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rabbit polyclonal  (Proteintech)


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    Structured Review

    Proteintech rabbit polyclonal
    Rabbit Polyclonal, 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/rabbit+beclin+1+polyclonal+antibody/Beclin+1+Antibody/pm41138645-42-3-47
    Average 96 stars, based on 1517 article reviews
    rabbit polyclonal - by Bioz Stars, 2026-10
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    Marker:

    Article Title: Bone marrow mesenchymal stem cells repair spinal cord ischemia/reperfusion injury by promoting axonal growth and anti-autophagy
    Article Snippet: .. Rabbit anti-growth associated protein-43 polyclonal antibody (1:1,000), rabbit anti-neurofilament-H (marker for mature neuronal axons) (Yabe et al., 2001) polyclonal antibody (1:1,000; Proteintech Group), rabbit anti-rat light chain 3B monoclonal antibody (1:1,000), or rabbit-Beclin 1 polyclonal antibody (1:1,000) were added overnight at 4°C. .. Mouse anti-rat β-actin monoclonal antibody (1:2,000; Proteintech Group) served as the reference marker/positive control.



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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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    Proteintech beclin 1 rabbit polyclonal antibody
    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