rabbit polyclonal antibodies against erk 1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit polyclonal antibodies against erk 1 2
    Rabbit Polyclonal Antibodies Against Erk 1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    antibodies against ap2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc antibodies against ap2
    ( A ) Schematic representation of C3H10T1/2 MSCs differentiation timeline. ( B ) mRNA expression levels of the major thermogenic markers Ucp1 , Pgc1α , Prdm16 and Pparγ after DS0908 and DS0950 treatment in differentiated C3H10T1/2 mesenchymal stem cells (MSCs). ( C ) Thermogenic marker UCP1, PPARγ, PGC1α and PRDM16 protein expression levels after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. ( D and E ) mRNA expression levels of beige ( Cd137 , Fgf21 , P2rx5 and Tbx1 ), brown ( Cox2 ) and white ( <t>aP2</t> , Psat1 , Resistin and Serpina3k ) adipocyte-specific markers after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. Tbp was used as an internal control gene and β‐actin as a protein loading control. The data from three individual experiments are expressed as the average ± standard error mean (SEM). *, **, *** and ns indicate p < 0.05, < 0.01, < 0.001 and non-significant, respectively, to express the statistically significant differences between the control (MDI) and the treatment groups in the figures. The protein band intensities were measured using ImageJ. Adipogenic differentiation medium, MDI: 0.5mM IBMX, 1 μM dexamethasone and 10 μg/ml insulin; 1 μM Rosiglitazone (Rosi); DS0908 = B. bifidum DS0908; DS0950 = B. longum DS0950.
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    1) Product Images from "Bifidobacterium bifidum DS0908 and Bifidobacterium longum DS0950 Culture-Supernatants Ameliorate Obesity-Related Characteristics in Mice with High-Fat Diet-Induced Obesity"

    Article Title: Bifidobacterium bifidum DS0908 and Bifidobacterium longum DS0950 Culture-Supernatants Ameliorate Obesity-Related Characteristics in Mice with High-Fat Diet-Induced Obesity

    Journal: Journal of Microbiology and Biotechnology

    doi: 10.4014/jmb.2210.10046

    ( A ) Schematic representation of C3H10T1/2 MSCs differentiation timeline. ( B ) mRNA expression levels of the major thermogenic markers Ucp1 , Pgc1α , Prdm16 and Pparγ after DS0908 and DS0950 treatment in differentiated C3H10T1/2 mesenchymal stem cells (MSCs). ( C ) Thermogenic marker UCP1, PPARγ, PGC1α and PRDM16 protein expression levels after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. ( D and E ) mRNA expression levels of beige ( Cd137 , Fgf21 , P2rx5 and Tbx1 ), brown ( Cox2 ) and white ( aP2 , Psat1 , Resistin and Serpina3k ) adipocyte-specific markers after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. Tbp was used as an internal control gene and β‐actin as a protein loading control. The data from three individual experiments are expressed as the average ± standard error mean (SEM). *, **, *** and ns indicate p < 0.05, < 0.01, < 0.001 and non-significant, respectively, to express the statistically significant differences between the control (MDI) and the treatment groups in the figures. The protein band intensities were measured using ImageJ. Adipogenic differentiation medium, MDI: 0.5mM IBMX, 1 μM dexamethasone and 10 μg/ml insulin; 1 μM Rosiglitazone (Rosi); DS0908 = B. bifidum DS0908; DS0950 = B. longum DS0950.
    Figure Legend Snippet: ( A ) Schematic representation of C3H10T1/2 MSCs differentiation timeline. ( B ) mRNA expression levels of the major thermogenic markers Ucp1 , Pgc1α , Prdm16 and Pparγ after DS0908 and DS0950 treatment in differentiated C3H10T1/2 mesenchymal stem cells (MSCs). ( C ) Thermogenic marker UCP1, PPARγ, PGC1α and PRDM16 protein expression levels after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. ( D and E ) mRNA expression levels of beige ( Cd137 , Fgf21 , P2rx5 and Tbx1 ), brown ( Cox2 ) and white ( aP2 , Psat1 , Resistin and Serpina3k ) adipocyte-specific markers after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. Tbp was used as an internal control gene and β‐actin as a protein loading control. The data from three individual experiments are expressed as the average ± standard error mean (SEM). *, **, *** and ns indicate p < 0.05, < 0.01, < 0.001 and non-significant, respectively, to express the statistically significant differences between the control (MDI) and the treatment groups in the figures. The protein band intensities were measured using ImageJ. Adipogenic differentiation medium, MDI: 0.5mM IBMX, 1 μM dexamethasone and 10 μg/ml insulin; 1 μM Rosiglitazone (Rosi); DS0908 = B. bifidum DS0908; DS0950 = B. longum DS0950.

    Techniques Used: Expressing, Marker

    rabbit polyclonal antibodies against erk 1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit polyclonal antibodies against erk 1 2
    Rabbit Polyclonal Antibodies Against Erk 1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rabbit polyclonal antibodies against erk 1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit polyclonal antibodies against erk 1 2
    Cells overexpressing LPA 1 (black, circles), LPA 2 (blue, squares) or LPA 3 (red, triangles) receptors were incubated for the times indicated in the presence of 1 μM LPA, incubation was terminated and <t>phospho-ERK</t> <t>1/2</t> (pERK) and total ERK 1/2 (ERK) were assayed by Western blotting. Plotted are the increases in phospho-ERK 1/2 as mean ± S. E. M. of 4–5 experiments using different cell preparations. Representative Western blots are presented for the different receptor subtypes.
    Rabbit Polyclonal Antibodies Against Erk 1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Phosphorylation and Internalization of Lysophosphatidic Acid Receptors LPA 1 , LPA 2 , and LPA 3"

    Article Title: Phosphorylation and Internalization of Lysophosphatidic Acid Receptors LPA 1 , LPA 2 , and LPA 3

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0140583

    Cells overexpressing LPA 1 (black, circles), LPA 2 (blue, squares) or LPA 3 (red, triangles) receptors were incubated for the times indicated in the presence of 1 μM LPA, incubation was terminated and phospho-ERK 1/2 (pERK) and total ERK 1/2 (ERK) were assayed by Western blotting. Plotted are the increases in phospho-ERK 1/2 as mean ± S. E. M. of 4–5 experiments using different cell preparations. Representative Western blots are presented for the different receptor subtypes.
    Figure Legend Snippet: Cells overexpressing LPA 1 (black, circles), LPA 2 (blue, squares) or LPA 3 (red, triangles) receptors were incubated for the times indicated in the presence of 1 μM LPA, incubation was terminated and phospho-ERK 1/2 (pERK) and total ERK 1/2 (ERK) were assayed by Western blotting. Plotted are the increases in phospho-ERK 1/2 as mean ± S. E. M. of 4–5 experiments using different cell preparations. Representative Western blots are presented for the different receptor subtypes.

    Techniques Used: Incubation, Western Blot

    Cells overexpressing LPA 1 (panels A and D), LPA 2 (panels B and E) or LPA 3 (panels C and F) receptors were incubated in the absence or presence of 10 μM AG1478 (AG) for 30 min and then challenged with 1 μM LPA (panels A-C) or 100 ng/ml EGF (panels D-F) for 5 min; incubation was terminated and phospho-ERK 1/2 (pERK) and total ERK 1/2 (ERK) were assayed by Western blotting. Plotted are the increases in phospho-ERK 1/2 as mean ± S. E. M. of 4–5 experiments using different cell preparations. Representative Western blots are presented for the different receptor subtypes. *p < 0.001 vs. baseline (B); ** p <0.001 vs. LPA or EGF alone.
    Figure Legend Snippet: Cells overexpressing LPA 1 (panels A and D), LPA 2 (panels B and E) or LPA 3 (panels C and F) receptors were incubated in the absence or presence of 10 μM AG1478 (AG) for 30 min and then challenged with 1 μM LPA (panels A-C) or 100 ng/ml EGF (panels D-F) for 5 min; incubation was terminated and phospho-ERK 1/2 (pERK) and total ERK 1/2 (ERK) were assayed by Western blotting. Plotted are the increases in phospho-ERK 1/2 as mean ± S. E. M. of 4–5 experiments using different cell preparations. Representative Western blots are presented for the different receptor subtypes. *p < 0.001 vs. baseline (B); ** p <0.001 vs. LPA or EGF alone.

    Techniques Used: Incubation, Western Blot

    rabbit antibodies against perk1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit antibodies against perk1 2
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    rabbit antibodies against perk1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit antibodies against perk1 2
    Rabbit Antibodies Against Perk1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rabbit antibody against erk1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit antibody against erk1 2
    Rabbit Antibody Against Erk1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rabbit antibodies against pjnk  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit antibodies against pjnk
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    rabbit polyclonal antibodies against diphosphoerk1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit polyclonal antibodies against diphosphoerk1 2
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    rabbit antibodies against perk1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit antibodies against perk1 2
    Rabbit Antibodies Against Perk1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rabbit antibodies against perk1 2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit antibodies against perk1 2
    ERK1/2 phosphorylation by coactivation of NMDARs and group I mGluRs with the specific agonists at their low dose range in cultured rat striatal neurons. A, Coadministration of NMDA and DHPG at 1 and 3 μm (5 min) induced a robust increase in <t>pERK1/2</t> but not ERK1/2 levels, whereas the two agonist applications alone at the same concentrations for 5 min did not change pERK1/2 and ERK1/2 levels. Representative immunoblots are shown left of the quantified data of pERK2 analyzed from separate experiments (mean ± SEM; n = 8-10). +p < 0.05 versus NMDA and DHPG alone at the corresponding concentration. B, NMDA/DHPG caused a rapid and transient increase in pERK1/2 levels without changing ERK1/2 levels. The two drugs at 1-3 μm were added to cultures and incubated for different durations. Representative immunoblots are shown left of the quantified data (mean ± SEM; n = 5). *p < 0.05 versus basal levels. C, Confocal immunofluorescent images illustrating subcellular distributions of pERK1/2 induced by NMDA/DHPG (3 μm; 5 min). Strong pERK1/2 immunostaining is present in the nucleus, and weak to moderate staining is present in the cytoplasm and neural processes.
    Rabbit Antibodies Against Perk1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "A Novel Ca 2+ -Independent Signaling Pathway to Extracellular Signal-Regulated Protein Kinase by Coactivation of NMDA Receptors and Metabotropic Glutamate Receptor 5 in Neurons"

    Article Title: A Novel Ca 2+ -Independent Signaling Pathway to Extracellular Signal-Regulated Protein Kinase by Coactivation of NMDA Receptors and Metabotropic Glutamate Receptor 5 in Neurons

    Journal: The Journal of Neuroscience

    doi: 10.1523/JNEUROSCI.2496-04.2004

    ERK1/2 phosphorylation by coactivation of NMDARs and group I mGluRs with the specific agonists at their low dose range in cultured rat striatal neurons. A, Coadministration of NMDA and DHPG at 1 and 3 μm (5 min) induced a robust increase in pERK1/2 but not ERK1/2 levels, whereas the two agonist applications alone at the same concentrations for 5 min did not change pERK1/2 and ERK1/2 levels. Representative immunoblots are shown left of the quantified data of pERK2 analyzed from separate experiments (mean ± SEM; n = 8-10). +p < 0.05 versus NMDA and DHPG alone at the corresponding concentration. B, NMDA/DHPG caused a rapid and transient increase in pERK1/2 levels without changing ERK1/2 levels. The two drugs at 1-3 μm were added to cultures and incubated for different durations. Representative immunoblots are shown left of the quantified data (mean ± SEM; n = 5). *p < 0.05 versus basal levels. C, Confocal immunofluorescent images illustrating subcellular distributions of pERK1/2 induced by NMDA/DHPG (3 μm; 5 min). Strong pERK1/2 immunostaining is present in the nucleus, and weak to moderate staining is present in the cytoplasm and neural processes.
    Figure Legend Snippet: ERK1/2 phosphorylation by coactivation of NMDARs and group I mGluRs with the specific agonists at their low dose range in cultured rat striatal neurons. A, Coadministration of NMDA and DHPG at 1 and 3 μm (5 min) induced a robust increase in pERK1/2 but not ERK1/2 levels, whereas the two agonist applications alone at the same concentrations for 5 min did not change pERK1/2 and ERK1/2 levels. Representative immunoblots are shown left of the quantified data of pERK2 analyzed from separate experiments (mean ± SEM; n = 8-10). +p < 0.05 versus NMDA and DHPG alone at the corresponding concentration. B, NMDA/DHPG caused a rapid and transient increase in pERK1/2 levels without changing ERK1/2 levels. The two drugs at 1-3 μm were added to cultures and incubated for different durations. Representative immunoblots are shown left of the quantified data (mean ± SEM; n = 5). *p < 0.05 versus basal levels. C, Confocal immunofluorescent images illustrating subcellular distributions of pERK1/2 induced by NMDA/DHPG (3 μm; 5 min). Strong pERK1/2 immunostaining is present in the nucleus, and weak to moderate staining is present in the cytoplasm and neural processes.

    Techniques Used: Cell Culture, Western Blot, Concentration Assay, Incubation, Immunostaining, Staining

    Effects of the MEK inhibitor U0126 on the NMDA/DHPG (N/D)-induced phosphorylation of ERK1/2, Elk-1, and CREB and c-Fos expression in cultured rat striatal neurons. Note that U0126 blocked the NMDA/DHPG-induced phosphorylation of ERK1/2 (A), Elk-1 (B), and CREB (C) and c-Fos expression (D), without changing cellular levels of the three proteins. U0126 (1 μm) was incubated 30 min before and during treatment with NMDA (3 μm) and DHPG (3 μm) for 5 min (pERK1/2), 15 min (pElk-1 and pCREB), or 30 min (c-Fos). Representative immunoblots are shown left to the quantified data (mean ± SEM; n = 4-5). *p < 0.05 versus basal levels; +p < 0.05 versus NMDA plus DHPG.
    Figure Legend Snippet: Effects of the MEK inhibitor U0126 on the NMDA/DHPG (N/D)-induced phosphorylation of ERK1/2, Elk-1, and CREB and c-Fos expression in cultured rat striatal neurons. Note that U0126 blocked the NMDA/DHPG-induced phosphorylation of ERK1/2 (A), Elk-1 (B), and CREB (C) and c-Fos expression (D), without changing cellular levels of the three proteins. U0126 (1 μm) was incubated 30 min before and during treatment with NMDA (3 μm) and DHPG (3 μm) for 5 min (pERK1/2), 15 min (pElk-1 and pCREB), or 30 min (c-Fos). Representative immunoblots are shown left to the quantified data (mean ± SEM; n = 4-5). *p < 0.05 versus basal levels; +p < 0.05 versus NMDA plus DHPG.

    Techniques Used: Expressing, Cell Culture, Incubation, Western Blot

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    Cell Signaling Technology Inc rabbit polyclonal antibodies against erk 1 2
    Rabbit Polyclonal Antibodies Against Erk 1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc antibodies against ap2
    ( A ) Schematic representation of C3H10T1/2 MSCs differentiation timeline. ( B ) mRNA expression levels of the major thermogenic markers Ucp1 , Pgc1α , Prdm16 and Pparγ after DS0908 and DS0950 treatment in differentiated C3H10T1/2 mesenchymal stem cells (MSCs). ( C ) Thermogenic marker UCP1, PPARγ, PGC1α and PRDM16 protein expression levels after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. ( D and E ) mRNA expression levels of beige ( Cd137 , Fgf21 , P2rx5 and Tbx1 ), brown ( Cox2 ) and white ( <t>aP2</t> , Psat1 , Resistin and Serpina3k ) adipocyte-specific markers after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. Tbp was used as an internal control gene and β‐actin as a protein loading control. The data from three individual experiments are expressed as the average ± standard error mean (SEM). *, **, *** and ns indicate p < 0.05, < 0.01, < 0.001 and non-significant, respectively, to express the statistically significant differences between the control (MDI) and the treatment groups in the figures. The protein band intensities were measured using ImageJ. Adipogenic differentiation medium, MDI: 0.5mM IBMX, 1 μM dexamethasone and 10 μg/ml insulin; 1 μM Rosiglitazone (Rosi); DS0908 = B. bifidum DS0908; DS0950 = B. longum DS0950.
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    ( A ) Schematic representation of C3H10T1/2 MSCs differentiation timeline. ( B ) mRNA expression levels of the major thermogenic markers Ucp1 , Pgc1α , Prdm16 and Pparγ after DS0908 and DS0950 treatment in differentiated C3H10T1/2 mesenchymal stem cells (MSCs). ( C ) Thermogenic marker UCP1, PPARγ, PGC1α and PRDM16 protein expression levels after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. ( D and E ) mRNA expression levels of beige ( Cd137 , Fgf21 , P2rx5 and Tbx1 ), brown ( Cox2 ) and white ( <t>aP2</t> , Psat1 , Resistin and Serpina3k ) adipocyte-specific markers after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. Tbp was used as an internal control gene and β‐actin as a protein loading control. The data from three individual experiments are expressed as the average ± standard error mean (SEM). *, **, *** and ns indicate p < 0.05, < 0.01, < 0.001 and non-significant, respectively, to express the statistically significant differences between the control (MDI) and the treatment groups in the figures. The protein band intensities were measured using ImageJ. Adipogenic differentiation medium, MDI: 0.5mM IBMX, 1 μM dexamethasone and 10 μg/ml insulin; 1 μM Rosiglitazone (Rosi); DS0908 = B. bifidum DS0908; DS0950 = B. longum DS0950.
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    ( A ) Schematic representation of C3H10T1/2 MSCs differentiation timeline. ( B ) mRNA expression levels of the major thermogenic markers Ucp1 , Pgc1α , Prdm16 and Pparγ after DS0908 and DS0950 treatment in differentiated C3H10T1/2 mesenchymal stem cells (MSCs). ( C ) Thermogenic marker UCP1, PPARγ, PGC1α and PRDM16 protein expression levels after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. ( D and E ) mRNA expression levels of beige ( Cd137 , Fgf21 , P2rx5 and Tbx1 ), brown ( Cox2 ) and white ( <t>aP2</t> , Psat1 , Resistin and Serpina3k ) adipocyte-specific markers after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. Tbp was used as an internal control gene and β‐actin as a protein loading control. The data from three individual experiments are expressed as the average ± standard error mean (SEM). *, **, *** and ns indicate p < 0.05, < 0.01, < 0.001 and non-significant, respectively, to express the statistically significant differences between the control (MDI) and the treatment groups in the figures. The protein band intensities were measured using ImageJ. Adipogenic differentiation medium, MDI: 0.5mM IBMX, 1 μM dexamethasone and 10 μg/ml insulin; 1 μM Rosiglitazone (Rosi); DS0908 = B. bifidum DS0908; DS0950 = B. longum DS0950.
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    ( A ) Schematic representation of C3H10T1/2 MSCs differentiation timeline. ( B ) mRNA expression levels of the major thermogenic markers Ucp1 , Pgc1α , Prdm16 and Pparγ after DS0908 and DS0950 treatment in differentiated C3H10T1/2 mesenchymal stem cells (MSCs). ( C ) Thermogenic marker UCP1, PPARγ, PGC1α and PRDM16 protein expression levels after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. ( D and E ) mRNA expression levels of beige ( Cd137 , Fgf21 , P2rx5 and Tbx1 ), brown ( Cox2 ) and white ( <t>aP2</t> , Psat1 , Resistin and Serpina3k ) adipocyte-specific markers after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. Tbp was used as an internal control gene and β‐actin as a protein loading control. The data from three individual experiments are expressed as the average ± standard error mean (SEM). *, **, *** and ns indicate p < 0.05, < 0.01, < 0.001 and non-significant, respectively, to express the statistically significant differences between the control (MDI) and the treatment groups in the figures. The protein band intensities were measured using ImageJ. Adipogenic differentiation medium, MDI: 0.5mM IBMX, 1 μM dexamethasone and 10 μg/ml insulin; 1 μM Rosiglitazone (Rosi); DS0908 = B. bifidum DS0908; DS0950 = B. longum DS0950.
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    Cell Signaling Technology Inc rabbit polyclonal antibodies against diphosphoerk1 2
    ( A ) Schematic representation of C3H10T1/2 MSCs differentiation timeline. ( B ) mRNA expression levels of the major thermogenic markers Ucp1 , Pgc1α , Prdm16 and Pparγ after DS0908 and DS0950 treatment in differentiated C3H10T1/2 mesenchymal stem cells (MSCs). ( C ) Thermogenic marker UCP1, PPARγ, PGC1α and PRDM16 protein expression levels after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. ( D and E ) mRNA expression levels of beige ( Cd137 , Fgf21 , P2rx5 and Tbx1 ), brown ( Cox2 ) and white ( <t>aP2</t> , Psat1 , Resistin and Serpina3k ) adipocyte-specific markers after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. Tbp was used as an internal control gene and β‐actin as a protein loading control. The data from three individual experiments are expressed as the average ± standard error mean (SEM). *, **, *** and ns indicate p < 0.05, < 0.01, < 0.001 and non-significant, respectively, to express the statistically significant differences between the control (MDI) and the treatment groups in the figures. The protein band intensities were measured using ImageJ. Adipogenic differentiation medium, MDI: 0.5mM IBMX, 1 μM dexamethasone and 10 μg/ml insulin; 1 μM Rosiglitazone (Rosi); DS0908 = B. bifidum DS0908; DS0950 = B. longum DS0950.
    Rabbit Polyclonal Antibodies Against Diphosphoerk1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    ( A ) Schematic representation of C3H10T1/2 MSCs differentiation timeline. ( B ) mRNA expression levels of the major thermogenic markers Ucp1 , Pgc1α , Prdm16 and Pparγ after DS0908 and DS0950 treatment in differentiated C3H10T1/2 mesenchymal stem cells (MSCs). ( C ) Thermogenic marker UCP1, PPARγ, PGC1α and PRDM16 protein expression levels after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. ( D and E ) mRNA expression levels of beige ( Cd137 , Fgf21 , P2rx5 and Tbx1 ), brown ( Cox2 ) and white ( aP2 , Psat1 , Resistin and Serpina3k ) adipocyte-specific markers after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. Tbp was used as an internal control gene and β‐actin as a protein loading control. The data from three individual experiments are expressed as the average ± standard error mean (SEM). *, **, *** and ns indicate p < 0.05, < 0.01, < 0.001 and non-significant, respectively, to express the statistically significant differences between the control (MDI) and the treatment groups in the figures. The protein band intensities were measured using ImageJ. Adipogenic differentiation medium, MDI: 0.5mM IBMX, 1 μM dexamethasone and 10 μg/ml insulin; 1 μM Rosiglitazone (Rosi); DS0908 = B. bifidum DS0908; DS0950 = B. longum DS0950.

    Journal: Journal of Microbiology and Biotechnology

    Article Title: Bifidobacterium bifidum DS0908 and Bifidobacterium longum DS0950 Culture-Supernatants Ameliorate Obesity-Related Characteristics in Mice with High-Fat Diet-Induced Obesity

    doi: 10.4014/jmb.2210.10046

    Figure Lengend Snippet: ( A ) Schematic representation of C3H10T1/2 MSCs differentiation timeline. ( B ) mRNA expression levels of the major thermogenic markers Ucp1 , Pgc1α , Prdm16 and Pparγ after DS0908 and DS0950 treatment in differentiated C3H10T1/2 mesenchymal stem cells (MSCs). ( C ) Thermogenic marker UCP1, PPARγ, PGC1α and PRDM16 protein expression levels after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. ( D and E ) mRNA expression levels of beige ( Cd137 , Fgf21 , P2rx5 and Tbx1 ), brown ( Cox2 ) and white ( aP2 , Psat1 , Resistin and Serpina3k ) adipocyte-specific markers after DS0908 and DS0950 treatments in differentiated C3H10T1/2 MSCs. Tbp was used as an internal control gene and β‐actin as a protein loading control. The data from three individual experiments are expressed as the average ± standard error mean (SEM). *, **, *** and ns indicate p < 0.05, < 0.01, < 0.001 and non-significant, respectively, to express the statistically significant differences between the control (MDI) and the treatment groups in the figures. The protein band intensities were measured using ImageJ. Adipogenic differentiation medium, MDI: 0.5mM IBMX, 1 μM dexamethasone and 10 μg/ml insulin; 1 μM Rosiglitazone (Rosi); DS0908 = B. bifidum DS0908; DS0950 = B. longum DS0950.

    Article Snippet: Antibodies against aP2 , AMPK, p-AMPK (Thr172), p38 MAPK, p-p38 MAPK (Thr180/Tyr182), p-CREB (Ser133), p-PKA substrate and anti-rabbit IgG anti-mouse IgG antibodies conjugated with horseradish peroxidase were acquired from Cell Signaling Technology (USA).

    Techniques: Expressing, Marker