细胞瞬时转染/稳定转染
/* Style Definitions */ table.MsoNormalTable {mso-style-name:普通表格; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-nosh
MTT实验技术服务
/* Style Definitions */ table.MsoNormalTable {mso-style-name:普通表格; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-st
iPSC基因编辑
参考文献 Induction of Pluripotent Stem Cells from Mouse Embryonic and Adult Fibroblast Cultures by Defined Factors iPSC-derived lung and lung cancer
基因敲入细胞
Modulation of cell cycle increases CRISPR-mediated homology-directed DNA repair CLASH enables large-scale parallel knock-in for
基因点突变细胞
参考文献 Generation of Human Isogenic Induced Pluripotent Stem Cell Lines with CRISPR Prime Editing Structural basis for pegRNA-guided rev
基因敲除细胞/ko细胞
艾迪基因基于自主研发的EditXTM基因编辑平台，采用优化升级的CRISPR/Cas9系统，可根据基因与细胞、实验目的，制定合适的敲除策略和方案，可高效地构建符合需求的基因敲除细胞模型。 参考文献 】Bromodomain protein BRD4 promotes ce
过表达稳转株
High Expression of SRSF10 Promotes Colorectal Cancer Progression by Aberrant Alternative Splicing of RFC5 The alteration of LBX1 expressio