Summary: The development of CRISPR-Cas9 screening techniques coupled with chemical inhibition of specific biological processes enables high-throughput investigation into many areas of molecular biology. We present a protocol to conduct ubiquitin proteasome system-specific chemical-genetic CRISPR-Cas9 screens in the human HAP1 cell line. This protocol can be adapted for use in other cell lines, with other compounds and types of treatments, and with any other sgRNA library.For complete details on the use and execution of this protocol, please refer to Hundley et al. (2021)
The cellular signalling process is a highly complex mechanism, involving multiple players, which tog...
Drug resistance is a major problem faced by tumor cell-targeted drugs. Currently, functional gene s...
CRISPR-Cas systems, widespread in bacteria and archaea, are mainly responsible for adaptive cellular...
As a powerful genome-editing tool, the clustered regularly interspaced short palindromic repeats (CR...
Components of the type II CRISPR-Cas complex in bacteria have been used successfully in eukaryotic c...
Characterizing variability in the extent and nature of responses to environmental exposures is a cri...
Abstract Background Large-scale genetic screening using CRISPR-Cas9 technology has emerged as a powe...
The ability to systematically disrupt genes serves as a powerful tool for understanding their functi...
Summary: Human pluripotent stem cells (hPSCs) generate a variety of disease-relevant cells that can ...
In recent years, sequence-specific clustered regularly interspaced short palindromic repeats (CRISPR...
In recent years, CRISPR/Cas9 technology has developed rapidly. With its accurate, fast, and simple e...
Zhao et al. performed phenotypic CRISPR screens to uncover genes and pathways that suppress DNA dama...
Forward genetic screens are powerful tools for the unbiased discovery and functional characterizatio...
The use of the bacterial-derived CRISPR/Cas9 genome editing system offers enormous opportunities to ...
Large-scale genomic analyses of tumor cells have revealed many genetic alterations present in cancer...
The cellular signalling process is a highly complex mechanism, involving multiple players, which tog...
Drug resistance is a major problem faced by tumor cell-targeted drugs. Currently, functional gene s...
CRISPR-Cas systems, widespread in bacteria and archaea, are mainly responsible for adaptive cellular...
As a powerful genome-editing tool, the clustered regularly interspaced short palindromic repeats (CR...
Components of the type II CRISPR-Cas complex in bacteria have been used successfully in eukaryotic c...
Characterizing variability in the extent and nature of responses to environmental exposures is a cri...
Abstract Background Large-scale genetic screening using CRISPR-Cas9 technology has emerged as a powe...
The ability to systematically disrupt genes serves as a powerful tool for understanding their functi...
Summary: Human pluripotent stem cells (hPSCs) generate a variety of disease-relevant cells that can ...
In recent years, sequence-specific clustered regularly interspaced short palindromic repeats (CRISPR...
In recent years, CRISPR/Cas9 technology has developed rapidly. With its accurate, fast, and simple e...
Zhao et al. performed phenotypic CRISPR screens to uncover genes and pathways that suppress DNA dama...
Forward genetic screens are powerful tools for the unbiased discovery and functional characterizatio...
The use of the bacterial-derived CRISPR/Cas9 genome editing system offers enormous opportunities to ...
Large-scale genomic analyses of tumor cells have revealed many genetic alterations present in cancer...
The cellular signalling process is a highly complex mechanism, involving multiple players, which tog...
Drug resistance is a major problem faced by tumor cell-targeted drugs. Currently, functional gene s...
CRISPR-Cas systems, widespread in bacteria and archaea, are mainly responsible for adaptive cellular...