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primary antibodies parkin  (ZenBio)

 
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    Structured Review

    ZenBio primary antibodies parkin
    Aloe‐emodin activates mitophagy in ad mice neurons. (A) Fluorescence staining of Parkin (red) in the mouse hippocampus. The cell nuclei were stained with DAPI (blue). (B) Double fluorescence staining of <t>LC3B</t> (red) and Neun (green) in the mouse hippocampus. (C) Double fluorescence staining of p‐AMPK (green) and SIRT3 (red) among mouse hippocampus. Scale bar = 20 μm. (D) Statistical analysis of the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 in comparison with the WT group, * p < 0.05 in comparison with the ad group.
    Primary Antibodies Parkin, supplied by ZenBio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies parkin/product/ZenBio
    Average 90 stars, based on 1 article reviews
    primary antibodies parkin - by Bioz Stars, 2026-06
    90/100 stars

    Images

    1) Product Images from "Aloe‐Emodin Improves Mitophagy in Alzheimer's Disease via Activating the AMPK / PGC ‐1α/ SIRT3 Signaling Pathway"

    Article Title: Aloe‐Emodin Improves Mitophagy in Alzheimer's Disease via Activating the AMPK / PGC ‐1α/ SIRT3 Signaling Pathway

    Journal: CNS Neuroscience & Therapeutics

    doi: 10.1111/cns.70346

    Aloe‐emodin activates mitophagy in ad mice neurons. (A) Fluorescence staining of Parkin (red) in the mouse hippocampus. The cell nuclei were stained with DAPI (blue). (B) Double fluorescence staining of LC3B (red) and Neun (green) in the mouse hippocampus. (C) Double fluorescence staining of p‐AMPK (green) and SIRT3 (red) among mouse hippocampus. Scale bar = 20 μm. (D) Statistical analysis of the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 in comparison with the WT group, * p < 0.05 in comparison with the ad group.
    Figure Legend Snippet: Aloe‐emodin activates mitophagy in ad mice neurons. (A) Fluorescence staining of Parkin (red) in the mouse hippocampus. The cell nuclei were stained with DAPI (blue). (B) Double fluorescence staining of LC3B (red) and Neun (green) in the mouse hippocampus. (C) Double fluorescence staining of p‐AMPK (green) and SIRT3 (red) among mouse hippocampus. Scale bar = 20 μm. (D) Statistical analysis of the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 in comparison with the WT group, * p < 0.05 in comparison with the ad group.

    Techniques Used: Fluorescence, Staining, Comparison

    AE treatment modulates mitophagy and proteins related to the AMPK/PGC‐1α/SIRT3 pathway. (A) Western blot results of AMPK, p‐AMPK, PGC‐1α, SIRT3, and mitophagy‐related proteins (LC3B, P62, Beclin1) in HT22 cells. (B) Statistical analysis of the western blotting results. (C) Fluorescence staining of p‐AMPK, AMPK (red), and DAPI (blue) among HT22 cells. (D) Fluorescence staining of LC3B (green) and DAPI (blue) among the ditto cells. (E) Fluorescence staining of P62 (red) and DAPI (blue) among the ditto cells. Scale bar = 20 μm. (F) Statistical analysis on the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 by contrast with the WT group, * p < 0.05 by contrast with the ad group.
    Figure Legend Snippet: AE treatment modulates mitophagy and proteins related to the AMPK/PGC‐1α/SIRT3 pathway. (A) Western blot results of AMPK, p‐AMPK, PGC‐1α, SIRT3, and mitophagy‐related proteins (LC3B, P62, Beclin1) in HT22 cells. (B) Statistical analysis of the western blotting results. (C) Fluorescence staining of p‐AMPK, AMPK (red), and DAPI (blue) among HT22 cells. (D) Fluorescence staining of LC3B (green) and DAPI (blue) among the ditto cells. (E) Fluorescence staining of P62 (red) and DAPI (blue) among the ditto cells. Scale bar = 20 μm. (F) Statistical analysis on the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 by contrast with the WT group, * p < 0.05 by contrast with the ad group.

    Techniques Used: Western Blot, Fluorescence, Staining



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    ZenBio primary antibodies parkin
    Aloe‐emodin activates mitophagy in ad mice neurons. (A) Fluorescence staining of Parkin (red) in the mouse hippocampus. The cell nuclei were stained with DAPI (blue). (B) Double fluorescence staining of <t>LC3B</t> (red) and Neun (green) in the mouse hippocampus. (C) Double fluorescence staining of p‐AMPK (green) and SIRT3 (red) among mouse hippocampus. Scale bar = 20 μm. (D) Statistical analysis of the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 in comparison with the WT group, * p < 0.05 in comparison with the ad group.
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    primary antibodies pink1, parkin, p62, and lc3  (Servicebio Inc)
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    Aloe‐emodin activates mitophagy in ad mice neurons. (A) Fluorescence staining of Parkin (red) in the mouse hippocampus. The cell nuclei were stained with DAPI (blue). (B) Double fluorescence staining of <t>LC3B</t> (red) and Neun (green) in the mouse hippocampus. (C) Double fluorescence staining of p‐AMPK (green) and SIRT3 (red) among mouse hippocampus. Scale bar = 20 μm. (D) Statistical analysis of the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 in comparison with the WT group, * p < 0.05 in comparison with the ad group.
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    Image Search Results


    Aloe‐emodin activates mitophagy in ad mice neurons. (A) Fluorescence staining of Parkin (red) in the mouse hippocampus. The cell nuclei were stained with DAPI (blue). (B) Double fluorescence staining of LC3B (red) and Neun (green) in the mouse hippocampus. (C) Double fluorescence staining of p‐AMPK (green) and SIRT3 (red) among mouse hippocampus. Scale bar = 20 μm. (D) Statistical analysis of the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 in comparison with the WT group, * p < 0.05 in comparison with the ad group.

    Journal: CNS Neuroscience & Therapeutics

    Article Title: Aloe‐Emodin Improves Mitophagy in Alzheimer's Disease via Activating the AMPK / PGC ‐1α/ SIRT3 Signaling Pathway

    doi: 10.1111/cns.70346

    Figure Lengend Snippet: Aloe‐emodin activates mitophagy in ad mice neurons. (A) Fluorescence staining of Parkin (red) in the mouse hippocampus. The cell nuclei were stained with DAPI (blue). (B) Double fluorescence staining of LC3B (red) and Neun (green) in the mouse hippocampus. (C) Double fluorescence staining of p‐AMPK (green) and SIRT3 (red) among mouse hippocampus. Scale bar = 20 μm. (D) Statistical analysis of the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 in comparison with the WT group, * p < 0.05 in comparison with the ad group.

    Article Snippet: Diluted primary antibodies LC3B (Zenbio), Parkin (Zenbio), SIRT3 (Affinity), and p‐AMPK (Beyotime) were added and nurtured at 4°C.

    Techniques: Fluorescence, Staining, Comparison

    AE treatment modulates mitophagy and proteins related to the AMPK/PGC‐1α/SIRT3 pathway. (A) Western blot results of AMPK, p‐AMPK, PGC‐1α, SIRT3, and mitophagy‐related proteins (LC3B, P62, Beclin1) in HT22 cells. (B) Statistical analysis of the western blotting results. (C) Fluorescence staining of p‐AMPK, AMPK (red), and DAPI (blue) among HT22 cells. (D) Fluorescence staining of LC3B (green) and DAPI (blue) among the ditto cells. (E) Fluorescence staining of P62 (red) and DAPI (blue) among the ditto cells. Scale bar = 20 μm. (F) Statistical analysis on the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 by contrast with the WT group, * p < 0.05 by contrast with the ad group.

    Journal: CNS Neuroscience & Therapeutics

    Article Title: Aloe‐Emodin Improves Mitophagy in Alzheimer's Disease via Activating the AMPK / PGC ‐1α/ SIRT3 Signaling Pathway

    doi: 10.1111/cns.70346

    Figure Lengend Snippet: AE treatment modulates mitophagy and proteins related to the AMPK/PGC‐1α/SIRT3 pathway. (A) Western blot results of AMPK, p‐AMPK, PGC‐1α, SIRT3, and mitophagy‐related proteins (LC3B, P62, Beclin1) in HT22 cells. (B) Statistical analysis of the western blotting results. (C) Fluorescence staining of p‐AMPK, AMPK (red), and DAPI (blue) among HT22 cells. (D) Fluorescence staining of LC3B (green) and DAPI (blue) among the ditto cells. (E) Fluorescence staining of P62 (red) and DAPI (blue) among the ditto cells. Scale bar = 20 μm. (F) Statistical analysis on the IF results. The outcomes were denoted as mean ± SEM( n = 3). # p < 0.05 by contrast with the WT group, * p < 0.05 by contrast with the ad group.

    Article Snippet: Diluted primary antibodies LC3B (Zenbio), Parkin (Zenbio), SIRT3 (Affinity), and p‐AMPK (Beyotime) were added and nurtured at 4°C.

    Techniques: Western Blot, Fluorescence, Staining