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Addgene inc plasmid
Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/u6+sgrna/AAV-U6-sgRNA-hSyn-mCherry+(Plasmid+%2387916)/pm42906853-47-12-18
Average 93 stars, based on 19 article reviews
plasmid - by Bioz Stars, 2026-10
93/100 stars

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Related Articles

Cloning:

Article Title: Optimizing CRISPR/Cas9 approaches in the polymorphic tunicate Ciona intestinalis.
Article Snippet: Briefly, oligo pairs were phosphorylated and annealed using the T4 polynucleotide kinase (NEB, Cat#: M0201). .. The obtained reaction was used for cloning into the U6>sgRNA (F + E) vector (obtained from Addgene) in a one-step Golden Gate assembly reaction. .. The plasmid was transformed into JM109 chemically competent bacteria (Promega, Cat#: L2005).

Article Title: Multiple pathways for glucose phosphate transport and utilization support growth of Cryptosporidium parvum.
Article Snippet: .. CRISPR/Cas9 plasmids were generated by adding a sgRNA targeting the gene of interest into the linear Cas9 plasmid that was amplified from pACT:Cas9-GFP, U6:sgRNA (addgene plasmid no. 128552) via Gibson assembly cloning. ..

Plasmid Preparation:

Article Title: Optimizing CRISPR/Cas9 approaches in the polymorphic tunicate Ciona intestinalis.
Article Snippet: Briefly, oligo pairs were phosphorylated and annealed using the T4 polynucleotide kinase (NEB, Cat#: M0201). .. The obtained reaction was used for cloning into the U6>sgRNA (F + E) vector (obtained from Addgene) in a one-step Golden Gate assembly reaction. .. The plasmid was transformed into JM109 chemically competent bacteria (Promega, Cat#: L2005).

Article Title: In vivo human T cell engineering with enveloped delivery vehicles.
Article Snippet: .. In brief, VSVG-pseudotyped Cas9-EDVs were produced by seeding 3.5–4 million Lenti-X cells (Takara Bio) into 10 cm tissue culture dishes (Corning) and transfecting the next day with 1 μg pCMV-VSV-G (Addgene plasmid no. 8454), 6.7 μg Gag-Cas9 (Addgene plasmid no. 171060), 3.3 μg psPax2 (Addgene plasmid no. 12260) and 10 μg U6-sgRNA (Addgene plasmid no. 171635 or Addgene plasmid no. 171634) using polyethylenimine (Polysciences) at a 3:1 PEI:plasmid ratio. ..

Article Title: Multiple pathways for glucose phosphate transport and utilization support growth of Cryptosporidium parvum.
Article Snippet: .. CRISPR/Cas9 plasmids were generated by adding a sgRNA targeting the gene of interest into the linear Cas9 plasmid that was amplified from pACT:Cas9-GFP, U6:sgRNA (addgene plasmid no. 128552) via Gibson assembly cloning. ..

Article Title: Establishment of human expanded potential stem cell lines via preimplantation embryo cultivation and somatic cell reprogramming.
Article Snippet: We previously reported the derivation of expanded potential stem cells (EPSCs) by modulating signaling pathways involved in preimplantation embryogenesis.. These cells exhibit expanded developmental potential into embryonic and extraembryonic lineages, and we have shown that human EPSCs (hEPSCs) possess trophoblast differentiation potency for generating human trophoblast stem cells.. Here we report protocols for deriving stable hEPSC lines directly from morula or early blastocyst stages of human preimplantation embryos (hEPSC-em) and by reprogramming human dermal fibroblasts (human induced EPSCs) using six exogenous factors, as an extension to our previous protocols on deriving porcine EPSCs from preimplantation embryos and by reprogramming somatic cells.

Produced:

Article Title: In vivo human T cell engineering with enveloped delivery vehicles.
Article Snippet: .. In brief, VSVG-pseudotyped Cas9-EDVs were produced by seeding 3.5–4 million Lenti-X cells (Takara Bio) into 10 cm tissue culture dishes (Corning) and transfecting the next day with 1 μg pCMV-VSV-G (Addgene plasmid no. 8454), 6.7 μg Gag-Cas9 (Addgene plasmid no. 171060), 3.3 μg psPax2 (Addgene plasmid no. 12260) and 10 μg U6-sgRNA (Addgene plasmid no. 171635 or Addgene plasmid no. 171634) using polyethylenimine (Polysciences) at a 3:1 PEI:plasmid ratio. ..

other:

Article Title: Descending locus coeruleus noradrenergic signaling to spinal astrocyte subset is required for stress-induced mechanical pain hypersensitivity
Article Snippet: The genes encoding GCaMP6m (#40754; Addgene), Cre, GRAB NE1m (#123308; Addgene) and mCherry were subcloned into the pENTR plasmid (Thermo Fisher Scientific).

Article Title: Descending locus coeruleus noradrenergic signaling to spinal astrocyte subset is required for stress-induced mechanical pain hypersensitivity
Article Snippet: The genes encoding GCaMP6m (#40754; Addgene), Cre, GRABNE1m (#123308; Addgene) and mCherry were subcloned into the pENTR plasmid (Thermo Fisher Scientific).

Article Title: Descending locus coeruleus noradrenergic signaling to spinal astrocyte subset is required for stress-induced pain facilitation
Article Snippet: To produce the AAV vector for the Cre-switch system, vectors containing the promoters encoding EF1α were generated from pAAV-CA-FLEX (#38042; Addgene) by substituting the promoter.

CRISPR:

Article Title: Multiple pathways for glucose phosphate transport and utilization support growth of Cryptosporidium parvum.
Article Snippet: .. CRISPR/Cas9 plasmids were generated by adding a sgRNA targeting the gene of interest into the linear Cas9 plasmid that was amplified from pACT:Cas9-GFP, U6:sgRNA (addgene plasmid no. 128552) via Gibson assembly cloning. ..

Generated:

Article Title: Multiple pathways for glucose phosphate transport and utilization support growth of Cryptosporidium parvum.
Article Snippet: .. CRISPR/Cas9 plasmids were generated by adding a sgRNA targeting the gene of interest into the linear Cas9 plasmid that was amplified from pACT:Cas9-GFP, U6:sgRNA (addgene plasmid no. 128552) via Gibson assembly cloning. ..

Article Title: Establishment of human expanded potential stem cell lines via preimplantation embryo cultivation and somatic cell reprogramming.
Article Snippet: We previously reported the derivation of expanded potential stem cells (EPSCs) by modulating signaling pathways involved in preimplantation embryogenesis.. These cells exhibit expanded developmental potential into embryonic and extraembryonic lineages, and we have shown that human EPSCs (hEPSCs) possess trophoblast differentiation potency for generating human trophoblast stem cells.. Here we report protocols for deriving stable hEPSC lines directly from morula or early blastocyst stages of human preimplantation embryos (hEPSC-em) and by reprogramming human dermal fibroblasts (human induced EPSCs) using six exogenous factors, as an extension to our previous protocols on deriving porcine EPSCs from preimplantation embryos and by reprogramming somatic cells.

Amplification:

Article Title: Multiple pathways for glucose phosphate transport and utilization support growth of Cryptosporidium parvum.
Article Snippet: .. CRISPR/Cas9 plasmids were generated by adding a sgRNA targeting the gene of interest into the linear Cas9 plasmid that was amplified from pACT:Cas9-GFP, U6:sgRNA (addgene plasmid no. 128552) via Gibson assembly cloning. ..



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a, Gene structure of <t>MAF</t> and <t>MAFB</t> indicating position of CRISPR/Cas9 target sites in the 5’ and 3’ UTR of both genes, and indels obtained. The first line of each sequence block refers to the wild-type locus, subsequent lines indicate the indels generated by CRISPR/Cas9 editing. Start and stop codons are bold, genomic target sequences are underlined. The protospacer positions are shown as a black line close to the start or stop codon. b, gene expression of MAF (black) or MAFB (white) by qPCR. c, Protein expression of MAF and MAFB by immunoblotting. d, Schematic of human iPSC-derived macrophage differentiation indicating timing and cytokines e, GSEA of MYC and E2F targets. f, Phase-contrast images from single cell cultures of EB harvest-derived WT macrophages at indicated time points. g, Schematic of an oxygen consumption rate (OCR) profile from a Seahorse MitoStress test assay. Indicated are readout parameters including basal respiration (Basal), ATP production (ATP), maximum respiration (Maximum), spare respiratory capacity (Spare), and non-mitochondrial respiration (orange), as well as administration of oligomycin, Carbonyl cyanide-4-(trifluoromethoxy)-phenylhydrazone (FCCP), and rotenone/Antimycin A (Rot/AMA). h-j, Quantification of ATP production ( h ), maximum respiration ( i ), and basal respiration ( j ) from Seahorse analysis of unstimulated MAF-DKO or WT macrophages. k, Flow cytometric quantification of HLA-DR surface expression by MFI. Statistical analysis was performed using unpaired two-tailed t-tests. Data shown as mean ± s.d. Representative results from one of at least three independent experiments. Full gene set descriptions shown in Extended Data Table 4. EB, embryoid body.
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a, Gene structure of <t>MAF</t> and <t>MAFB</t> indicating position of CRISPR/Cas9 target sites in the 5’ and 3’ UTR of both genes, and indels obtained. The first line of each sequence block refers to the wild-type locus, subsequent lines indicate the indels generated by CRISPR/Cas9 editing. Start and stop codons are bold, genomic target sequences are underlined. The protospacer positions are shown as a black line close to the start or stop codon. b, gene expression of MAF (black) or MAFB (white) by qPCR. c, Protein expression of MAF and MAFB by immunoblotting. d, Schematic of human iPSC-derived macrophage differentiation indicating timing and cytokines e, GSEA of MYC and E2F targets. f, Phase-contrast images from single cell cultures of EB harvest-derived WT macrophages at indicated time points. g, Schematic of an oxygen consumption rate (OCR) profile from a Seahorse MitoStress test assay. Indicated are readout parameters including basal respiration (Basal), ATP production (ATP), maximum respiration (Maximum), spare respiratory capacity (Spare), and non-mitochondrial respiration (orange), as well as administration of oligomycin, Carbonyl cyanide-4-(trifluoromethoxy)-phenylhydrazone (FCCP), and rotenone/Antimycin A (Rot/AMA). h-j, Quantification of ATP production ( h ), maximum respiration ( i ), and basal respiration ( j ) from Seahorse analysis of unstimulated MAF-DKO or WT macrophages. k, Flow cytometric quantification of HLA-DR surface expression by MFI. Statistical analysis was performed using unpaired two-tailed t-tests. Data shown as mean ± s.d. Representative results from one of at least three independent experiments. Full gene set descriptions shown in Extended Data Table 4. EB, embryoid body.
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a, Gene structure of <t>MAF</t> and <t>MAFB</t> indicating position of CRISPR/Cas9 target sites in the 5’ and 3’ UTR of both genes, and indels obtained. The first line of each sequence block refers to the wild-type locus, subsequent lines indicate the indels generated by CRISPR/Cas9 editing. Start and stop codons are bold, genomic target sequences are underlined. The protospacer positions are shown as a black line close to the start or stop codon. b, gene expression of MAF (black) or MAFB (white) by qPCR. c, Protein expression of MAF and MAFB by immunoblotting. d, Schematic of human iPSC-derived macrophage differentiation indicating timing and cytokines e, GSEA of MYC and E2F targets. f, Phase-contrast images from single cell cultures of EB harvest-derived WT macrophages at indicated time points. g, Schematic of an oxygen consumption rate (OCR) profile from a Seahorse MitoStress test assay. Indicated are readout parameters including basal respiration (Basal), ATP production (ATP), maximum respiration (Maximum), spare respiratory capacity (Spare), and non-mitochondrial respiration (orange), as well as administration of oligomycin, Carbonyl cyanide-4-(trifluoromethoxy)-phenylhydrazone (FCCP), and rotenone/Antimycin A (Rot/AMA). h-j, Quantification of ATP production ( h ), maximum respiration ( i ), and basal respiration ( j ) from Seahorse analysis of unstimulated MAF-DKO or WT macrophages. k, Flow cytometric quantification of HLA-DR surface expression by MFI. Statistical analysis was performed using unpaired two-tailed t-tests. Data shown as mean ± s.d. Representative results from one of at least three independent experiments. Full gene set descriptions shown in Extended Data Table 4. EB, embryoid body.
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a, Gene structure of <t>MAF</t> and <t>MAFB</t> indicating position of CRISPR/Cas9 target sites in the 5’ and 3’ UTR of both genes, and indels obtained. The first line of each sequence block refers to the wild-type locus, subsequent lines indicate the indels generated by CRISPR/Cas9 editing. Start and stop codons are bold, genomic target sequences are underlined. The protospacer positions are shown as a black line close to the start or stop codon. b, gene expression of MAF (black) or MAFB (white) by qPCR. c, Protein expression of MAF and MAFB by immunoblotting. d, Schematic of human iPSC-derived macrophage differentiation indicating timing and cytokines e, GSEA of MYC and E2F targets. f, Phase-contrast images from single cell cultures of EB harvest-derived WT macrophages at indicated time points. g, Schematic of an oxygen consumption rate (OCR) profile from a Seahorse MitoStress test assay. Indicated are readout parameters including basal respiration (Basal), ATP production (ATP), maximum respiration (Maximum), spare respiratory capacity (Spare), and non-mitochondrial respiration (orange), as well as administration of oligomycin, Carbonyl cyanide-4-(trifluoromethoxy)-phenylhydrazone (FCCP), and rotenone/Antimycin A (Rot/AMA). h-j, Quantification of ATP production ( h ), maximum respiration ( i ), and basal respiration ( j ) from Seahorse analysis of unstimulated MAF-DKO or WT macrophages. k, Flow cytometric quantification of HLA-DR surface expression by MFI. Statistical analysis was performed using unpaired two-tailed t-tests. Data shown as mean ± s.d. Representative results from one of at least three independent experiments. Full gene set descriptions shown in Extended Data Table 4. EB, embryoid body.
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a, Gene structure of <t>MAF</t> and <t>MAFB</t> indicating position of CRISPR/Cas9 target sites in the 5’ and 3’ UTR of both genes, and indels obtained. The first line of each sequence block refers to the wild-type locus, subsequent lines indicate the indels generated by CRISPR/Cas9 editing. Start and stop codons are bold, genomic target sequences are underlined. The protospacer positions are shown as a black line close to the start or stop codon. b, gene expression of MAF (black) or MAFB (white) by qPCR. c, Protein expression of MAF and MAFB by immunoblotting. d, Schematic of human iPSC-derived macrophage differentiation indicating timing and cytokines e, GSEA of MYC and E2F targets. f, Phase-contrast images from single cell cultures of EB harvest-derived WT macrophages at indicated time points. g, Schematic of an oxygen consumption rate (OCR) profile from a Seahorse MitoStress test assay. Indicated are readout parameters including basal respiration (Basal), ATP production (ATP), maximum respiration (Maximum), spare respiratory capacity (Spare), and non-mitochondrial respiration (orange), as well as administration of oligomycin, Carbonyl cyanide-4-(trifluoromethoxy)-phenylhydrazone (FCCP), and rotenone/Antimycin A (Rot/AMA). h-j, Quantification of ATP production ( h ), maximum respiration ( i ), and basal respiration ( j ) from Seahorse analysis of unstimulated MAF-DKO or WT macrophages. k, Flow cytometric quantification of HLA-DR surface expression by MFI. Statistical analysis was performed using unpaired two-tailed t-tests. Data shown as mean ± s.d. Representative results from one of at least three independent experiments. Full gene set descriptions shown in Extended Data Table 4. EB, embryoid body.
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a, Gene structure of <t>MAF</t> and <t>MAFB</t> indicating position of CRISPR/Cas9 target sites in the 5’ and 3’ UTR of both genes, and indels obtained. The first line of each sequence block refers to the wild-type locus, subsequent lines indicate the indels generated by CRISPR/Cas9 editing. Start and stop codons are bold, genomic target sequences are underlined. The protospacer positions are shown as a black line close to the start or stop codon. b, gene expression of MAF (black) or MAFB (white) by qPCR. c, Protein expression of MAF and MAFB by immunoblotting. d, Schematic of human iPSC-derived macrophage differentiation indicating timing and cytokines e, GSEA of MYC and E2F targets. f, Phase-contrast images from single cell cultures of EB harvest-derived WT macrophages at indicated time points. g, Schematic of an oxygen consumption rate (OCR) profile from a Seahorse MitoStress test assay. Indicated are readout parameters including basal respiration (Basal), ATP production (ATP), maximum respiration (Maximum), spare respiratory capacity (Spare), and non-mitochondrial respiration (orange), as well as administration of oligomycin, Carbonyl cyanide-4-(trifluoromethoxy)-phenylhydrazone (FCCP), and rotenone/Antimycin A (Rot/AMA). h-j, Quantification of ATP production ( h ), maximum respiration ( i ), and basal respiration ( j ) from Seahorse analysis of unstimulated MAF-DKO or WT macrophages. k, Flow cytometric quantification of HLA-DR surface expression by MFI. Statistical analysis was performed using unpaired two-tailed t-tests. Data shown as mean ± s.d. Representative results from one of at least three independent experiments. Full gene set descriptions shown in Extended Data Table 4. EB, embryoid body.
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Image Search Results


a, Gene structure of MAF and MAFB indicating position of CRISPR/Cas9 target sites in the 5’ and 3’ UTR of both genes, and indels obtained. The first line of each sequence block refers to the wild-type locus, subsequent lines indicate the indels generated by CRISPR/Cas9 editing. Start and stop codons are bold, genomic target sequences are underlined. The protospacer positions are shown as a black line close to the start or stop codon. b, gene expression of MAF (black) or MAFB (white) by qPCR. c, Protein expression of MAF and MAFB by immunoblotting. d, Schematic of human iPSC-derived macrophage differentiation indicating timing and cytokines e, GSEA of MYC and E2F targets. f, Phase-contrast images from single cell cultures of EB harvest-derived WT macrophages at indicated time points. g, Schematic of an oxygen consumption rate (OCR) profile from a Seahorse MitoStress test assay. Indicated are readout parameters including basal respiration (Basal), ATP production (ATP), maximum respiration (Maximum), spare respiratory capacity (Spare), and non-mitochondrial respiration (orange), as well as administration of oligomycin, Carbonyl cyanide-4-(trifluoromethoxy)-phenylhydrazone (FCCP), and rotenone/Antimycin A (Rot/AMA). h-j, Quantification of ATP production ( h ), maximum respiration ( i ), and basal respiration ( j ) from Seahorse analysis of unstimulated MAF-DKO or WT macrophages. k, Flow cytometric quantification of HLA-DR surface expression by MFI. Statistical analysis was performed using unpaired two-tailed t-tests. Data shown as mean ± s.d. Representative results from one of at least three independent experiments. Full gene set descriptions shown in Extended Data Table 4. EB, embryoid body.

Journal: bioRxiv

Article Title: Stemness overcomes IFNγ-induced antitumour exhaustion in human macrophages

doi: 10.64898/2026.10.06.756629

Figure Lengend Snippet: a, Gene structure of MAF and MAFB indicating position of CRISPR/Cas9 target sites in the 5’ and 3’ UTR of both genes, and indels obtained. The first line of each sequence block refers to the wild-type locus, subsequent lines indicate the indels generated by CRISPR/Cas9 editing. Start and stop codons are bold, genomic target sequences are underlined. The protospacer positions are shown as a black line close to the start or stop codon. b, gene expression of MAF (black) or MAFB (white) by qPCR. c, Protein expression of MAF and MAFB by immunoblotting. d, Schematic of human iPSC-derived macrophage differentiation indicating timing and cytokines e, GSEA of MYC and E2F targets. f, Phase-contrast images from single cell cultures of EB harvest-derived WT macrophages at indicated time points. g, Schematic of an oxygen consumption rate (OCR) profile from a Seahorse MitoStress test assay. Indicated are readout parameters including basal respiration (Basal), ATP production (ATP), maximum respiration (Maximum), spare respiratory capacity (Spare), and non-mitochondrial respiration (orange), as well as administration of oligomycin, Carbonyl cyanide-4-(trifluoromethoxy)-phenylhydrazone (FCCP), and rotenone/Antimycin A (Rot/AMA). h-j, Quantification of ATP production ( h ), maximum respiration ( i ), and basal respiration ( j ) from Seahorse analysis of unstimulated MAF-DKO or WT macrophages. k, Flow cytometric quantification of HLA-DR surface expression by MFI. Statistical analysis was performed using unpaired two-tailed t-tests. Data shown as mean ± s.d. Representative results from one of at least three independent experiments. Full gene set descriptions shown in Extended Data Table 4. EB, embryoid body.

Article Snippet: In brief, BIHi001-A-1 were exposed to sgRNA-expressing plasmids targeting MAF and MAFB (pU6-(BbsI)sgRNA_CAG-venus-bpA, 86985, Addgene).

Techniques: CRISPR, Sequencing, Blocking Assay, Generated, Gene Expression, Expressing, Western Blot, Derivative Assay, Phase Contrast, Single Cell, Analysis, Two Tailed Test, IPSC

a,b UMAP projections of scRNAseq showing genotype and treatment conditions ( a ) and IFNγ-induced genes ( b ) in WT and MAF-DKO macrophages before and after stimulation with IFNγ followed by TCM. c, proportional Venn diagrams showing differential IFNγ-induced genes of WT and MAF-DKO macrophages in response to IFNγ and TCM. d, Heatmap of top100 IFNγ-induced DEGs for each genotype. e, Violin plots showing gene signature scores for ISG monocytes (ISG monos) and IL4I1 + TAMs (IL4I1 TAMs) in WT and MAF-DKO macrophages. f, Violin plots showing z-score expression of selected genes from ( d ). g, GSEA of IL6 and IL10 pathway gene sets in IFNγ-stimulated WT and MAF-DKO macrophages. h, Quantification of cytokine concentrations in supernatants of IFNγ-stimulated WT and MAF-DKO macrophages, n = 3 per group. i, Radar plot showing z-score of selected TF regulon activity in WT and MAF-DKO macrophages after IFNγ. j,k, UMAP projections and quantifications of selected surface marker expression in WT and MAF-DKO macrophages by spectral flow cytometry, n = 3 per group. l, Quantification of intracellular ROS levels in IFNγ-stimulated WT and MAF-DKO macrophages, monitored by DHR fluorescence signal in Incucyte SX5 live-cell imaging, expressed as relative green fluorescence per well normalised to cell confluence, n = 3 per group. m, Violin plots showing MAFB expression in WT macrophages in indicated conditions. Statistical analysis was performed using an unpaired twotailed t -tests ( e,f,h,k ), mixed-effect analysis (RELM model) ( l ) or two-way ANOVA with Tukey’s post hoc t test ( m ). Data shown as mean ± s.d. and representative of at least three independent experiments ( e,f,h,j,k,l,m ). Full gene set descriptions shown in Extended Data Table 4. TF, transcription factor. TCM, tumour cell conditioned medium. DHR, dihydrorhodamine 123. ROS, reactive oxygen species.

Journal: bioRxiv

Article Title: Stemness overcomes IFNγ-induced antitumour exhaustion in human macrophages

doi: 10.64898/2026.10.06.756629

Figure Lengend Snippet: a,b UMAP projections of scRNAseq showing genotype and treatment conditions ( a ) and IFNγ-induced genes ( b ) in WT and MAF-DKO macrophages before and after stimulation with IFNγ followed by TCM. c, proportional Venn diagrams showing differential IFNγ-induced genes of WT and MAF-DKO macrophages in response to IFNγ and TCM. d, Heatmap of top100 IFNγ-induced DEGs for each genotype. e, Violin plots showing gene signature scores for ISG monocytes (ISG monos) and IL4I1 + TAMs (IL4I1 TAMs) in WT and MAF-DKO macrophages. f, Violin plots showing z-score expression of selected genes from ( d ). g, GSEA of IL6 and IL10 pathway gene sets in IFNγ-stimulated WT and MAF-DKO macrophages. h, Quantification of cytokine concentrations in supernatants of IFNγ-stimulated WT and MAF-DKO macrophages, n = 3 per group. i, Radar plot showing z-score of selected TF regulon activity in WT and MAF-DKO macrophages after IFNγ. j,k, UMAP projections and quantifications of selected surface marker expression in WT and MAF-DKO macrophages by spectral flow cytometry, n = 3 per group. l, Quantification of intracellular ROS levels in IFNγ-stimulated WT and MAF-DKO macrophages, monitored by DHR fluorescence signal in Incucyte SX5 live-cell imaging, expressed as relative green fluorescence per well normalised to cell confluence, n = 3 per group. m, Violin plots showing MAFB expression in WT macrophages in indicated conditions. Statistical analysis was performed using an unpaired twotailed t -tests ( e,f,h,k ), mixed-effect analysis (RELM model) ( l ) or two-way ANOVA with Tukey’s post hoc t test ( m ). Data shown as mean ± s.d. and representative of at least three independent experiments ( e,f,h,j,k,l,m ). Full gene set descriptions shown in Extended Data Table 4. TF, transcription factor. TCM, tumour cell conditioned medium. DHR, dihydrorhodamine 123. ROS, reactive oxygen species.

Article Snippet: In brief, BIHi001-A-1 were exposed to sgRNA-expressing plasmids targeting MAF and MAFB (pU6-(BbsI)sgRNA_CAG-venus-bpA, 86985, Addgene).

Techniques: Expressing, Activity Assay, Marker, Flow Cytometry, Fluorescence, Live Cell Imaging, Analysis