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rabbit polyclonal fatp1 primary antibody  (Novus Biologicals)


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    Novus Biologicals rabbit polyclonal fatp1 primary antibody
    Fig. 3 Effect of low temperature on gene expression and lipid accumu lation in cultured human proximal tubular cells. (a–c) Comparison of gene expression in HK2 cells cultured at 37 °C and 28 °C, as analyzed by real-time RT-PCR for (a) SLC27A1 mRNA, (b) PPARA mRNA, and CD36 mRNA (n = 6 per condition). (c) Western blot analysis of <t>FATP1</t> and β-actin proteins in HK2 cells cultured at 37 °C and 28 °C, with quantitative data derived from western blotting (n = 6 per condition). (d) Analysis of lipid accumulation in HK2 cells cultured at 37 °C and 28 °C with 0.1 mM palmitic acid (PA) and/ or a FATP1 inhibitor. Lipids are visualized using BODIPY (green), with nuclei counterstained with DAPI (blue). Scale bars: 10 μm. (e) Quantitative analysis of fluores cence intensity representing lipid accumulation in HK2 cells cultured at 37 °C and 28 °C (n = 12 per con dition). Data were analyzed using one-way ANOVA followed by the Mann–Whitney U test. All data are presented as mean ± SEM. *P < 0.05, ****P < 0.0001
    Rabbit Polyclonal Fatp1 Primary Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal fatp1 primary antibody/product/Novus Biologicals
    Average 93 stars, based on 2 article reviews
    rabbit polyclonal fatp1 primary antibody - by Bioz Stars, 2026-06
    93/100 stars

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    1) Product Images from "Hypothermia drives fatty acid transporter 1 upregulation and lipid accumulation in renal tubules: evidence from forensic cases."

    Article Title: Hypothermia drives fatty acid transporter 1 upregulation and lipid accumulation in renal tubules: evidence from forensic cases.

    Journal: International journal of legal medicine

    doi: 10.1007/s00414-025-03550-x

    Fig. 3 Effect of low temperature on gene expression and lipid accumu lation in cultured human proximal tubular cells. (a–c) Comparison of gene expression in HK2 cells cultured at 37 °C and 28 °C, as analyzed by real-time RT-PCR for (a) SLC27A1 mRNA, (b) PPARA mRNA, and CD36 mRNA (n = 6 per condition). (c) Western blot analysis of FATP1 and β-actin proteins in HK2 cells cultured at 37 °C and 28 °C, with quantitative data derived from western blotting (n = 6 per condition). (d) Analysis of lipid accumulation in HK2 cells cultured at 37 °C and 28 °C with 0.1 mM palmitic acid (PA) and/ or a FATP1 inhibitor. Lipids are visualized using BODIPY (green), with nuclei counterstained with DAPI (blue). Scale bars: 10 μm. (e) Quantitative analysis of fluores cence intensity representing lipid accumulation in HK2 cells cultured at 37 °C and 28 °C (n = 12 per con dition). Data were analyzed using one-way ANOVA followed by the Mann–Whitney U test. All data are presented as mean ± SEM. *P < 0.05, ****P < 0.0001
    Figure Legend Snippet: Fig. 3 Effect of low temperature on gene expression and lipid accumu lation in cultured human proximal tubular cells. (a–c) Comparison of gene expression in HK2 cells cultured at 37 °C and 28 °C, as analyzed by real-time RT-PCR for (a) SLC27A1 mRNA, (b) PPARA mRNA, and CD36 mRNA (n = 6 per condition). (c) Western blot analysis of FATP1 and β-actin proteins in HK2 cells cultured at 37 °C and 28 °C, with quantitative data derived from western blotting (n = 6 per condition). (d) Analysis of lipid accumulation in HK2 cells cultured at 37 °C and 28 °C with 0.1 mM palmitic acid (PA) and/ or a FATP1 inhibitor. Lipids are visualized using BODIPY (green), with nuclei counterstained with DAPI (blue). Scale bars: 10 μm. (e) Quantitative analysis of fluores cence intensity representing lipid accumulation in HK2 cells cultured at 37 °C and 28 °C (n = 12 per con dition). Data were analyzed using one-way ANOVA followed by the Mann–Whitney U test. All data are presented as mean ± SEM. *P < 0.05, ****P < 0.0001

    Techniques Used: Gene Expression, Cell Culture, Comparison, Quantitative RT-PCR, Western Blot, Derivative Assay, MANN-WHITNEY



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    rabbit polyclonal fatp1 primary antibody  (Novus Biologicals)
    93
    Novus Biologicals rabbit polyclonal fatp1 primary antibody
    Fig. 3 Effect of low temperature on gene expression and lipid accumu lation in cultured human proximal tubular cells. (a–c) Comparison of gene expression in HK2 cells cultured at 37 °C and 28 °C, as analyzed by real-time RT-PCR for (a) SLC27A1 mRNA, (b) PPARA mRNA, and CD36 mRNA (n = 6 per condition). (c) Western blot analysis of <t>FATP1</t> and β-actin proteins in HK2 cells cultured at 37 °C and 28 °C, with quantitative data derived from western blotting (n = 6 per condition). (d) Analysis of lipid accumulation in HK2 cells cultured at 37 °C and 28 °C with 0.1 mM palmitic acid (PA) and/ or a FATP1 inhibitor. Lipids are visualized using BODIPY (green), with nuclei counterstained with DAPI (blue). Scale bars: 10 μm. (e) Quantitative analysis of fluores cence intensity representing lipid accumulation in HK2 cells cultured at 37 °C and 28 °C (n = 12 per con dition). Data were analyzed using one-way ANOVA followed by the Mann–Whitney U test. All data are presented as mean ± SEM. *P < 0.05, ****P < 0.0001
    Rabbit Polyclonal Fatp1 Primary Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal fatp1 primary antibody/product/Novus Biologicals
    Average 93 stars, based on 1 article reviews
    rabbit polyclonal fatp1 primary antibody - by Bioz Stars, 2026-06
    93/100 stars
    		  Buy from Supplier

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    Fig. 3 Effect of low temperature on gene expression and lipid accumu lation in cultured human proximal tubular cells. (a–c) Comparison of gene expression in HK2 cells cultured at 37 °C and 28 °C, as analyzed by real-time RT-PCR for (a) SLC27A1 mRNA, (b) PPARA mRNA, and CD36 mRNA (n = 6 per condition). (c) Western blot analysis of FATP1 and β-actin proteins in HK2 cells cultured at 37 °C and 28 °C, with quantitative data derived from western blotting (n = 6 per condition). (d) Analysis of lipid accumulation in HK2 cells cultured at 37 °C and 28 °C with 0.1 mM palmitic acid (PA) and/ or a FATP1 inhibitor. Lipids are visualized using BODIPY (green), with nuclei counterstained with DAPI (blue). Scale bars: 10 μm. (e) Quantitative analysis of fluores cence intensity representing lipid accumulation in HK2 cells cultured at 37 °C and 28 °C (n = 12 per con dition). Data were analyzed using one-way ANOVA followed by the Mann–Whitney U test. All data are presented as mean ± SEM. *P < 0.05, ****P < 0.0001

    Journal: International journal of legal medicine

    Article Title: Hypothermia drives fatty acid transporter 1 upregulation and lipid accumulation in renal tubules: evidence from forensic cases.

    doi: 10.1007/s00414-025-03550-x

    Figure Lengend Snippet: Fig. 3 Effect of low temperature on gene expression and lipid accumu lation in cultured human proximal tubular cells. (a–c) Comparison of gene expression in HK2 cells cultured at 37 °C and 28 °C, as analyzed by real-time RT-PCR for (a) SLC27A1 mRNA, (b) PPARA mRNA, and CD36 mRNA (n = 6 per condition). (c) Western blot analysis of FATP1 and β-actin proteins in HK2 cells cultured at 37 °C and 28 °C, with quantitative data derived from western blotting (n = 6 per condition). (d) Analysis of lipid accumulation in HK2 cells cultured at 37 °C and 28 °C with 0.1 mM palmitic acid (PA) and/ or a FATP1 inhibitor. Lipids are visualized using BODIPY (green), with nuclei counterstained with DAPI (blue). Scale bars: 10 μm. (e) Quantitative analysis of fluores cence intensity representing lipid accumulation in HK2 cells cultured at 37 °C and 28 °C (n = 12 per con dition). Data were analyzed using one-way ANOVA followed by the Mann–Whitney U test. All data are presented as mean ± SEM. *P < 0.05, ****P < 0.0001

    Article Snippet: Sections were then incubated with a rabbit polyclonal FATP1 primary antibody (Novus Biologicals, Littleton, CO, USA), followed by detection with a horseradish peroxidase (HRP)-conjugated secondary rabbit IgG antibody (Vector Labs, Burlingame, CA, USA).

    Techniques: Gene Expression, Cell Culture, Comparison, Quantitative RT-PCR, Western Blot, Derivative Assay, MANN-WHITNEY