c jun  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc c jun
    C Jun, supplied by Cell Signaling Technology Inc, 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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    c jun sirna  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc c jun sirna
    Densities of bands were quantified by Eagle Eye II software. GAPDH levels, measured in parallel, served as controls. Arsenite-transformed HELF cells were transfected with 50 nM of control <t>siRNA,</t> <t>NF-κB</t> <t>p65</t> siRNA, or c-Jun siRNA for 24 h. (A) Western blots and (B) relative protein levels (means ± SD, n = 3) of NF-κB p65 and c-Jun. (C) qRT-PCR analysis of miR-21 expression (means ± SD, n = 3). ** P <0.01 difference from Con siRNA group. (D) Western blots (upper) and RT-PCR (below) analyses for protein and mRNA levels and (E) relative protein levels (means ± SD, n = 3) of Pdcd4, Spry1, cleaved-caspase-3, and caspase-3, ** P <0.01 difference from the control (Con) siRNA group.
    C Jun Sirna, supplied by Cell Signaling Technology Inc, 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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    1) Product Images from "Feedback Regulations of miR-21 and MAPKs via Pdcd4 and Spry1 Are Involved in Arsenite-Induced Cell Malignant Transformation"

    Article Title: Feedback Regulations of miR-21 and MAPKs via Pdcd4 and Spry1 Are Involved in Arsenite-Induced Cell Malignant Transformation

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0057652

    Densities of bands were quantified by Eagle Eye II software. GAPDH levels, measured in parallel, served as controls. Arsenite-transformed HELF cells were transfected with 50 nM of control siRNA, NF-κB p65 siRNA, or c-Jun siRNA for 24 h. (A) Western blots and (B) relative protein levels (means ± SD, n = 3) of NF-κB p65 and c-Jun. (C) qRT-PCR analysis of miR-21 expression (means ± SD, n = 3). ** P <0.01 difference from Con siRNA group. (D) Western blots (upper) and RT-PCR (below) analyses for protein and mRNA levels and (E) relative protein levels (means ± SD, n = 3) of Pdcd4, Spry1, cleaved-caspase-3, and caspase-3, ** P <0.01 difference from the control (Con) siRNA group.
    Figure Legend Snippet: Densities of bands were quantified by Eagle Eye II software. GAPDH levels, measured in parallel, served as controls. Arsenite-transformed HELF cells were transfected with 50 nM of control siRNA, NF-κB p65 siRNA, or c-Jun siRNA for 24 h. (A) Western blots and (B) relative protein levels (means ± SD, n = 3) of NF-κB p65 and c-Jun. (C) qRT-PCR analysis of miR-21 expression (means ± SD, n = 3). ** P <0.01 difference from Con siRNA group. (D) Western blots (upper) and RT-PCR (below) analyses for protein and mRNA levels and (E) relative protein levels (means ± SD, n = 3) of Pdcd4, Spry1, cleaved-caspase-3, and caspase-3, ** P <0.01 difference from the control (Con) siRNA group.

    Techniques Used: Software, Transformation Assay, Transfection, Western Blot, Quantitative RT-PCR, Expressing, Reverse Transcription Polymerase Chain Reaction

    c jun sirna  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc c jun sirna
    Knockdown efficiency of c-Jun <t>and</t> <t>CREB</t> mRNA and IL-32 expression induced by IFNγ and H 2 O 2 in HBE cells transfected with c-Jun or CREB siRNAs . c-Jun (A) and CREB (B) mRNA expression levels examined by quantitative real time PCR in HBE cells transfected with indicated siRNAs. Expression levels of c-Jun (A) and CREB (B) by each <t>siRNA</t> transfection were looked by quantitative real time PCR. IL-32 expression was examined by real time PCR in HBE cells transfected with control-siRNA, closed bars, c-Jun-siRNA, open bars, or CREB-siRNA, hatched bars, respectively. Then 48 hours after transfection, cells were stimulated with H 2 O 2 and/or IFNγ, followed by IL-32 quantitative real time PCR of RNA extracted 24 hours after the stimulation (C). The bars represent the means ± SE from 3 different individuals. *p < 0.05 significantly different.
    C Jun Sirna, supplied by Cell Signaling Technology Inc, 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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    1) Product Images from "Oxidative stress induced Interleukin-32 mRNA expression in human bronchial epithelial cells"

    Article Title: Oxidative stress induced Interleukin-32 mRNA expression in human bronchial epithelial cells

    Journal: Respiratory Research

    doi: 10.1186/1465-9921-13-19

    Knockdown efficiency of c-Jun and CREB mRNA and IL-32 expression induced by IFNγ and H 2 O 2 in HBE cells transfected with c-Jun or CREB siRNAs . c-Jun (A) and CREB (B) mRNA expression levels examined by quantitative real time PCR in HBE cells transfected with indicated siRNAs. Expression levels of c-Jun (A) and CREB (B) by each siRNA transfection were looked by quantitative real time PCR. IL-32 expression was examined by real time PCR in HBE cells transfected with control-siRNA, closed bars, c-Jun-siRNA, open bars, or CREB-siRNA, hatched bars, respectively. Then 48 hours after transfection, cells were stimulated with H 2 O 2 and/or IFNγ, followed by IL-32 quantitative real time PCR of RNA extracted 24 hours after the stimulation (C). The bars represent the means ± SE from 3 different individuals. *p < 0.05 significantly different.
    Figure Legend Snippet: Knockdown efficiency of c-Jun and CREB mRNA and IL-32 expression induced by IFNγ and H 2 O 2 in HBE cells transfected with c-Jun or CREB siRNAs . c-Jun (A) and CREB (B) mRNA expression levels examined by quantitative real time PCR in HBE cells transfected with indicated siRNAs. Expression levels of c-Jun (A) and CREB (B) by each siRNA transfection were looked by quantitative real time PCR. IL-32 expression was examined by real time PCR in HBE cells transfected with control-siRNA, closed bars, c-Jun-siRNA, open bars, or CREB-siRNA, hatched bars, respectively. Then 48 hours after transfection, cells were stimulated with H 2 O 2 and/or IFNγ, followed by IL-32 quantitative real time PCR of RNA extracted 24 hours after the stimulation (C). The bars represent the means ± SE from 3 different individuals. *p < 0.05 significantly different.

    Techniques Used: Expressing, Transfection, Real-time Polymerase Chain Reaction

    c jun  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc c jun
    C Jun, supplied by Cell Signaling Technology Inc, 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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    sirna c jun  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc sirna c jun
    (A) Western blotting analysis showing transfection efficiency of siRNA c-jun in both PC-3 and LNCaP cells. (B) Cell proliferation in LNCaP (upper panel) and PC-3 (lower panel) cells transfected with c-jun siRNA or nontargeted (control) vector. Cells were treated with Doc for 24 and 48 hours. LNCaP cells harbor c-jun siRNA showed a significant decrease in proliferation (p=0.002) while PC-3 cells were not affected.
    Sirna C Jun, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Interaction between c-jun and Androgen Receptor Determines the Outcome of Taxane Therapy in Castration Resistant Prostate Cancer"

    Article Title: Interaction between c-jun and Androgen Receptor Determines the Outcome of Taxane Therapy in Castration Resistant Prostate Cancer

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0079573

    (A) Western blotting analysis showing transfection efficiency of siRNA c-jun in both PC-3 and LNCaP cells. (B) Cell proliferation in LNCaP (upper panel) and PC-3 (lower panel) cells transfected with c-jun siRNA or nontargeted (control) vector. Cells were treated with Doc for 24 and 48 hours. LNCaP cells harbor c-jun siRNA showed a significant decrease in proliferation (p=0.002) while PC-3 cells were not affected.
    Figure Legend Snippet: (A) Western blotting analysis showing transfection efficiency of siRNA c-jun in both PC-3 and LNCaP cells. (B) Cell proliferation in LNCaP (upper panel) and PC-3 (lower panel) cells transfected with c-jun siRNA or nontargeted (control) vector. Cells were treated with Doc for 24 and 48 hours. LNCaP cells harbor c-jun siRNA showed a significant decrease in proliferation (p=0.002) while PC-3 cells were not affected.

    Techniques Used: Western Blot, Transfection, Plasmid Preparation

    signalsilence c jun sirna ii  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc signalsilence c jun sirna ii
    Signalsilence C Jun Sirna Ii, supplied by Cell Signaling Technology Inc, 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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    jun sirna  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc jun sirna
    Jun Sirna, supplied by Cell Signaling Technology Inc, 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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    c jun  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc c jun
    C Jun, supplied by Cell Signaling Technology Inc, 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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    c jun 6205 sirnas  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc c jun 6205 sirnas
    C Jun 6205 Sirnas, supplied by Cell Signaling Technology Inc, 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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    C Jun Sirna, supplied by Cell Signaling Technology Inc, 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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    signalsilence c jun small interfering rnas sirnas  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc signalsilence c jun small interfering rnas sirnas
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    Densities of bands were quantified by Eagle Eye II software. GAPDH levels, measured in parallel, served as controls. Arsenite-transformed HELF cells were transfected with 50 nM of control <t>siRNA,</t> <t>NF-κB</t> <t>p65</t> siRNA, or c-Jun siRNA for 24 h. (A) Western blots and (B) relative protein levels (means ± SD, n = 3) of NF-κB p65 and c-Jun. (C) qRT-PCR analysis of miR-21 expression (means ± SD, n = 3). ** P <0.01 difference from Con siRNA group. (D) Western blots (upper) and RT-PCR (below) analyses for protein and mRNA levels and (E) relative protein levels (means ± SD, n = 3) of Pdcd4, Spry1, cleaved-caspase-3, and caspase-3, ** P <0.01 difference from the control (Con) siRNA group.
    C Jun Sirna, supplied by Cell Signaling Technology Inc, 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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    (A) Western blotting analysis showing transfection efficiency of siRNA c-jun in both PC-3 and LNCaP cells. (B) Cell proliferation in LNCaP (upper panel) and PC-3 (lower panel) cells transfected with c-jun siRNA or nontargeted (control) vector. Cells were treated with Doc for 24 and 48 hours. LNCaP cells harbor c-jun siRNA showed a significant decrease in proliferation (p=0.002) while PC-3 cells were not affected.
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    (A) Western blotting analysis showing transfection efficiency of siRNA c-jun in both PC-3 and LNCaP cells. (B) Cell proliferation in LNCaP (upper panel) and PC-3 (lower panel) cells transfected with c-jun siRNA or nontargeted (control) vector. Cells were treated with Doc for 24 and 48 hours. LNCaP cells harbor c-jun siRNA showed a significant decrease in proliferation (p=0.002) while PC-3 cells were not affected.
    Signalsilence C Jun Sirna Ii, supplied by Cell Signaling Technology Inc, 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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    (A) Western blotting analysis showing transfection efficiency of siRNA c-jun in both PC-3 and LNCaP cells. (B) Cell proliferation in LNCaP (upper panel) and PC-3 (lower panel) cells transfected with c-jun siRNA or nontargeted (control) vector. Cells were treated with Doc for 24 and 48 hours. LNCaP cells harbor c-jun siRNA showed a significant decrease in proliferation (p=0.002) while PC-3 cells were not affected.
    Jun Sirna, supplied by Cell Signaling Technology Inc, 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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    (A) Western blotting analysis showing transfection efficiency of siRNA c-jun in both PC-3 and LNCaP cells. (B) Cell proliferation in LNCaP (upper panel) and PC-3 (lower panel) cells transfected with c-jun siRNA or nontargeted (control) vector. Cells were treated with Doc for 24 and 48 hours. LNCaP cells harbor c-jun siRNA showed a significant decrease in proliferation (p=0.002) while PC-3 cells were not affected.
    C Jun 6205 Sirnas, supplied by Cell Signaling Technology Inc, 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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    Cell Signaling Technology Inc signalsilence c jun small interfering rnas sirnas
    (A) Western blotting analysis showing transfection efficiency of siRNA c-jun in both PC-3 and LNCaP cells. (B) Cell proliferation in LNCaP (upper panel) and PC-3 (lower panel) cells transfected with c-jun siRNA or nontargeted (control) vector. Cells were treated with Doc for 24 and 48 hours. LNCaP cells harbor c-jun siRNA showed a significant decrease in proliferation (p=0.002) while PC-3 cells were not affected.
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    Densities of bands were quantified by Eagle Eye II software. GAPDH levels, measured in parallel, served as controls. Arsenite-transformed HELF cells were transfected with 50 nM of control siRNA, NF-κB p65 siRNA, or c-Jun siRNA for 24 h. (A) Western blots and (B) relative protein levels (means ± SD, n = 3) of NF-κB p65 and c-Jun. (C) qRT-PCR analysis of miR-21 expression (means ± SD, n = 3). ** P <0.01 difference from Con siRNA group. (D) Western blots (upper) and RT-PCR (below) analyses for protein and mRNA levels and (E) relative protein levels (means ± SD, n = 3) of Pdcd4, Spry1, cleaved-caspase-3, and caspase-3, ** P <0.01 difference from the control (Con) siRNA group.

    Journal: PLoS ONE

    Article Title: Feedback Regulations of miR-21 and MAPKs via Pdcd4 and Spry1 Are Involved in Arsenite-Induced Cell Malignant Transformation

    doi: 10.1371/journal.pone.0057652

    Figure Lengend Snippet: Densities of bands were quantified by Eagle Eye II software. GAPDH levels, measured in parallel, served as controls. Arsenite-transformed HELF cells were transfected with 50 nM of control siRNA, NF-κB p65 siRNA, or c-Jun siRNA for 24 h. (A) Western blots and (B) relative protein levels (means ± SD, n = 3) of NF-κB p65 and c-Jun. (C) qRT-PCR analysis of miR-21 expression (means ± SD, n = 3). ** P <0.01 difference from Con siRNA group. (D) Western blots (upper) and RT-PCR (below) analyses for protein and mRNA levels and (E) relative protein levels (means ± SD, n = 3) of Pdcd4, Spry1, cleaved-caspase-3, and caspase-3, ** P <0.01 difference from the control (Con) siRNA group.

    Article Snippet: Control siRNA, NF-κB p65 siRNA, and c-Jun siRNA were purchased from Cell Signaling Technology.

    Techniques: Software, Transformation Assay, Transfection, Western Blot, Quantitative RT-PCR, Expressing, Reverse Transcription Polymerase Chain Reaction

    (A) Western blotting analysis showing transfection efficiency of siRNA c-jun in both PC-3 and LNCaP cells. (B) Cell proliferation in LNCaP (upper panel) and PC-3 (lower panel) cells transfected with c-jun siRNA or nontargeted (control) vector. Cells were treated with Doc for 24 and 48 hours. LNCaP cells harbor c-jun siRNA showed a significant decrease in proliferation (p=0.002) while PC-3 cells were not affected.

    Journal: PLoS ONE

    Article Title: Interaction between c-jun and Androgen Receptor Determines the Outcome of Taxane Therapy in Castration Resistant Prostate Cancer

    doi: 10.1371/journal.pone.0079573

    Figure Lengend Snippet: (A) Western blotting analysis showing transfection efficiency of siRNA c-jun in both PC-3 and LNCaP cells. (B) Cell proliferation in LNCaP (upper panel) and PC-3 (lower panel) cells transfected with c-jun siRNA or nontargeted (control) vector. Cells were treated with Doc for 24 and 48 hours. LNCaP cells harbor c-jun siRNA showed a significant decrease in proliferation (p=0.002) while PC-3 cells were not affected.

    Article Snippet: For siRNA experiments, PC-3 and LNCaP cells were transfected for 48 hours with 100 nM siRNA c-jun or non-targeting siRNA (Cell Signaling Technology, Danvers, MA, USA).

    Techniques: Western Blot, Transfection, Plasmid Preparation