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siRNA knockout assay method and constructs

机译:siRNA敲除测定方法和构建体

摘要

Isolated polynucleotides, and vectors including the same, are disclosed as useful for down-regulation of specific RNA in cells, including a first sequence of about 17 to about 23 nucleotides, complementary to said RNA, and linked to a second sequence capable of forming a loop when said second sequence is RNA. The polynucleotides include self-complementing single-stranded polynucleotides, including a third sequence linked by said second sequence where all nucleotides in said first and said third sequences are complementary. Functional genomic, diagnostic and therapeutic methods are disclosed that involve reducing the amount of a unique RNA sequence in cells using a vector encoding the self-complementing polynucleotide including a first sequence complementary to said RNA sequence. Methods are also disclosed for preparing the polynucleotides, vectors, libraries of vectors, and the temporary knock-down of proteins, such as lethal proteins, during virus or recombinant protein production.
机译:公开了分离的多核苷酸和包含该多核苷酸的载体可用于下调细胞中的特定RNA,包括与所述RNA互补并与能够形成DNA的第二序列连接的约17至约23个核苷酸的第一序列。当所述第二序列是RNA时,该环循环。所述多核苷酸包括自我互补的单链多核苷酸,包括由所述第二序列连接的第三序列,其中所述第一和所述第三序列中的所有核苷酸是互补的。公开了功能基因组学,诊断和治疗方法,其涉及使用编码包含与所述RNA序列互补的第一序列的自互补多核苷酸的载体,减少细胞中独特RNA序列的量。还公开了在病毒或重组蛋白生产过程中用于制备多核苷酸,载体,载体文库以及蛋白(例如致死蛋白)的临时敲除的方法。

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