| Literature DB >> 28205168 |
Ximing Du1, Ivan Lukmantara1, Hongyuan Yang2.
Abstract
Generating a cholesterol storage phenotype of Niemann-Pick Type C (NPC) disease is important for investigating the mechanisms of intracellular cholesterol trafficking, as well as screening drugs for potential treatment of NPC disease. The use of the CRISPR/Cas9 technology to knockout specific genes within the genome of mammals has become routine in the past few years. Here, we describe a protocol for producing a cellular NPC cholesterol storage phenotype in HeLa cells using the CRISPR-Cas9 system to disrupt the NPC1 gene. The protocol details the steps for single guide RNA oligo cloning, cell colony selection, and cell line verification by filipin staining and immunoblotting.Entities:
Keywords: CRISPR; Cas9; Cholesterol; Filipin; NPC1; sgRNA
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Year: 2017 PMID: 28205168 DOI: 10.1007/978-1-4939-6875-6_7
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745