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ppar γ rabbit  (Proteintech)


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    Structured Review

    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.
    Ppar γ Rabbit, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 562 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ppar γ rabbit/product/Proteintech
    Average 96 stars, based on 562 article reviews
    ppar γ rabbit - by Bioz Stars, 2026-03
    96/100 stars

    Images

    1) Product Images from "Citri grandis Exocarpium Extract Alleviates Atherosclerosis in ApoE −/− Mice by Modulating the Expression of TGF-β1, PI3K, AKT1, PPAR-γ, LXR-α, and ABCA1"

    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

    Journal: Foods

    doi: 10.3390/foods14244267

    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.
    Figure Legend 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.

    Techniques Used: 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.
    Figure Legend 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.

    Techniques Used: Expressing, Control



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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