phosphorylated extracellular signal regulated kinase perk 1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phosphorylated extracellular signal regulated kinase perk 1 2
    Phosphorylated Extracellular Signal Regulated Kinase Perk 1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    phosphorylated extracellular signal regulated kinase perk 1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phosphorylated extracellular signal regulated kinase perk 1 2
    Phosphorylated Extracellular Signal Regulated Kinase Perk 1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    extracellular signal regulated kinase erk 1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc extracellular signal regulated kinase erk 1 2
    Extracellular Signal Regulated Kinase Erk 1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    extracellular signal regulated kinase erk  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc extracellular signal regulated kinase erk
    LXA 4 <t>suppresses</t> <t>p38</t> and <t>ERK</t> signalling in airway epithelial cells (A, B) and NHNE cells (C, D). All experiments were performed using 5 donors, grown in duplicate, with 3-6 wells per condition. *p<0.05 compared to control.
    Extracellular Signal Regulated Kinase Erk, 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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    Images

    1) Product Images from "Exogenous Lipoxin A4 attenuates IL4-induced Mucin Expression in Human Airway Epithelial Cells"

    Article Title: Exogenous Lipoxin A4 attenuates IL4-induced Mucin Expression in Human Airway Epithelial Cells

    Journal: International Journal of Medical Sciences

    doi: 10.7150/ijms.79525

    LXA 4 suppresses p38 and ERK signalling in airway epithelial cells (A, B) and NHNE cells (C, D). All experiments were performed using 5 donors, grown in duplicate, with 3-6 wells per condition. *p<0.05 compared to control.
    Figure Legend Snippet: LXA 4 suppresses p38 and ERK signalling in airway epithelial cells (A, B) and NHNE cells (C, D). All experiments were performed using 5 donors, grown in duplicate, with 3-6 wells per condition. *p<0.05 compared to control.

    Techniques Used:

    regulation  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc regulation
    Regulation, 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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    regulation  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc regulation
    Regulation, 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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    regulation  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc regulation
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    ion regulation  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc ion regulation
    Ion Regulation, 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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    anti extracellular signal regulated kinase  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti extracellular signal regulated kinase
    Osteoprotegerin (OPG) regulates MAPK signaling pathway activity via DUSP14. ( A ) OPG and dual specificity phosphatase 14 (DUSP14) protein levels in the mice. ( B ) Phosphorylation levels of <t>extracellular</t> <t>signal-regulated</t> kinases (ERK), c-Jun N-terminal <t>kinase</t> 1 (JNK), and P38 in mouse liver. ( C ) OPG and DUSP14 proteins in OPG-overexpressing hepatocytes. ( D ) Phosphorylation levels of ERK, JNK, and P38 in OPG-overexpressing hepatocytes. ( E ) OPG and DUSP14 proteins in DUSP14 knockout hepatocytes. ( F ) Phosphorylation levels of ERK, JNK, and P38 in DUSP14 knockout hepatocytes. Each group at least has 3 samples. The data in ( A – F ) are presented as the mean ± SD; ns no significant difference, *p < 0.0, **p < 0.01, and ***p < 0.001.
    Anti Extracellular Signal Regulated Kinase, 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 "Osteoprotegerin deficiency aggravates methionine–choline-deficient diet-induced nonalcoholic steatohepatitis in mice"

    Article Title: Osteoprotegerin deficiency aggravates methionine–choline-deficient diet-induced nonalcoholic steatohepatitis in mice

    Journal: Scientific Reports

    doi: 10.1038/s41598-023-30001-7

    Osteoprotegerin (OPG) regulates MAPK signaling pathway activity via DUSP14. ( A ) OPG and dual specificity phosphatase 14 (DUSP14) protein levels in the mice. ( B ) Phosphorylation levels of extracellular signal-regulated kinases (ERK), c-Jun N-terminal kinase 1 (JNK), and P38 in mouse liver. ( C ) OPG and DUSP14 proteins in OPG-overexpressing hepatocytes. ( D ) Phosphorylation levels of ERK, JNK, and P38 in OPG-overexpressing hepatocytes. ( E ) OPG and DUSP14 proteins in DUSP14 knockout hepatocytes. ( F ) Phosphorylation levels of ERK, JNK, and P38 in DUSP14 knockout hepatocytes. Each group at least has 3 samples. The data in ( A – F ) are presented as the mean ± SD; ns no significant difference, *p < 0.0, **p < 0.01, and ***p < 0.001.
    Figure Legend Snippet: Osteoprotegerin (OPG) regulates MAPK signaling pathway activity via DUSP14. ( A ) OPG and dual specificity phosphatase 14 (DUSP14) protein levels in the mice. ( B ) Phosphorylation levels of extracellular signal-regulated kinases (ERK), c-Jun N-terminal kinase 1 (JNK), and P38 in mouse liver. ( C ) OPG and DUSP14 proteins in OPG-overexpressing hepatocytes. ( D ) Phosphorylation levels of ERK, JNK, and P38 in OPG-overexpressing hepatocytes. ( E ) OPG and DUSP14 proteins in DUSP14 knockout hepatocytes. ( F ) Phosphorylation levels of ERK, JNK, and P38 in DUSP14 knockout hepatocytes. Each group at least has 3 samples. The data in ( A – F ) are presented as the mean ± SD; ns no significant difference, *p < 0.0, **p < 0.01, and ***p < 0.001.

    Techniques Used: Activity Assay, Knock-Out

    phospho extracellular signal regulated kinase p erk  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho extracellular signal regulated kinase p erk
    Effect of Helixor-M on the MAPK signaling pathway in LPS-induced RAW 264.7 cells. The cells were pretreated with Helixor-M (5–500 μg/mL) and incubated with LPS (1 μg/mL) for 24 h. The protein levels of ( A ) p-JNK/JNK, ( B ) <t>p-ERK/ERK,</t> and ( C ) p-p38/p38 were examined using Western blot analysis. Quantification of each protein was determined using ImageJ software. Data are expressed as means ± SEM (n = 6). Compared with the control group: ** p < 0.01, **** p < 0.0001; compared with the LPS group: N.S (not significance), ## p < 0.01.
    Phospho Extracellular Signal Regulated Kinase P Erk, 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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    Images

    1) Product Images from "Helixor-M Suppresses Immunostimulatory Activity through TLR4-Dependent NF-κB Pathway in RAW 264.7 Cells"

    Article Title: Helixor-M Suppresses Immunostimulatory Activity through TLR4-Dependent NF-κB Pathway in RAW 264.7 Cells

    Journal: Life

    doi: 10.3390/life13020595

    Effect of Helixor-M on the MAPK signaling pathway in LPS-induced RAW 264.7 cells. The cells were pretreated with Helixor-M (5–500 μg/mL) and incubated with LPS (1 μg/mL) for 24 h. The protein levels of ( A ) p-JNK/JNK, ( B ) p-ERK/ERK, and ( C ) p-p38/p38 were examined using Western blot analysis. Quantification of each protein was determined using ImageJ software. Data are expressed as means ± SEM (n = 6). Compared with the control group: ** p < 0.01, **** p < 0.0001; compared with the LPS group: N.S (not significance), ## p < 0.01.
    Figure Legend Snippet: Effect of Helixor-M on the MAPK signaling pathway in LPS-induced RAW 264.7 cells. The cells were pretreated with Helixor-M (5–500 μg/mL) and incubated with LPS (1 μg/mL) for 24 h. The protein levels of ( A ) p-JNK/JNK, ( B ) p-ERK/ERK, and ( C ) p-p38/p38 were examined using Western blot analysis. Quantification of each protein was determined using ImageJ software. Data are expressed as means ± SEM (n = 6). Compared with the control group: ** p < 0.01, **** p < 0.0001; compared with the LPS group: N.S (not significance), ## p < 0.01.

    Techniques Used: Incubation, Western Blot, Software

    ionic regulation  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc ionic regulation
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    Cell Signaling Technology Inc phosphorylated extracellular signal regulated kinase perk 1 2
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    LXA 4 <t>suppresses</t> <t>p38</t> and <t>ERK</t> signalling in airway epithelial cells (A, B) and NHNE cells (C, D). All experiments were performed using 5 donors, grown in duplicate, with 3-6 wells per condition. *p<0.05 compared to control.
    Extracellular Signal Regulated Kinase Erk, 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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    LXA 4 <t>suppresses</t> <t>p38</t> and <t>ERK</t> signalling in airway epithelial cells (A, B) and NHNE cells (C, D). All experiments were performed using 5 donors, grown in duplicate, with 3-6 wells per condition. *p<0.05 compared to control.
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    LXA 4 <t>suppresses</t> <t>p38</t> and <t>ERK</t> signalling in airway epithelial cells (A, B) and NHNE cells (C, D). All experiments were performed using 5 donors, grown in duplicate, with 3-6 wells per condition. *p<0.05 compared to control.
    Ion Regulation, 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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    Cell Signaling Technology Inc anti extracellular signal regulated kinase
    Osteoprotegerin (OPG) regulates MAPK signaling pathway activity via DUSP14. ( A ) OPG and dual specificity phosphatase 14 (DUSP14) protein levels in the mice. ( B ) Phosphorylation levels of <t>extracellular</t> <t>signal-regulated</t> kinases (ERK), c-Jun N-terminal <t>kinase</t> 1 (JNK), and P38 in mouse liver. ( C ) OPG and DUSP14 proteins in OPG-overexpressing hepatocytes. ( D ) Phosphorylation levels of ERK, JNK, and P38 in OPG-overexpressing hepatocytes. ( E ) OPG and DUSP14 proteins in DUSP14 knockout hepatocytes. ( F ) Phosphorylation levels of ERK, JNK, and P38 in DUSP14 knockout hepatocytes. Each group at least has 3 samples. The data in ( A – F ) are presented as the mean ± SD; ns no significant difference, *p < 0.0, **p < 0.01, and ***p < 0.001.
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    Cell Signaling Technology Inc phospho extracellular signal regulated kinase p erk
    Effect of Helixor-M on the MAPK signaling pathway in LPS-induced RAW 264.7 cells. The cells were pretreated with Helixor-M (5–500 μg/mL) and incubated with LPS (1 μg/mL) for 24 h. The protein levels of ( A ) p-JNK/JNK, ( B ) <t>p-ERK/ERK,</t> and ( C ) p-p38/p38 were examined using Western blot analysis. Quantification of each protein was determined using ImageJ software. Data are expressed as means ± SEM (n = 6). Compared with the control group: ** p < 0.01, **** p < 0.0001; compared with the LPS group: N.S (not significance), ## p < 0.01.
    Phospho Extracellular Signal Regulated Kinase P Erk, 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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    Effect of Helixor-M on the MAPK signaling pathway in LPS-induced RAW 264.7 cells. The cells were pretreated with Helixor-M (5–500 μg/mL) and incubated with LPS (1 μg/mL) for 24 h. The protein levels of ( A ) p-JNK/JNK, ( B ) <t>p-ERK/ERK,</t> and ( C ) p-p38/p38 were examined using Western blot analysis. Quantification of each protein was determined using ImageJ software. Data are expressed as means ± SEM (n = 6). Compared with the control group: ** p < 0.01, **** p < 0.0001; compared with the LPS group: N.S (not significance), ## p < 0.01.
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    Image Search Results


    LXA 4 suppresses p38 and ERK signalling in airway epithelial cells (A, B) and NHNE cells (C, D). All experiments were performed using 5 donors, grown in duplicate, with 3-6 wells per condition. *p<0.05 compared to control.

    Journal: International Journal of Medical Sciences

    Article Title: Exogenous Lipoxin A4 attenuates IL4-induced Mucin Expression in Human Airway Epithelial Cells

    doi: 10.7150/ijms.79525

    Figure Lengend Snippet: LXA 4 suppresses p38 and ERK signalling in airway epithelial cells (A, B) and NHNE cells (C, D). All experiments were performed using 5 donors, grown in duplicate, with 3-6 wells per condition. *p<0.05 compared to control.

    Article Snippet: Antibodies against p38, extracellular signal-regulated kinase (ERK), JNK, and phospho-p38 were from Cell Signaling Technology (Danvers, MA, USA).

    Techniques:

    Osteoprotegerin (OPG) regulates MAPK signaling pathway activity via DUSP14. ( A ) OPG and dual specificity phosphatase 14 (DUSP14) protein levels in the mice. ( B ) Phosphorylation levels of extracellular signal-regulated kinases (ERK), c-Jun N-terminal kinase 1 (JNK), and P38 in mouse liver. ( C ) OPG and DUSP14 proteins in OPG-overexpressing hepatocytes. ( D ) Phosphorylation levels of ERK, JNK, and P38 in OPG-overexpressing hepatocytes. ( E ) OPG and DUSP14 proteins in DUSP14 knockout hepatocytes. ( F ) Phosphorylation levels of ERK, JNK, and P38 in DUSP14 knockout hepatocytes. Each group at least has 3 samples. The data in ( A – F ) are presented as the mean ± SD; ns no significant difference, *p < 0.0, **p < 0.01, and ***p < 0.001.

    Journal: Scientific Reports

    Article Title: Osteoprotegerin deficiency aggravates methionine–choline-deficient diet-induced nonalcoholic steatohepatitis in mice

    doi: 10.1038/s41598-023-30001-7

    Figure Lengend Snippet: Osteoprotegerin (OPG) regulates MAPK signaling pathway activity via DUSP14. ( A ) OPG and dual specificity phosphatase 14 (DUSP14) protein levels in the mice. ( B ) Phosphorylation levels of extracellular signal-regulated kinases (ERK), c-Jun N-terminal kinase 1 (JNK), and P38 in mouse liver. ( C ) OPG and DUSP14 proteins in OPG-overexpressing hepatocytes. ( D ) Phosphorylation levels of ERK, JNK, and P38 in OPG-overexpressing hepatocytes. ( E ) OPG and DUSP14 proteins in DUSP14 knockout hepatocytes. ( F ) Phosphorylation levels of ERK, JNK, and P38 in DUSP14 knockout hepatocytes. Each group at least has 3 samples. The data in ( A – F ) are presented as the mean ± SD; ns no significant difference, *p < 0.0, **p < 0.01, and ***p < 0.001.

    Article Snippet: Primary antibodies included anti-OPG (#sc-390518, Santa Cruz Biotechnology), anti-DUSP14 (#ab272587, Abcam), anti-extracellular signal-regulated kinase (ERK, # 4695, Cell Signaling Technology), anti-phospho-ERK (#4370, Cell Signaling Technology), anti-P38 (#9212, Cell Signaling Technology), anti-phospho-P38 (#4511, Cell Signaling Technology), anti-c-Jun NH2-terminal kinase (JNK, #9252, Cell Signaling Technology), anti-phospho-JNK (#4668, Cell Signaling Technology), and anti-β-actin (#TA-09, ZSGB-BIO, China) antibodies.

    Techniques: Activity Assay, Knock-Out

    Effect of Helixor-M on the MAPK signaling pathway in LPS-induced RAW 264.7 cells. The cells were pretreated with Helixor-M (5–500 μg/mL) and incubated with LPS (1 μg/mL) for 24 h. The protein levels of ( A ) p-JNK/JNK, ( B ) p-ERK/ERK, and ( C ) p-p38/p38 were examined using Western blot analysis. Quantification of each protein was determined using ImageJ software. Data are expressed as means ± SEM (n = 6). Compared with the control group: ** p < 0.01, **** p < 0.0001; compared with the LPS group: N.S (not significance), ## p < 0.01.

    Journal: Life

    Article Title: Helixor-M Suppresses Immunostimulatory Activity through TLR4-Dependent NF-κB Pathway in RAW 264.7 Cells

    doi: 10.3390/life13020595

    Figure Lengend Snippet: Effect of Helixor-M on the MAPK signaling pathway in LPS-induced RAW 264.7 cells. The cells were pretreated with Helixor-M (5–500 μg/mL) and incubated with LPS (1 μg/mL) for 24 h. The protein levels of ( A ) p-JNK/JNK, ( B ) p-ERK/ERK, and ( C ) p-p38/p38 were examined using Western blot analysis. Quantification of each protein was determined using ImageJ software. Data are expressed as means ± SEM (n = 6). Compared with the control group: ** p < 0.01, **** p < 0.0001; compared with the LPS group: N.S (not significance), ## p < 0.01.

    Article Snippet: Primary antibodies against rabbit-anti COX-2, NF-κB p65, ERK, phospho-extracellular signal-regulated kinase (p-ERK), p38, p-p38, JNK, phospho-Jun N-terminal (p-JNK), phosphoinositide 3-kinase (PI3K), p-AKT, AKT, and Lamin B1 were purchased from Cell Signaling Technology (Beverly, MA, USA).

    Techniques: Incubation, Western Blot, Software