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arrayit huprot™ v2.0 19 k human proteome microarrays  (CDI Laboratories)

 
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    CDI Laboratories arrayit huprot™ v2.0 19 k human proteome microarrays
    Arrayit Huprot™ V2.0 19 K Human Proteome Microarrays, supplied by CDI Laboratories, 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/product/huprot+human+proteome+microarray+v2%2E0/huprot+human+proteome+microarray/pm39884078-86-5-8
    Average 90 stars, based on 1 article reviews
    arrayit huprot™ v2.0 19 k human proteome microarrays - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Microarray:

    Article Title: Drp1-Zip1 Interaction Regulates Mitochondrial Quality Surveillance System.
    Article Snippet: The HuProt human proteome microarray v2.0 (CDI Laboratories) was used for the detection of Drp1-interacting proteins, and the experiment was performed according to the manufacturer’s protocol, with some modifications: Each protein chip was equilibrated with microarray buffer containing (137 mM NaCl, 2.7 mM KCl, 4.3 mM Na2HPO4, 1.47 mM KH2PO4, pH 7.4, 0.1% Triton X-100) for 5 min at RT and sequentially incubated with blocking solution composed of 5% IgG-free BSA (Jackson ImmunoResearch) in microarray buffer for 30 min at RT.

    Article Title: PELI1 Selectively Targets Kinase-Active RIP3 for Ubiquitylation-Dependent Proteasomal Degradation.
    Article Snippet: The protein microarray experiment was performed by using a HuProt human proteome microarray v2.0 (CDI Laboratories).

    Incubation:

    Article Title: Drp1-Zip1 Interaction Regulates Mitochondrial Quality Surveillance System.
    Article Snippet: The HuProt human proteome microarray v2.0 (CDI Laboratories) was used for the detection of Drp1-interacting proteins, and the experiment was performed according to the manufacturer’s protocol, with some modifications: Each protein chip was equilibrated with microarray buffer containing (137 mM NaCl, 2.7 mM KCl, 4.3 mM Na2HPO4, 1.47 mM KH2PO4, pH 7.4, 0.1% Triton X-100) for 5 min at RT and sequentially incubated with blocking solution composed of 5% IgG-free BSA (Jackson ImmunoResearch) in microarray buffer for 30 min at RT.

    Article Title: PELI1 Selectively Targets Kinase-Active RIP3 for Ubiquitylation-Dependent Proteasomal Degradation.
    Article Snippet: The protein microarray experiment was performed by using a HuProt human proteome microarray v2.0 (CDI Laboratories).

    Blocking Assay:

    Article Title: Drp1-Zip1 Interaction Regulates Mitochondrial Quality Surveillance System.
    Article Snippet: The HuProt human proteome microarray v2.0 (CDI Laboratories) was used for the detection of Drp1-interacting proteins, and the experiment was performed according to the manufacturer’s protocol, with some modifications: Each protein chip was equilibrated with microarray buffer containing (137 mM NaCl, 2.7 mM KCl, 4.3 mM Na2HPO4, 1.47 mM KH2PO4, pH 7.4, 0.1% Triton X-100) for 5 min at RT and sequentially incubated with blocking solution composed of 5% IgG-free BSA (Jackson ImmunoResearch) in microarray buffer for 30 min at RT.

    Article Title: PELI1 Selectively Targets Kinase-Active RIP3 for Ubiquitylation-Dependent Proteasomal Degradation.
    Article Snippet: The protein microarray experiment was performed by using a HuProt human proteome microarray v2.0 (CDI Laboratories).



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    arrayit huprot™ v2.0 19 k human proteome microarrays  (CDI Laboratories)
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    CDI Laboratories arrayit huprot™ v2.0 19 k human proteome microarrays
    Arrayit Huprot™ V2.0 19 K Human Proteome Microarrays, supplied by CDI Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    arrayit huprot v2.0 19k human proteome microarray  (CDI Laboratories)
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    A Human <t>proteome</t> microarray showing potential interacting proteins with Biotin-tagged Drp1 protein. Red arrow indicated the positive control (Biotin-BSA), yellow arrow indicated the negative control (BSA protein), and white arrow indicated LRRK2, our interested potential interacting proteins with Biotin-tagged Drp1 protein. B Co-IP results for the combination of Drp1 and LRRK2 in total, cytoplasmic and mitochondrial fractions of VSMCs after hypoxia. ( n = 3 samples/group). C Representative immunofluorescence images showing the co-location of Drp1 (red), LRRK2 (green) and mitochondria (white) in VSMCs after hypoxia. (bar, 5 μm). D Molecular docking of Drp1 to LRRK2 in hypoxia conditions determined by GRAMM-X Protein-Protein Docking program. The blue dotted indicated the stable hydrogen bond between Drp1 Thr595 and LRRK2 Gly2019. E Co-IP results for the combination of Drp1 and LRRK2 in hypoxia-induced VSMCs after Drp1 T595A mutation. F The phosphorylation of HK2-Thr 473 and HK2 expression in total, cytoplasmic and mitochondrial fractions of hypoxia-induced VSMCs after Drp1 T595A mutation. β-actin, Tubulin and COX IV were used as interior references of total, cytoplasmic and mitochondrial fractions. G Representative confocal images of mPTP opening in hypoxia-induced VSMCs after Drp1 T595A mutation. (bar, 100 μm). a: P < 0.05 compared with Normal group.
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    huprot human proteome microarray v2.0  (CDI Laboratories)
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    A Human <t>proteome</t> microarray showing potential interacting proteins with Biotin-tagged Drp1 protein. Red arrow indicated the positive control (Biotin-BSA), yellow arrow indicated the negative control (BSA protein), and white arrow indicated LRRK2, our interested potential interacting proteins with Biotin-tagged Drp1 protein. B Co-IP results for the combination of Drp1 and LRRK2 in total, cytoplasmic and mitochondrial fractions of VSMCs after hypoxia. ( n = 3 samples/group). C Representative immunofluorescence images showing the co-location of Drp1 (red), LRRK2 (green) and mitochondria (white) in VSMCs after hypoxia. (bar, 5 μm). D Molecular docking of Drp1 to LRRK2 in hypoxia conditions determined by GRAMM-X Protein-Protein Docking program. The blue dotted indicated the stable hydrogen bond between Drp1 Thr595 and LRRK2 Gly2019. E Co-IP results for the combination of Drp1 and LRRK2 in hypoxia-induced VSMCs after Drp1 T595A mutation. F The phosphorylation of HK2-Thr 473 and HK2 expression in total, cytoplasmic and mitochondrial fractions of hypoxia-induced VSMCs after Drp1 T595A mutation. β-actin, Tubulin and COX IV were used as interior references of total, cytoplasmic and mitochondrial fractions. G Representative confocal images of mPTP opening in hypoxia-induced VSMCs after Drp1 T595A mutation. (bar, 100 μm). a: P < 0.05 compared with Normal group.
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    protein microarray a huprot (tm) human proteome microarray v2.0  (Filgen Inc)
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    A Human <t>proteome</t> microarray showing potential interacting proteins with Biotin-tagged Drp1 protein. Red arrow indicated the positive control (Biotin-BSA), yellow arrow indicated the negative control (BSA protein), and white arrow indicated LRRK2, our interested potential interacting proteins with Biotin-tagged Drp1 protein. B Co-IP results for the combination of Drp1 and LRRK2 in total, cytoplasmic and mitochondrial fractions of VSMCs after hypoxia. ( n = 3 samples/group). C Representative immunofluorescence images showing the co-location of Drp1 (red), LRRK2 (green) and mitochondria (white) in VSMCs after hypoxia. (bar, 5 μm). D Molecular docking of Drp1 to LRRK2 in hypoxia conditions determined by GRAMM-X Protein-Protein Docking program. The blue dotted indicated the stable hydrogen bond between Drp1 Thr595 and LRRK2 Gly2019. E Co-IP results for the combination of Drp1 and LRRK2 in hypoxia-induced VSMCs after Drp1 T595A mutation. F The phosphorylation of HK2-Thr 473 and HK2 expression in total, cytoplasmic and mitochondrial fractions of hypoxia-induced VSMCs after Drp1 T595A mutation. β-actin, Tubulin and COX IV were used as interior references of total, cytoplasmic and mitochondrial fractions. G Representative confocal images of mPTP opening in hypoxia-induced VSMCs after Drp1 T595A mutation. (bar, 100 μm). a: P < 0.05 compared with Normal group.
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    A Human <t>proteome</t> microarray showing potential interacting proteins with Biotin-tagged Drp1 protein. Red arrow indicated the positive control (Biotin-BSA), yellow arrow indicated the negative control (BSA protein), and white arrow indicated LRRK2, our interested potential interacting proteins with Biotin-tagged Drp1 protein. B Co-IP results for the combination of Drp1 and LRRK2 in total, cytoplasmic and mitochondrial fractions of VSMCs after hypoxia. ( n = 3 samples/group). C Representative immunofluorescence images showing the co-location of Drp1 (red), LRRK2 (green) and mitochondria (white) in VSMCs after hypoxia. (bar, 5 μm). D Molecular docking of Drp1 to LRRK2 in hypoxia conditions determined by GRAMM-X Protein-Protein Docking program. The blue dotted indicated the stable hydrogen bond between Drp1 Thr595 and LRRK2 Gly2019. E Co-IP results for the combination of Drp1 and LRRK2 in hypoxia-induced VSMCs after Drp1 T595A mutation. F The phosphorylation of HK2-Thr 473 and HK2 expression in total, cytoplasmic and mitochondrial fractions of hypoxia-induced VSMCs after Drp1 T595A mutation. β-actin, Tubulin and COX IV were used as interior references of total, cytoplasmic and mitochondrial fractions. G Representative confocal images of mPTP opening in hypoxia-induced VSMCs after Drp1 T595A mutation. (bar, 100 μm). a: P < 0.05 compared with Normal group.
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    Image Search Results


    A Human proteome microarray showing potential interacting proteins with Biotin-tagged Drp1 protein. Red arrow indicated the positive control (Biotin-BSA), yellow arrow indicated the negative control (BSA protein), and white arrow indicated LRRK2, our interested potential interacting proteins with Biotin-tagged Drp1 protein. B Co-IP results for the combination of Drp1 and LRRK2 in total, cytoplasmic and mitochondrial fractions of VSMCs after hypoxia. ( n = 3 samples/group). C Representative immunofluorescence images showing the co-location of Drp1 (red), LRRK2 (green) and mitochondria (white) in VSMCs after hypoxia. (bar, 5 μm). D Molecular docking of Drp1 to LRRK2 in hypoxia conditions determined by GRAMM-X Protein-Protein Docking program. The blue dotted indicated the stable hydrogen bond between Drp1 Thr595 and LRRK2 Gly2019. E Co-IP results for the combination of Drp1 and LRRK2 in hypoxia-induced VSMCs after Drp1 T595A mutation. F The phosphorylation of HK2-Thr 473 and HK2 expression in total, cytoplasmic and mitochondrial fractions of hypoxia-induced VSMCs after Drp1 T595A mutation. β-actin, Tubulin and COX IV were used as interior references of total, cytoplasmic and mitochondrial fractions. G Representative confocal images of mPTP opening in hypoxia-induced VSMCs after Drp1 T595A mutation. (bar, 100 μm). a: P < 0.05 compared with Normal group.

    Journal: Cell Death & Disease

    Article Title: Mitochondrial Drp1 recognizes and induces excessive mPTP opening after hypoxia through BAX-PiC and LRRK2-HK2

    doi: 10.1038/s41419-021-04343-x

    Figure Lengend Snippet: A Human proteome microarray showing potential interacting proteins with Biotin-tagged Drp1 protein. Red arrow indicated the positive control (Biotin-BSA), yellow arrow indicated the negative control (BSA protein), and white arrow indicated LRRK2, our interested potential interacting proteins with Biotin-tagged Drp1 protein. B Co-IP results for the combination of Drp1 and LRRK2 in total, cytoplasmic and mitochondrial fractions of VSMCs after hypoxia. ( n = 3 samples/group). C Representative immunofluorescence images showing the co-location of Drp1 (red), LRRK2 (green) and mitochondria (white) in VSMCs after hypoxia. (bar, 5 μm). D Molecular docking of Drp1 to LRRK2 in hypoxia conditions determined by GRAMM-X Protein-Protein Docking program. The blue dotted indicated the stable hydrogen bond between Drp1 Thr595 and LRRK2 Gly2019. E Co-IP results for the combination of Drp1 and LRRK2 in hypoxia-induced VSMCs after Drp1 T595A mutation. F The phosphorylation of HK2-Thr 473 and HK2 expression in total, cytoplasmic and mitochondrial fractions of hypoxia-induced VSMCs after Drp1 T595A mutation. β-actin, Tubulin and COX IV were used as interior references of total, cytoplasmic and mitochondrial fractions. G Representative confocal images of mPTP opening in hypoxia-induced VSMCs after Drp1 T595A mutation. (bar, 100 μm). a: P < 0.05 compared with Normal group.

    Article Snippet: Arrayit HuProt™ v2.0 19K Human Proteome Microarrays (CDI Laboratories, Baltimore, MD, USA) were used to identify Drp1-interacting proteins.

    Techniques: Microarray, Positive Control, Negative Control, Co-Immunoprecipitation Assay, Immunofluorescence, Mutagenesis, Expressing