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recombinant human angptl4 protein  (MedChemExpress)


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    MedChemExpress recombinant human angptl4 protein
    Recombinant Human Angptl4 Protein, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 63 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/recombinant human angptl4 protein/product/MedChemExpress
    Average 95 stars, based on 63 article reviews
    recombinant human angptl4 protein - by Bioz Stars, 2026-02
    95/100 stars

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    FIGURE 5 Lipolysis products induce the expression of <t>Angptl4</t> in MC3T3‐E1 cells. Cells were exposed to 0−150 mg/dL TGRL mixed with 2 units/mL LPL for 3 or 6 h. Bars represent mean ± SEM, n = 4−6, ****p < 0.0001 compared to 0 TGRL + LPL (Ctrl). LPL, lipoprotein lipase; TGRL, triglyceride‐rich lipoproteins.
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    FIGURE 5 Lipolysis products induce the expression of <t>Angptl4</t> in MC3T3‐E1 cells. Cells were exposed to 0−150 mg/dL TGRL mixed with 2 units/mL LPL for 3 or 6 h. Bars represent mean ± SEM, n = 4−6, ****p < 0.0001 compared to 0 TGRL + LPL (Ctrl). LPL, lipoprotein lipase; TGRL, triglyceride‐rich lipoproteins.
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    FIGURE 5 Lipolysis products induce the expression of <t>Angptl4</t> in MC3T3‐E1 cells. Cells were exposed to 0−150 mg/dL TGRL mixed with 2 units/mL LPL for 3 or 6 h. Bars represent mean ± SEM, n = 4−6, ****p < 0.0001 compared to 0 TGRL + LPL (Ctrl). LPL, lipoprotein lipase; TGRL, triglyceride‐rich lipoproteins.
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    FIGURE 5 Lipolysis products induce the expression of <t>Angptl4</t> in MC3T3‐E1 cells. Cells were exposed to 0−150 mg/dL TGRL mixed with 2 units/mL LPL for 3 or 6 h. Bars represent mean ± SEM, n = 4−6, ****p < 0.0001 compared to 0 TGRL + LPL (Ctrl). LPL, lipoprotein lipase; TGRL, triglyceride‐rich lipoproteins.
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    Fig. 7. Integrated analysis of publicly-available murine single cell RNA-sequencing (scRNA-seq) data and in vitro treatment with recombinant <t>ANGPTL4</t> protein. (a) Integrated analysis of murine skeletal muscle scRNA-seq data, clustering of cell types, and analysis of cell–cell communication networks. (b) and (d), EdU staining of porcine MuSCs and C2C12 cells. The S-phase is stained with EdU (green), and the nuclei are stained with Hoechst 33342 (blue). (c) and (e), Immunofluorescence staining of MyHc. Porcine myofibers are stained green, and nuclei are stained blue. Abbreviations: ANGPTL4, angiopoietin like4; EdU, 5-ethynyl-20-deoxyuridine; MyHc, myosin heavy chain; FAPs, fibro-adipogenic progenitors.
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    Fig. 7. Integrated analysis of publicly-available murine single cell RNA-sequencing (scRNA-seq) data and in vitro treatment with recombinant <t>ANGPTL4</t> protein. (a) Integrated analysis of murine skeletal muscle scRNA-seq data, clustering of cell types, and analysis of cell–cell communication networks. (b) and (d), EdU staining of porcine MuSCs and C2C12 cells. The S-phase is stained with EdU (green), and the nuclei are stained with Hoechst 33342 (blue). (c) and (e), Immunofluorescence staining of MyHc. Porcine myofibers are stained green, and nuclei are stained blue. Abbreviations: ANGPTL4, angiopoietin like4; EdU, 5-ethynyl-20-deoxyuridine; MyHc, myosin heavy chain; FAPs, fibro-adipogenic progenitors.
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    Fig. 7. Integrated analysis of publicly-available murine single cell RNA-sequencing (scRNA-seq) data and in vitro treatment with recombinant <t>ANGPTL4</t> protein. (a) Integrated analysis of murine skeletal muscle scRNA-seq data, clustering of cell types, and analysis of cell–cell communication networks. (b) and (d), EdU staining of porcine MuSCs and C2C12 cells. The S-phase is stained with EdU (green), and the nuclei are stained with Hoechst 33342 (blue). (c) and (e), Immunofluorescence staining of MyHc. Porcine myofibers are stained green, and nuclei are stained blue. Abbreviations: ANGPTL4, angiopoietin like4; EdU, 5-ethynyl-20-deoxyuridine; MyHc, myosin heavy chain; FAPs, fibro-adipogenic progenitors.
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    Fig. 7. Integrated analysis of publicly-available murine single cell RNA-sequencing (scRNA-seq) data and in vitro treatment with recombinant <t>ANGPTL4</t> protein. (a) Integrated analysis of murine skeletal muscle scRNA-seq data, clustering of cell types, and analysis of cell–cell communication networks. (b) and (d), EdU staining of porcine MuSCs and C2C12 cells. The S-phase is stained with EdU (green), and the nuclei are stained with Hoechst 33342 (blue). (c) and (e), Immunofluorescence staining of MyHc. Porcine myofibers are stained green, and nuclei are stained blue. Abbreviations: ANGPTL4, angiopoietin like4; EdU, 5-ethynyl-20-deoxyuridine; MyHc, myosin heavy chain; FAPs, fibro-adipogenic progenitors.
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    FIGURE 5 Lipolysis products induce the expression of Angptl4 in MC3T3‐E1 cells. Cells were exposed to 0−150 mg/dL TGRL mixed with 2 units/mL LPL for 3 or 6 h. Bars represent mean ± SEM, n = 4−6, ****p < 0.0001 compared to 0 TGRL + LPL (Ctrl). LPL, lipoprotein lipase; TGRL, triglyceride‐rich lipoproteins.

    Journal: Journal of orthopaedic research : official publication of the Orthopaedic Research Society

    Article Title: Lipolysis products from triglyceride-rich lipoproteins induce stress protein ATF3 in osteoblasts.

    doi: 10.1002/jor.25756

    Figure Lengend Snippet: FIGURE 5 Lipolysis products induce the expression of Angptl4 in MC3T3‐E1 cells. Cells were exposed to 0−150 mg/dL TGRL mixed with 2 units/mL LPL for 3 or 6 h. Bars represent mean ± SEM, n = 4−6, ****p < 0.0001 compared to 0 TGRL + LPL (Ctrl). LPL, lipoprotein lipase; TGRL, triglyceride‐rich lipoproteins.

    Article Snippet: Recombinant full length murine ANGPTL4 (4880‐AN‐050) was purchased from R&D Systems.

    Techniques: Expressing

    FIGURE 6 Recombinant ANGPTL4 inhibits lipolysis product‐ induction of Atf3 in MC3T3‐E1 cells. Cells were exposed to 100 mg/dL TGRL mixed with 2 units/mL LPL for 6 h. In some experiments, LPL and ANGPTL4 (0.1−5 µg/mL) were mixed for 30 min before the addition of TGRL. Ctrl represents cells not exposed to TGRL/LPL/ANGPTL4. Bars represent mean ± SEM, n = 4−6. *p < 0.05, ***p < 0.001, ****p < 0.0001 compared to 0 µg/mL ANGPTL4. LPL, lipoprotein lipase; TGRL, triglyceride‐rich lipoproteins.

    Journal: Journal of orthopaedic research : official publication of the Orthopaedic Research Society

    Article Title: Lipolysis products from triglyceride-rich lipoproteins induce stress protein ATF3 in osteoblasts.

    doi: 10.1002/jor.25756

    Figure Lengend Snippet: FIGURE 6 Recombinant ANGPTL4 inhibits lipolysis product‐ induction of Atf3 in MC3T3‐E1 cells. Cells were exposed to 100 mg/dL TGRL mixed with 2 units/mL LPL for 6 h. In some experiments, LPL and ANGPTL4 (0.1−5 µg/mL) were mixed for 30 min before the addition of TGRL. Ctrl represents cells not exposed to TGRL/LPL/ANGPTL4. Bars represent mean ± SEM, n = 4−6. *p < 0.05, ***p < 0.001, ****p < 0.0001 compared to 0 µg/mL ANGPTL4. LPL, lipoprotein lipase; TGRL, triglyceride‐rich lipoproteins.

    Article Snippet: Recombinant full length murine ANGPTL4 (4880‐AN‐050) was purchased from R&D Systems.

    Techniques: Recombinant

    FIGURE 11 (A) Lipoprotein lipase (LPL) (or hepatic lipase) secreted by the osteoblast translocates to the plasma membrane of endothelial cells lining blood vessels, where it catalyzes the conversion of triglyceride‐rich lipoproteins (TGRL) into lipolysis products (LP) such as free fatty acids (FFA). LP translocate to the osteoblast for use as a metabolic fuel source. (B) High circulating levels of TGRL result in high levels of LP which induce an increase in ATF3 in osteoblasts (pathway 1), and induce IL6 and COX‐2, known downstream genes of ATF3; LP also induce intracellular ROS accumulation, which together result in inflammation. LP induce an increase in angiopoietin‐like 4 (ANGPTL4) (pathway 2), an inhibitor of LPL, which may act in a negative feedback loop, reducing LPL activity, reducing LP accumulation in the local environment, and protecting cells from inflammation. Note it is possible that lipases may be active on the osteoblast cell membrane itself. ATF3, activating transcription factor 3; ROS, reactive oxygen species.

    Journal: Journal of orthopaedic research : official publication of the Orthopaedic Research Society

    Article Title: Lipolysis products from triglyceride-rich lipoproteins induce stress protein ATF3 in osteoblasts.

    doi: 10.1002/jor.25756

    Figure Lengend Snippet: FIGURE 11 (A) Lipoprotein lipase (LPL) (or hepatic lipase) secreted by the osteoblast translocates to the plasma membrane of endothelial cells lining blood vessels, where it catalyzes the conversion of triglyceride‐rich lipoproteins (TGRL) into lipolysis products (LP) such as free fatty acids (FFA). LP translocate to the osteoblast for use as a metabolic fuel source. (B) High circulating levels of TGRL result in high levels of LP which induce an increase in ATF3 in osteoblasts (pathway 1), and induce IL6 and COX‐2, known downstream genes of ATF3; LP also induce intracellular ROS accumulation, which together result in inflammation. LP induce an increase in angiopoietin‐like 4 (ANGPTL4) (pathway 2), an inhibitor of LPL, which may act in a negative feedback loop, reducing LPL activity, reducing LP accumulation in the local environment, and protecting cells from inflammation. Note it is possible that lipases may be active on the osteoblast cell membrane itself. ATF3, activating transcription factor 3; ROS, reactive oxygen species.

    Article Snippet: Recombinant full length murine ANGPTL4 (4880‐AN‐050) was purchased from R&D Systems.

    Techniques: Clinical Proteomics, Membrane, Activity Assay

    Fig. 7. Integrated analysis of publicly-available murine single cell RNA-sequencing (scRNA-seq) data and in vitro treatment with recombinant ANGPTL4 protein. (a) Integrated analysis of murine skeletal muscle scRNA-seq data, clustering of cell types, and analysis of cell–cell communication networks. (b) and (d), EdU staining of porcine MuSCs and C2C12 cells. The S-phase is stained with EdU (green), and the nuclei are stained with Hoechst 33342 (blue). (c) and (e), Immunofluorescence staining of MyHc. Porcine myofibers are stained green, and nuclei are stained blue. Abbreviations: ANGPTL4, angiopoietin like4; EdU, 5-ethynyl-20-deoxyuridine; MyHc, myosin heavy chain; FAPs, fibro-adipogenic progenitors.

    Journal: Agriculture Communications

    Article Title: Single-cell transcriptional profiling of porcine muscle satellite cells and myoblasts during myogenesis

    doi: 10.1016/j.agrcom.2024.100026

    Figure Lengend Snippet: Fig. 7. Integrated analysis of publicly-available murine single cell RNA-sequencing (scRNA-seq) data and in vitro treatment with recombinant ANGPTL4 protein. (a) Integrated analysis of murine skeletal muscle scRNA-seq data, clustering of cell types, and analysis of cell–cell communication networks. (b) and (d), EdU staining of porcine MuSCs and C2C12 cells. The S-phase is stained with EdU (green), and the nuclei are stained with Hoechst 33342 (blue). (c) and (e), Immunofluorescence staining of MyHc. Porcine myofibers are stained green, and nuclei are stained blue. Abbreviations: ANGPTL4, angiopoietin like4; EdU, 5-ethynyl-20-deoxyuridine; MyHc, myosin heavy chain; FAPs, fibro-adipogenic progenitors.

    Article Snippet: Briefly, MuSCs were seeded into 96-well plates and treated with DMEM/F-12 proliferation medium containing 2.5 μg/mL recombinant ANGPTL4 protein (CUSABIO, Wuhan, China) for two days [17].

    Techniques: RNA Sequencing, In Vitro, Recombinant, Staining