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Image Search Results
Journal: Cell Research
Article Title: Multiplexed activation of endogenous genes by CRISPR-on, an RNA-guided transcriptional activator system
doi: 10.1038/cr.2013.122
Figure Lengend Snippet: dCas9VP160 activates endogenous genes. (A) Protein architecture of dCas9VP160 compared to VP48. (B) Schematic of the human IL1RN promoter region. Locations of transcription start site (TSS) and start codon (ATG) are indicated. Short lines with number indicate targeting sites of the sgRNAs. (C) Activation of human IL1RN expression in HEK293T cells. Cells were analyzed by qRT-PCR 2 days after transfection with dCas9VP160 and the indicated sgRNAs. (D) Schematic of the human SOX2 promoter region. Locations of TSS and start codon (ATG) are indicated. Short lines with number indicate targeting sites of sgRNAs. (E) Activation of SOX2 . Cells were analyzed by qRT-PCR 2 days after transfection with dCas9VP160 and the indicated sgRNAs. (F) Schematic of the human OCT4 promoter region. Locations of transcription start site (TSS) and start codon (ATG) are indicated. Short lines with number indicate targeting sites of sgRNAs. (G) Activation of OCT4 . Cells transfected with dCas9VP160 and the indicated sgRNAs were analyzed by qRT-PCR 2 days later. sgTetO-mut, negative control sgRNA. Error bars show SD among triplicates.
Article Snippet: mESCs from mice carrying a Dox-inducible Musashi-1 (MSI1) allele in the Col1A1 locus were transfected with dCas9VP48 using
Techniques: Activation Assay, Expressing, Quantitative RT-PCR, Transfection, Negative Control
Journal: Cell Research
Article Title: Multiplexed activation of endogenous genes by CRISPR-on, an RNA-guided transcriptional activator system
doi: 10.1038/cr.2013.122
Figure Lengend Snippet: Multiple exogenous and endogenous genes were simultaneously activated by CRISPR-on. (A) One exogenous and two endogenous genes were simultaneously activated by CRISPR-on. Cells were analyzed by qRT-PCR 2 days after transfection with dCas9VP160 and the indicated sgRNAs. (B) Three endogenous genes, SOX2 , IL1RN and OCT4 , can be simultaneously activated by dCas9VP160/sgRNAs. Cells were transfected with dCas9VP160 and the indicated sgRNAs and were analyzed by qRT-PCR 2 days after transfection. The Last three sets of bars represent triple activation experiments using sgSOX2, sgOCT4 and sgIL1RN with three different ratios of sgSOX2:sgIL1RN, keeping the amount of sgOCT4 constant, as indicated by numbers above line. sgTetO-mut, negative control sgRNA. Error bars show SD among triplicates.
Article Snippet: mESCs from mice carrying a Dox-inducible Musashi-1 (MSI1) allele in the Col1A1 locus were transfected with dCas9VP48 using
Techniques: CRISPR, Quantitative RT-PCR, Transfection, Activation Assay, Negative Control