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anti peroxisome proliferator activated receptor alpha  (Novus Biologicals)


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    Structured Review

    Novus Biologicals anti peroxisome proliferator activated receptor alpha
    Anti Peroxisome Proliferator Activated Receptor Alpha, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nb600+636/pm41887219-989-74-81?v=Novus+Biologicals
    Average 94 stars, based on 24 article reviews
    anti peroxisome proliferator activated receptor alpha - by Bioz Stars, 2026-07
    94/100 stars

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    Novus Biologicals ppar alpha
    PPARγ activation upregulates Lipin-1, SIRT1, and SRSF10 expression and alters Lipin-1 isoform splicing in 3T3-L1 adipocytes. ( A ) Relative mRNA expression of Lpin1 , Sirt1 , and Srsf10 following PPARγ activation by 5 μM RGZ on Day 8 of differentiation. ( B ) Protein expression of Lipin-1 in RGZ-treated cells compared with untreated controls. ( C ) mRNA expression of Lpin1a and Lpin1b isoforms in the same treatment group. Statistical significance was assessed by Student’s t -test for ( A , B ) and one-way ANOVA followed by Tukey’s post hoc test for ( C ), comparing treated groups to the untreated control. Data are presented as means ± SEM from three independent experiments. * p <  0.05; ** p <  0.01; *** p <  0.001; **** p <  0.0001; ns, not significant.
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    novus biologicals NB600-636
    PPARγ activation upregulates Lipin-1, SIRT1, and SRSF10 expression and alters Lipin-1 isoform splicing in 3T3-L1 adipocytes. ( A ) Relative mRNA expression of Lpin1 , Sirt1 , and Srsf10 following PPARγ activation by 5 μM RGZ on Day 8 of differentiation. ( B ) Protein expression of Lipin-1 in RGZ-treated cells compared with untreated controls. ( C ) mRNA expression of Lpin1a and Lpin1b isoforms in the same treatment group. Statistical significance was assessed by Student’s t -test for ( A , B ) and one-way ANOVA followed by Tukey’s post hoc test for ( C ), comparing treated groups to the untreated control. Data are presented as means ± SEM from three independent experiments. * p <  0.05; ** p <  0.01; *** p <  0.001; **** p <  0.0001; ns, not significant.
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    Novus Biologicals anti pparα antibody
    PPARγ activation upregulates Lipin-1, SIRT1, and SRSF10 expression and alters Lipin-1 isoform splicing in 3T3-L1 adipocytes. ( A ) Relative mRNA expression of Lpin1 , Sirt1 , and Srsf10 following PPARγ activation by 5 μM RGZ on Day 8 of differentiation. ( B ) Protein expression of Lipin-1 in RGZ-treated cells compared with untreated controls. ( C ) mRNA expression of Lpin1a and Lpin1b isoforms in the same treatment group. Statistical significance was assessed by Student’s t -test for ( A , B ) and one-way ANOVA followed by Tukey’s post hoc test for ( C ), comparing treated groups to the untreated control. Data are presented as means ± SEM from three independent experiments. * p <  0.05; ** p <  0.01; *** p <  0.001; **** p <  0.0001; ns, not significant.
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    Image Search Results


    PPARγ activation upregulates Lipin-1, SIRT1, and SRSF10 expression and alters Lipin-1 isoform splicing in 3T3-L1 adipocytes. ( A ) Relative mRNA expression of Lpin1 , Sirt1 , and Srsf10 following PPARγ activation by 5 μM RGZ on Day 8 of differentiation. ( B ) Protein expression of Lipin-1 in RGZ-treated cells compared with untreated controls. ( C ) mRNA expression of Lpin1a and Lpin1b isoforms in the same treatment group. Statistical significance was assessed by Student’s t -test for ( A , B ) and one-way ANOVA followed by Tukey’s post hoc test for ( C ), comparing treated groups to the untreated control. Data are presented as means ± SEM from three independent experiments. * p <  0.05; ** p <  0.01; *** p <  0.001; **** p <  0.0001; ns, not significant.

    Journal: Biomedicines

    Article Title: Lipin-1 Drives Browning of White Adipocytes via Promotion of Brown Phenotype Markers

    doi: 10.3390/biomedicines13092069

    Figure Lengend Snippet: PPARγ activation upregulates Lipin-1, SIRT1, and SRSF10 expression and alters Lipin-1 isoform splicing in 3T3-L1 adipocytes. ( A ) Relative mRNA expression of Lpin1 , Sirt1 , and Srsf10 following PPARγ activation by 5 μM RGZ on Day 8 of differentiation. ( B ) Protein expression of Lipin-1 in RGZ-treated cells compared with untreated controls. ( C ) mRNA expression of Lpin1a and Lpin1b isoforms in the same treatment group. Statistical significance was assessed by Student’s t -test for ( A , B ) and one-way ANOVA followed by Tukey’s post hoc test for ( C ), comparing treated groups to the untreated control. Data are presented as means ± SEM from three independent experiments. * p <  0.05; ** p <  0.01; *** p <  0.001; **** p <  0.0001; ns, not significant.

    Article Snippet: Protein detection was carried out using primary antibodies against Lipin-1 (Novus Biologicals, Centennial, CO, USA; Cat. No: NB110-57150), UCP1 (R&D Systems, Minneapolis, MN, USA; Cat. No: MAB-6158), PGC1 alpha (Novus Biologicals, Centennial, CO, USA; Cat. No: NBP1-04676), and PPAR alpha (Novus Biologicals, Centennial, CO, USA; Cat. No: NB600-636).

    Techniques: Activation Assay, Expressing, Control

    SIRT1 activation and brown adipocyte marker expression. ( A ) PPARα and ( B ) UCP1 protein levels appeared elevated in 3T3-L1 cells treated with SRT1720 during the differentiation period. Statistical significance was assessed by Student’s t -test, comparing treated groups to the untreated control. Data are presented as means ± SEM from three independent experiments. * p <  0.05; *** p <  0.001.

    Journal: Biomedicines

    Article Title: Lipin-1 Drives Browning of White Adipocytes via Promotion of Brown Phenotype Markers

    doi: 10.3390/biomedicines13092069

    Figure Lengend Snippet: SIRT1 activation and brown adipocyte marker expression. ( A ) PPARα and ( B ) UCP1 protein levels appeared elevated in 3T3-L1 cells treated with SRT1720 during the differentiation period. Statistical significance was assessed by Student’s t -test, comparing treated groups to the untreated control. Data are presented as means ± SEM from three independent experiments. * p <  0.05; *** p <  0.001.

    Article Snippet: Protein detection was carried out using primary antibodies against Lipin-1 (Novus Biologicals, Centennial, CO, USA; Cat. No: NB110-57150), UCP1 (R&D Systems, Minneapolis, MN, USA; Cat. No: MAB-6158), PGC1 alpha (Novus Biologicals, Centennial, CO, USA; Cat. No: NBP1-04676), and PPAR alpha (Novus Biologicals, Centennial, CO, USA; Cat. No: NB600-636).

    Techniques: Activation Assay, Marker, Expressing, Control