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rabbit anti ppar gamma polyclonal antibody  (Bioss)


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    Structured Review

    Bioss rabbit anti ppar gamma polyclonal antibody
    Rabbit Anti Ppar Gamma Polyclonal Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 71 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+ppar+gamma+polyclonal+antibody/PPAR+gamma+Polyclonal+Antibody/pmc13158677-61-5-11
    Average 94 stars, based on 71 article reviews
    rabbit anti ppar gamma polyclonal antibody - by Bioz Stars, 2026-11
    94/100 stars

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    Related Articles

    other:

    Article Title: RIN2 reveals a novel role in regulating proliferation and early adipogenesis of chicken preadipocytes
    Article Snippet: The following antibodies were used: Rabbit Anti-PPAR gamma Polyclonal Antibody (bs-0530R, Bioss, China, 1:1,000), Rabbit Anti-CEBP alpha Polyclonal Antibody (bs-24540R, Bioss, China, 1:1,000), Rabbit Anti-CEBP beta Polyclonal Antibody (bs-1396R, Bioss, China, 1:1,000), Rabbit Anti-Cyclin D2 Polyclonal Antibody (AF5410, Affinity, China, 1:1,000), Rabbit Anti-CDKN1B/p27 KIP 1 Polyclonal Antibody (bs-0742R, Bioss, China, 1:1,000), β-Actin Mouse Monoclonal Antibody (AF0003, Beyotime, China,1:10,000), and HRP-labeled Goat Anti-Rabbit IgG H+L (A0208, Beyotime, China, 1:10,000) were used as a secondary antibody.

    Western Blot:

    Article Title: Growth Hormone Receptor Controls Adipogenic Differentiation of Chicken Bone Marrow Mesenchymal Stem Cells by Affecting Mitochondrial Biogenesis and Mitochondrial Function
    Article Snippet: .. The following antibodies and their dilutions were used in western blot: mouse anti-PGC1 alpha antibody (1C1B2, 1:5,000; Proteintech, Rosemont, United States), rabbit anti-NRF1 antibody (AF7620, 1:1,000; Beyotime), rabbit anti-TOMM20 antibody (AF1717, 1:1,000; Beyotime), rabbit anti-PPAR gamma polyclonal antibody (bs-0530R, 1:1,000; Bioss, Beijing, China), rabbit anti-CEBP alpha polyclonal antibody (bs-24540R, 1:1,000; Bioss), rabbit anti-beta-actin antibody (bs-0061R, 1:5,000; Bioss), goat anti-rabbit IgG-HRP (BS13278, 1:10,000; Bioworld, Minnesota, United States), and goat anti-mouse IgG-HRP (BS12478, 1:10,000; Bioworld). ..

    Article Title: Growth hormone receptor controls adipogenic differentiation of chicken bone marrow mesenchymal stem cells by affecting mitochondrial function
    Article Snippet: .. Page 9/25 The following antibodies and their dilutions were used in western blot: mouse anti-PGC1 alpha antibody (1C1B2, 1:5,000; Proteintech, Rosemont, USA), rabbit anti-NRF1 antibody (AF7620, 1:1,000; Beyotime), rabbit anti-TOMM20 antibody (AF1717, 1:1,000; Beyotime), rabbit anti-PPAR gamma polyclonal antibody (bs-0530R, 1:1,000; Bioss, Beijing, China), rabbit anti-CEBP alpha polyclonal antibody (bs-24540R, 1:1,000; Bioss), rabbit anti-beta-actin antibody (bs-0061R, 1:5,000; Bioss), goat anti-rabbit IgG-HRP (BS13278, 1:10,000; Bioworld, Minnesota, USA), and goat anti-mouse IgG-HRP (BS12478, 1:10,000; Bioworld). ..

    Article Title: Myogenic Determination and Differentiation of Chicken Bone Marrow-Derived Mesenchymal Stem Cells under Different Inductive Agents
    Article Snippet: .. The following antibodies and their dilutions were used in the Western blot: rabbit anti-PPAR gamma polyclonal antibody (bs0530R, Bioss, Zhuhai, China, 1:1000); rabbit anti-CEBP alpha polyclonal antibody (bs-24540R, Bioss, Zhuhai, China, 1:1000); rabbit anti-beta-actin polyclonal antibody (bs-0061R, Bioss, Zhuhai, China, 1:5000); MyoD1 monoclonal antibody (PM2147a, GenePharma, Suzhou, China, 1:100); MyoG polyclonal antibody (orb6492, Biorbyt, Cambridge, UK, 1:500); HRP, Goat Anti-Rabbit IgG polyclonal (A21020, Abbkine, Wuhan, China, 1:10,000); and HRP, Goat Anti-Mouse IgG polyclonal (A21010, Abbkine, Wuhan, China, 1:10,000). .. Total RNA extraction and cDNA synthesis followed the method described above. cDNA samples were subjected to ChamQ Universal SYBR qPCR Master Mix (Vazyme Biotech, Nanjing, China) following the manufacturer’s protocol.

    Article Title: ALDH1A1 Inhibits Chicken Preadipocytes’ Proliferation and Differentiation via the PPARγ Pathway In Vitro and In Vivo
    Article Snippet: .. The antibodies and their dilutions used for Western blots were as follows: Rabbit Anti-ALDH1A1 antibody (GTX123973; GeneTex, San Antonio, TX, USA; 1:5000), Rabbit Anti-CEBP Beta Polyclonal Antibody (bs-1396R; Bioss, Beijing, China; 1:500) [ , ], Rabbit Anti-PPAR Gamma Polyclonal Antibody (bs-0530R; Bioss, China; 1:500), Rabbit Anti-Adiponectin Polyclonal Antibody (bs-0471R; Bioss, Beijing, China; 1:500) [ ], Rabbit Anti-GAPDH (AB-P-R 001; Hangzhou Goodhere Biotechnology Co. Ltd., Hangzhou, China; 1:10,000), Goat Anti-rabbit IgG-HRP(BA1054; Boster, Wuhan, China; 1:10,000), and Peroxidase-goat Anti-mouse IgG (BA1051; Boster, Wuhan, China; 1:10,000). ..



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    Proteintech ppar γ rabbit
    Representative blotting images and protein densitometry showing the relative expression levels of TGF-β, PI3K, AKT1, <t>PPAR-γ,</t> LXR-α, and ABCA1 proteins normalized with GAPDH and β-actin in aorta of apoE −/− mice . ( A , E ) are the representative protein blotting images; ( B – D , F – H ) Expression levels of TGF-β, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1 proteins in aorta were shown in the bar chart and the blotting grayscale value analyses normalized with GAPDH and β-actin (Wilks’ Λ = 0.003, R 2 = 0.970, Eta 2 = 0.970), which were used as loading control. The error bars represented x ¯ ± SE. * p < 0.05, ** p < 0.01, and *** p < 0.001 vs. the MOD group indicate a statistically significant difference; n = at least 3 for each group.
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    Representative blotting images and protein densitometry showing the relative expression levels of TGF-β, PI3K, AKT1, <t>PPAR-γ,</t> LXR-α, and ABCA1 proteins normalized with GAPDH and β-actin in aorta of apoE −/− mice . ( A , E ) are the representative protein blotting images; ( B – D , F – H ) Expression levels of TGF-β, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1 proteins in aorta were shown in the bar chart and the blotting grayscale value analyses normalized with GAPDH and β-actin (Wilks’ Λ = 0.003, R 2 = 0.970, Eta 2 = 0.970), which were used as loading control. The error bars represented x ¯ ± SE. * p < 0.05, ** p < 0.01, and *** p < 0.001 vs. the MOD group indicate a statistically significant difference; n = at least 3 for each group.
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    Image Search Results


    Representative blotting images and protein densitometry showing the relative expression levels of TGF-β, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1 proteins normalized with GAPDH and β-actin in aorta of apoE −/− mice . ( A , E ) are the representative protein blotting images; ( B – D , F – H ) Expression levels of TGF-β, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1 proteins in aorta were shown in the bar chart and the blotting grayscale value analyses normalized with GAPDH and β-actin (Wilks’ Λ = 0.003, R 2 = 0.970, Eta 2 = 0.970), which were used as loading control. The error bars represented x ¯ ± SE. * p < 0.05, ** p < 0.01, and *** p < 0.001 vs. the MOD group indicate a statistically significant difference; n = at least 3 for each group.

    Journal: Foods

    Article Title: Citri grandis Exocarpium Extract Alleviates Atherosclerosis in ApoE −/− Mice by Modulating the Expression of TGF-β1, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1

    doi: 10.3390/foods14244267

    Figure Lengend Snippet: Representative blotting images and protein densitometry showing the relative expression levels of TGF-β, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1 proteins normalized with GAPDH and β-actin in aorta of apoE −/− mice . ( A , E ) are the representative protein blotting images; ( B – D , F – H ) Expression levels of TGF-β, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1 proteins in aorta were shown in the bar chart and the blotting grayscale value analyses normalized with GAPDH and β-actin (Wilks’ Λ = 0.003, R 2 = 0.970, Eta 2 = 0.970), which were used as loading control. The error bars represented x ¯ ± SE. * p < 0.05, ** p < 0.01, and *** p < 0.001 vs. the MOD group indicate a statistically significant difference; n = at least 3 for each group.

    Article Snippet: Polyclonal antibodies for AKT1 (rabbit), PPAR-γ (rabbit), LXR-α (rabbit), and ABCA1 (rabbit) were obtained from Proteintech (Wuhan, China).

    Techniques: Expressing, Control

    Effect of CGE on the expression of TGF-β, PI3K, AKT, PPAR-γ, LXR-α, and ABCA1 in mouse livers . ( A – F ) represent the mRNA expression levels of TGF-β, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1 to GAPDH in livers, respectively (Wilks’ Λ = 0.001, R 2 = 0.953, Eta 2 = 0.958). ( G , K ) are the representative protein blotting images; ( H – J , L – N ) are the respective optical density ratios of bands, which represent the relative expression levels of TGF-β, PI3K, AKT, PPAR-γ, LXR-α, and ABCA1 proteins normalized with GAPDH or β-actin in the livers of apoE −/− mice (Wilks’ Λ = 0.008, R 2 = 0.986, Eta 2 = 0.986). The blotting grayscale value was analyzed relative to the GAPDH band and β-actin, as a loading control. The error bars represent the x ¯ ± SE. It is considered to have statistically significant differences when * p < 0.05, ** p < 0.01, and *** p < 0.001 vs. the MOD group; n = at least 3 for each group.

    Journal: Foods

    Article Title: Citri grandis Exocarpium Extract Alleviates Atherosclerosis in ApoE −/− Mice by Modulating the Expression of TGF-β1, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1

    doi: 10.3390/foods14244267

    Figure Lengend Snippet: Effect of CGE on the expression of TGF-β, PI3K, AKT, PPAR-γ, LXR-α, and ABCA1 in mouse livers . ( A – F ) represent the mRNA expression levels of TGF-β, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1 to GAPDH in livers, respectively (Wilks’ Λ = 0.001, R 2 = 0.953, Eta 2 = 0.958). ( G , K ) are the representative protein blotting images; ( H – J , L – N ) are the respective optical density ratios of bands, which represent the relative expression levels of TGF-β, PI3K, AKT, PPAR-γ, LXR-α, and ABCA1 proteins normalized with GAPDH or β-actin in the livers of apoE −/− mice (Wilks’ Λ = 0.008, R 2 = 0.986, Eta 2 = 0.986). The blotting grayscale value was analyzed relative to the GAPDH band and β-actin, as a loading control. The error bars represent the x ¯ ± SE. It is considered to have statistically significant differences when * p < 0.05, ** p < 0.01, and *** p < 0.001 vs. the MOD group; n = at least 3 for each group.

    Article Snippet: Polyclonal antibodies for AKT1 (rabbit), PPAR-γ (rabbit), LXR-α (rabbit), and ABCA1 (rabbit) were obtained from Proteintech (Wuhan, China).

    Techniques: Expressing, Control