首页> 外国专利> CRISPR SYSTEM AND USE THEREOF IN PREPARATION OF SEVERE-IMMUNODEFICIENCY CLONED PIG NUCLEAR DONOR CELLS WITH MULTIPLE GENES JOINTLY KNOCKED OUT

CRISPR SYSTEM AND USE THEREOF IN PREPARATION OF SEVERE-IMMUNODEFICIENCY CLONED PIG NUCLEAR DONOR CELLS WITH MULTIPLE GENES JOINTLY KNOCKED OUT

机译:CRISPR系统及其在制备联合敲除多个基因的严重免疫缺陷克隆猪核供体细胞中的应用

摘要

Provided are a CRISPR system and the use thereof in the preparation of severe-immunodeficiency cloned pig nuclear donor cells with multiple genes jointly knocked out. Provided are a method for preparing severe-immunodeficiency pig-derived recombinant cells with four genes, i.e. the ADA gene, the DQA gene, the DRA gene and the IL2RG gene, jointly knocked out; a CRISPR system; a combination of sgRNAs; a combination of plasmids; and a kit, wherein the combination of sgRNAs is composed of sgRNAADA-g7 as shown in SEQ ID NO: 11, sgRNADQA-gn2 as shown in SEQ ID NO: 21, sgRNADRA-g1 as shown in SEQ ID NO: 28 and sgRNAIL2RG-g7 as shown in SEQ ID NO: 40, and can be used for preparing recombinant cells, immunodeficiency animal models and immunodeficiency animal cell models.
机译:本发明提供一种CRISPR系统及其在制备联合敲除多个基因的严重免疫缺陷克隆猪核供体细胞中的用途。本发明提供了一种制备联合敲除ADA基因、DQA基因、DRA基因和IL2RG基因四种基因的严重免疫缺陷猪源重组细胞的方法;CRISPR系统;sgRNA的组合;质粒的组合;以及试剂盒,其中SgRNA的组合由SEQ ID NO:11所示的SgRNADA-g7、SEQ ID NO:21所示的sgRNADQA-gn2、SEQ ID NO:28所示的sgRNADRA-g1和SEQ ID NO:40所示的sgRNAIL2RG-g7组成,可用于制备重组细胞、免疫缺陷动物模型和免疫缺陷动物细胞模型。

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