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beclin1 rabbit polyclonal antibody  (Proteintech)


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    Proteintech beclin1 rabbit polyclonal antibody
    Beclin1 Rabbit Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1517 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/beclin1+rabbit+polyclonal+antibody/Beclin+1+Antibody/pm40768807-101-30-34
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    beclin1 rabbit polyclonal antibody - by Bioz Stars, 2026-10
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    Related Articles

    Membrane:

    Article Title: Haizao-Gancao herb pair ameliorates propylthiouracil-induced goiter by regulating the Beclin1-mediated autophagy.
    Article Snippet: Ethnopharmacological relevance: Haizao, Sargassum, is widely used to treat goiter.. Gancao, Glycyrrhizae radix et rhizome, is renowned for reducing toxicity or increasing effects in traditional Chinese medicine.. As a classic herb pair, Haizao–Gancao (HG) is a commonly used and effective combined therapy for goiter.

    Incubation:

    Article Title: Haizao-Gancao herb pair ameliorates propylthiouracil-induced goiter by regulating the Beclin1-mediated autophagy.
    Article Snippet: Ethnopharmacological relevance: Haizao, Sargassum, is widely used to treat goiter.. Gancao, Glycyrrhizae radix et rhizome, is renowned for reducing toxicity or increasing effects in traditional Chinese medicine.. As a classic herb pair, Haizao–Gancao (HG) is a commonly used and effective combined therapy for goiter.

    Article Title: Activated mTORC1 signaling pathway aggravates cisplatin induced oxidative damage by inhibiting autophagy in mouse cochlear hair cells.
    Article Snippet: Platinum-based antitumor drugs, such as cisplatin and carboplatin, are well-known for their severe ototoxicity.. The ototoxic effects of these drugs are primarily attributed to oxidative stress induced damage within cochlear hair cells (HCs), leading to cell death and subsequent irreversible hearing loss.. Over the past decade, studies have demonstrated that upregulating autophagy levels in HCs can greatly alleviate the death of cochlear HCs as part of the oxidative damage induced by ototoxic drugs.

    Blocking Assay:

    Article Title: Activated mTORC1 signaling pathway aggravates cisplatin induced oxidative damage by inhibiting autophagy in mouse cochlear hair cells.
    Article Snippet: Platinum-based antitumor drugs, such as cisplatin and carboplatin, are well-known for their severe ototoxicity.. The ototoxic effects of these drugs are primarily attributed to oxidative stress induced damage within cochlear hair cells (HCs), leading to cell death and subsequent irreversible hearing loss.. Over the past decade, studies have demonstrated that upregulating autophagy levels in HCs can greatly alleviate the death of cochlear HCs as part of the oxidative damage induced by ototoxic drugs.

    Phospho-proteomics:

    Article Title: Activated mTORC1 signaling pathway aggravates cisplatin induced oxidative damage by inhibiting autophagy in mouse cochlear hair cells.
    Article Snippet: Platinum-based antitumor drugs, such as cisplatin and carboplatin, are well-known for their severe ototoxicity.. The ototoxic effects of these drugs are primarily attributed to oxidative stress induced damage within cochlear hair cells (HCs), leading to cell death and subsequent irreversible hearing loss.. Over the past decade, studies have demonstrated that upregulating autophagy levels in HCs can greatly alleviate the death of cochlear HCs as part of the oxidative damage induced by ototoxic drugs.

    Western Blot:

    Article Title: Activated mTORC1 signaling pathway aggravates cisplatin induced oxidative damage by inhibiting autophagy in mouse cochlear hair cells.
    Article Snippet: Platinum-based antitumor drugs, such as cisplatin and carboplatin, are well-known for their severe ototoxicity.. The ototoxic effects of these drugs are primarily attributed to oxidative stress induced damage within cochlear hair cells (HCs), leading to cell death and subsequent irreversible hearing loss.. Over the past decade, studies have demonstrated that upregulating autophagy levels in HCs can greatly alleviate the death of cochlear HCs as part of the oxidative damage induced by ototoxic drugs.



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    APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and <t>Beclin1</t> proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).
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    APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and <t>Beclin1</t> proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).
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    APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and <t>Beclin1</t> proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).
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    APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and <t>Beclin1</t> proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).
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    APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and <t>Beclin1</t> proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).
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    APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and <t>Beclin1</t> proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).
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    APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and <t>Beclin1</t> proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).
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    APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and <t>Beclin1</t> proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).
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    APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and <t>Beclin1</t> proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).
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    Image Search Results


    APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and Beclin1 proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).

    Journal: Veterinary Research

    Article Title: Outer membrane vesicles secreted by avian pathogenic Escherichia coli promote its survival within macrophages and systemic infection by inducing endoplasmic reticulum stress-mediated autophagy flux blockade

    doi: 10.1186/s13567-025-01679-6

    Figure Lengend Snippet: APEC OMVs induce incomplete autophagy in HD11 cells . A HD11 cells were treated with OMVs (100 µg/mL) for 6 h, and typical double-membrane autophagosomes were observed by transmission electron microscopy. Scale bar,500 nm. B , C HD11 cells were treated with OMVs (100 µg/mL) for 0–9 h, western blot analysis was performed to detect the expression of LC3-II, p62, and Beclin1 proteins in cell lysates, and gray value analysis was performed using ImageJ software ( C ) ( n = 3). D Immunofluorescence was used to detect the effect of OMVs (100 µg/mL) on the colocalization of LC3 and the lysosomal marker protein LAMP1 in HD11 cells. The data are representative of three independent experiments. Scale bar, 5 μm. Colocalization scatter plots were generated using ImageJ software and GraphPad Prism 8. n represents three biological replicates, with each data point corresponding to an independent culture system. Bar charts display mean ± standard error of the mean (SEM), analyzed by Student’s -test (* p < 0.05, ** p < 0.01, *** p < 0.001).

    Article Snippet: Rabbit anti-Beclin1 polyclonal antibody , Bioss, Beijing, China , 1:2000.

    Techniques: Membrane, Transmission Assay, Electron Microscopy, Western Blot, Expressing, Software, Immunofluorescence, Marker, Generated