相关基因的已知区域侧翼的未知区域的扩增允许鉴定基因的易位伴侣或鉴定基因内的重复序列。本发明进一步涉及可用于实施本发明方法的试剂盒,分离的多核苷酸以及衍生自此类分离的多核苷酸的引物。

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