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94
MedChemExpress moz in 3
Moz In 3, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MedChemExpress inhibitor
Inhibitor, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ABclonal Biotechnology anti kat6a
Anti Kat6a, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology anti kat6a
Anti Kat6a, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MedChemExpress reaction buffer
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MedChemExpress anti kat6a
Anti Kat6a, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology moz sirnas
SFK inhibitors and HCK depletion from cells reduces reactivation in experimental and natural latency. a , experimentally latent MoDCs were incubated with medium (DCs), DMSO, or the SFK inhibitors PP2 and PP121 for 3 h and then stimulated with IL-6 and analyzed for IE RNA expression by qRT-PCR 16 h later. b , qRT-PCR for c-fos mRNA expression was performed in unstimulated immature DCs, or immature DCs pretreated with PP2 or a solvent control prior to IL-6 stimulation. c , naturally latent monocytes isolated from two seropositive donors were differentiated in vitro to MoDCs, pretreated with DMSO (−) or PP2 inhibitor (+) for 3 h, and stimulated with IL-6 or lipopolysaccharide ( LPS ) for 16 h, and complementary DNA or RNA (no reverse transcription control) was analyzed using a nested PCR for IE expression. d , HCK RNA expression was analyzed in monocytes, MoDCs, and MoLCs by qRT-PCR. e–g , MoDCs incubated with control or HCK-specific <t>siRNAs</t> were analyzed for HCK RNA expression 48 h after transfection ( e ) or stimulated with IL-6 and analyzed by qRT-PCR for IE ( f ) or cellular ( g ) gene expression 16 h later. *, p < 0.05; **, p < 0.01; NS , not significant.
Moz Sirnas, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/moz/MOZ+siRNA/pmc06721939-172-7-10
Average 90 stars, based on 1 article reviews
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91
Boster Bio mouse anti mof
SFK inhibitors and HCK depletion from cells reduces reactivation in experimental and natural latency. a , experimentally latent MoDCs were incubated with medium (DCs), DMSO, or the SFK inhibitors PP2 and PP121 for 3 h and then stimulated with IL-6 and analyzed for IE RNA expression by qRT-PCR 16 h later. b , qRT-PCR for c-fos mRNA expression was performed in unstimulated immature DCs, or immature DCs pretreated with PP2 or a solvent control prior to IL-6 stimulation. c , naturally latent monocytes isolated from two seropositive donors were differentiated in vitro to MoDCs, pretreated with DMSO (−) or PP2 inhibitor (+) for 3 h, and stimulated with IL-6 or lipopolysaccharide ( LPS ) for 16 h, and complementary DNA or RNA (no reverse transcription control) was analyzed using a nested PCR for IE expression. d , HCK RNA expression was analyzed in monocytes, MoDCs, and MoLCs by qRT-PCR. e–g , MoDCs incubated with control or HCK-specific <t>siRNAs</t> were analyzed for HCK RNA expression 48 h after transfection ( e ) or stimulated with IL-6 and analyzed by qRT-PCR for IE ( f ) or cellular ( g ) gene expression 16 h later. *, p < 0.05; **, p < 0.01; NS , not significant.
Mouse Anti Mof, supplied by Boster Bio, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Promega 35s-labelled moz proteins
SFK inhibitors and HCK depletion from cells reduces reactivation in experimental and natural latency. a , experimentally latent MoDCs were incubated with medium (DCs), DMSO, or the SFK inhibitors PP2 and PP121 for 3 h and then stimulated with IL-6 and analyzed for IE RNA expression by qRT-PCR 16 h later. b , qRT-PCR for c-fos mRNA expression was performed in unstimulated immature DCs, or immature DCs pretreated with PP2 or a solvent control prior to IL-6 stimulation. c , naturally latent monocytes isolated from two seropositive donors were differentiated in vitro to MoDCs, pretreated with DMSO (−) or PP2 inhibitor (+) for 3 h, and stimulated with IL-6 or lipopolysaccharide ( LPS ) for 16 h, and complementary DNA or RNA (no reverse transcription control) was analyzed using a nested PCR for IE expression. d , HCK RNA expression was analyzed in monocytes, MoDCs, and MoLCs by qRT-PCR. e–g , MoDCs incubated with control or HCK-specific <t>siRNAs</t> were analyzed for HCK RNA expression 48 h after transfection ( e ) or stimulated with IL-6 and analyzed by qRT-PCR for IE ( f ) or cellular ( g ) gene expression 16 h later. *, p < 0.05; **, p < 0.01; NS , not significant.
35s Labelled Moz Proteins, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/moz/35s+labelled+moz+proteins/10__1042_slash_bj20061194-88-0-23
Average 90 stars, based on 1 article reviews
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90
Semrush Inc moz seo tools
SFK inhibitors and HCK depletion from cells reduces reactivation in experimental and natural latency. a , experimentally latent MoDCs were incubated with medium (DCs), DMSO, or the SFK inhibitors PP2 and PP121 for 3 h and then stimulated with IL-6 and analyzed for IE RNA expression by qRT-PCR 16 h later. b , qRT-PCR for c-fos mRNA expression was performed in unstimulated immature DCs, or immature DCs pretreated with PP2 or a solvent control prior to IL-6 stimulation. c , naturally latent monocytes isolated from two seropositive donors were differentiated in vitro to MoDCs, pretreated with DMSO (−) or PP2 inhibitor (+) for 3 h, and stimulated with IL-6 or lipopolysaccharide ( LPS ) for 16 h, and complementary DNA or RNA (no reverse transcription control) was analyzed using a nested PCR for IE expression. d , HCK RNA expression was analyzed in monocytes, MoDCs, and MoLCs by qRT-PCR. e–g , MoDCs incubated with control or HCK-specific <t>siRNAs</t> were analyzed for HCK RNA expression 48 h after transfection ( e ) or stimulated with IL-6 and analyzed by qRT-PCR for IE ( f ) or cellular ( g ) gene expression 16 h later. *, p < 0.05; **, p < 0.01; NS , not significant.
Moz Seo Tools, supplied by Semrush Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/moz/moz+seo+tools/10__1007_slash_s10462___024___10780___9-224-25-27
Average 90 stars, based on 1 article reviews
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90
Lebus Corporation märkische oderzeitung—moz
SFK inhibitors and HCK depletion from cells reduces reactivation in experimental and natural latency. a , experimentally latent MoDCs were incubated with medium (DCs), DMSO, or the SFK inhibitors PP2 and PP121 for 3 h and then stimulated with IL-6 and analyzed for IE RNA expression by qRT-PCR 16 h later. b , qRT-PCR for c-fos mRNA expression was performed in unstimulated immature DCs, or immature DCs pretreated with PP2 or a solvent control prior to IL-6 stimulation. c , naturally latent monocytes isolated from two seropositive donors were differentiated in vitro to MoDCs, pretreated with DMSO (−) or PP2 inhibitor (+) for 3 h, and stimulated with IL-6 or lipopolysaccharide ( LPS ) for 16 h, and complementary DNA or RNA (no reverse transcription control) was analyzed using a nested PCR for IE expression. d , HCK RNA expression was analyzed in monocytes, MoDCs, and MoLCs by qRT-PCR. e–g , MoDCs incubated with control or HCK-specific <t>siRNAs</t> were analyzed for HCK RNA expression 48 h after transfection ( e ) or stimulated with IL-6 and analyzed by qRT-PCR for IE ( f ) or cellular ( g ) gene expression 16 h later. *, p < 0.05; **, p < 0.01; NS , not significant.
Märkische Oderzeitung—Moz, supplied by Lebus Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/moz/m%C3%A4rkische+oderzeitung+moz/10__18357_slash_bigr51202421523-581-16-31
Average 90 stars, based on 1 article reviews
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90
GenScript corporation h3(1–19) for moz
SFK inhibitors and HCK depletion from cells reduces reactivation in experimental and natural latency. a , experimentally latent MoDCs were incubated with medium (DCs), DMSO, or the SFK inhibitors PP2 and PP121 for 3 h and then stimulated with IL-6 and analyzed for IE RNA expression by qRT-PCR 16 h later. b , qRT-PCR for c-fos mRNA expression was performed in unstimulated immature DCs, or immature DCs pretreated with PP2 or a solvent control prior to IL-6 stimulation. c , naturally latent monocytes isolated from two seropositive donors were differentiated in vitro to MoDCs, pretreated with DMSO (−) or PP2 inhibitor (+) for 3 h, and stimulated with IL-6 or lipopolysaccharide ( LPS ) for 16 h, and complementary DNA or RNA (no reverse transcription control) was analyzed using a nested PCR for IE expression. d , HCK RNA expression was analyzed in monocytes, MoDCs, and MoLCs by qRT-PCR. e–g , MoDCs incubated with control or HCK-specific <t>siRNAs</t> were analyzed for HCK RNA expression 48 h after transfection ( e ) or stimulated with IL-6 and analyzed by qRT-PCR for IE ( f ) or cellular ( g ) gene expression 16 h later. *, p < 0.05; **, p < 0.01; NS , not significant.
H3(1–19) For Moz, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


SFK inhibitors and HCK depletion from cells reduces reactivation in experimental and natural latency. a , experimentally latent MoDCs were incubated with medium (DCs), DMSO, or the SFK inhibitors PP2 and PP121 for 3 h and then stimulated with IL-6 and analyzed for IE RNA expression by qRT-PCR 16 h later. b , qRT-PCR for c-fos mRNA expression was performed in unstimulated immature DCs, or immature DCs pretreated with PP2 or a solvent control prior to IL-6 stimulation. c , naturally latent monocytes isolated from two seropositive donors were differentiated in vitro to MoDCs, pretreated with DMSO (−) or PP2 inhibitor (+) for 3 h, and stimulated with IL-6 or lipopolysaccharide ( LPS ) for 16 h, and complementary DNA or RNA (no reverse transcription control) was analyzed using a nested PCR for IE expression. d , HCK RNA expression was analyzed in monocytes, MoDCs, and MoLCs by qRT-PCR. e–g , MoDCs incubated with control or HCK-specific siRNAs were analyzed for HCK RNA expression 48 h after transfection ( e ) or stimulated with IL-6 and analyzed by qRT-PCR for IE ( f ) or cellular ( g ) gene expression 16 h later. *, p < 0.05; **, p < 0.01; NS , not significant.

Journal: The Journal of Biological Chemistry

Article Title: Src family kinase activity drives cytomegalovirus reactivation by recruiting MOZ histone acetyltransferase activity to the viral promoter

doi: 10.1074/jbc.RA119.009667

Figure Lengend Snippet: SFK inhibitors and HCK depletion from cells reduces reactivation in experimental and natural latency. a , experimentally latent MoDCs were incubated with medium (DCs), DMSO, or the SFK inhibitors PP2 and PP121 for 3 h and then stimulated with IL-6 and analyzed for IE RNA expression by qRT-PCR 16 h later. b , qRT-PCR for c-fos mRNA expression was performed in unstimulated immature DCs, or immature DCs pretreated with PP2 or a solvent control prior to IL-6 stimulation. c , naturally latent monocytes isolated from two seropositive donors were differentiated in vitro to MoDCs, pretreated with DMSO (−) or PP2 inhibitor (+) for 3 h, and stimulated with IL-6 or lipopolysaccharide ( LPS ) for 16 h, and complementary DNA or RNA (no reverse transcription control) was analyzed using a nested PCR for IE expression. d , HCK RNA expression was analyzed in monocytes, MoDCs, and MoLCs by qRT-PCR. e–g , MoDCs incubated with control or HCK-specific siRNAs were analyzed for HCK RNA expression 48 h after transfection ( e ) or stimulated with IL-6 and analyzed by qRT-PCR for IE ( f ) or cellular ( g ) gene expression 16 h later. *, p < 0.05; **, p < 0.01; NS , not significant.

Article Snippet: Pooled HCK siRNAs (Hck 4392420, Ambion) or MOZ siRNAs (sc-37959, Santa Cruz Biotechnology) were transfected into DCs and then knockdown was confirmed 48 h after transfection using gene-specific primers.

Techniques: Incubation, RNA Expression, Quantitative RT-PCR, Expressing, Solvent, Control, Isolation, In Vitro, Reverse Transcription, Nested PCR, Transfection, Gene Expression

HCMV reactivation depends on MOZ histone acetyltransferase activity. a and b , experimentally latent MoDCs were incubated with medium (DCs), DMSO, or inhibitors of p300, Tip60/MOZ (MG149, 75 μ m ), or MOZ (MG149, 25 μ m ) for 3 h and then stimulated with IL-6 and analyzed for IE ( a ) and UL44 ( b ) RNA expression by qRT-PCR 16 h later. c , Western blot for MoDCs treated with histone H3 ( H3 ) or histone H3 acetylation on lysine 14 ( H3K14Ac ) in DMSO ( C ), CPTH2 ( CP ), and NU9056 ( Nu ). d and e , MoDCs incubated with control or MOZ-specific siRNAs were analyzed for MOZ RNA expression 48 h after transfection ( d ) or subsequently stimulated with IL-6 and analyzed by qRT-PCR for IE ( e ) and UL144 gene expression 16 h later. *, p < 0.05; **, p < 0.01; NS , not significant.

Journal: The Journal of Biological Chemistry

Article Title: Src family kinase activity drives cytomegalovirus reactivation by recruiting MOZ histone acetyltransferase activity to the viral promoter

doi: 10.1074/jbc.RA119.009667

Figure Lengend Snippet: HCMV reactivation depends on MOZ histone acetyltransferase activity. a and b , experimentally latent MoDCs were incubated with medium (DCs), DMSO, or inhibitors of p300, Tip60/MOZ (MG149, 75 μ m ), or MOZ (MG149, 25 μ m ) for 3 h and then stimulated with IL-6 and analyzed for IE ( a ) and UL44 ( b ) RNA expression by qRT-PCR 16 h later. c , Western blot for MoDCs treated with histone H3 ( H3 ) or histone H3 acetylation on lysine 14 ( H3K14Ac ) in DMSO ( C ), CPTH2 ( CP ), and NU9056 ( Nu ). d and e , MoDCs incubated with control or MOZ-specific siRNAs were analyzed for MOZ RNA expression 48 h after transfection ( d ) or subsequently stimulated with IL-6 and analyzed by qRT-PCR for IE ( e ) and UL144 gene expression 16 h later. *, p < 0.05; **, p < 0.01; NS , not significant.

Article Snippet: Pooled HCK siRNAs (Hck 4392420, Ambion) or MOZ siRNAs (sc-37959, Santa Cruz Biotechnology) were transfected into DCs and then knockdown was confirmed 48 h after transfection using gene-specific primers.

Techniques: Activity Assay, Incubation, RNA Expression, Quantitative RT-PCR, Western Blot, Control, Transfection, Gene Expression