Autophagy related diseases explored with gene edited cell lines
As demonstrated by the 2016 Nobel Prize winner, Yoshinori Ohsumi, autophagy is a fundamental process vital to cellular health. The molecular processes and signalling pathways controlling autophagy include numerous autophagy-related (Atg) genes, important stress-inducible intracellular protein, such as p62/A170/SQSTM1 and autophagosome localizing proteins such as LC3, among many others making this a complex network of control
Gene deletion experiments in both mice and cell lines have implicated autophagy in the development of a number of diseases including; neurodegenerative diseases, cancer, infectious diseases, and metabolic diseases.
Furthermore, SNPs and mutations in genes encoding proteins involved in autophagy have been implicated in a wide variety of conditions including asthma, Crohn’s disease and cancers.
Popular knockout cell lines for autophagy pathway
Human knockout HAP-1 cells
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Cas9 Stable Cell Lines
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Streamline CRISPR activation experiments with stably expressing dCas9-VPR cell lines
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Top peer reviewed scientific articles using HAP1 cell lines
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