官方服务：
资源简介：
CRISPR-cas9 mutagenesis plasmid Tn916 oriT plasmid pKM126, complete sequence
应用场景：
创建时间：
2022-06-10
相关数据集
Crystal structure of xCas9 P411T
Crystal structure of xCas9 P411T Descriptor: CRISPR-associated endonuclease Cas9/Csn1 Authors: Bao, R, Liu, H.Y, Luo, Y.Z, Song, Y.J. Deposit date: 2021-09-29 Release date: 2022-04-06 Last modified: 2
Protein Data Bank Japan2023-11-29 更新50
Additional file 6 of Minimal genome-wide human CRISPR-Cas9 library
Additional file 6: Table S5. Raw counts of the CRISPR-Cas9 screens at different guide coverage performed in KM-12 cancer cell line.
Figshare2021-01-23 更新30
Cloning and stable maintenance of DNA fragments over 300 kb in Escherichia coli with conventional plasmid-based vectors.
Bacterial artificial chromosome (BAC) and P1-derived artificial chromosome (PAC) systems were previously developed for cloning of very large eukaryotic DNA fragments in bacteria. We report the feasibi
PubMed Central1998-11-01 更新10
APOBEC3s induce mutations during the repair of CRISPR-Cas9-generated DNA breaks.
APOBEC-AID family of cytidine deaminase prefers single-stranded nucleic acids for cytidine to uracil deamination. Single-stranded nucleic acids are commonly involved in the DNA repair system for break
NIAID Data Ecosystem40
Bacterial strains and plasmids used in this study
Bacterial strains and plasmids used in this study
NIAID Data Ecosystem20
