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capturemtm ip co ip kit  (TaKaRa)


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    TaKaRa capturemtm ip co ip kit
    Capturemtm Ip Co Ip Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 95/100, based on 80 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/capturemtm ip co ip kit/product/TaKaRa
    Average 95 stars, based on 80 article reviews
    capturemtm ip co ip kit - by Bioz Stars, 2026-02
    95/100 stars

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    Inflammatory cytokines and viruses were detected in the <t>extracellular</t> vesicles of CV-A10-infected cells. ( A ) A heatmap presenting the results of inflammatory cytokines in extracellular vesicles by flow cytometry. ( B ) The proliferative dynamics of CV-A10 in extracellular vesicles were assessed by monitoring the viral load, virus titer, and VP1 expression via qRT-PCR, TCID 50 , and WB assays, respectively.
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    Inflammatory cytokines and viruses were detected in the <t>extracellular</t> vesicles of CV-A10-infected cells. ( A ) A heatmap presenting the results of inflammatory cytokines in extracellular vesicles by flow cytometry. ( B ) The proliferative dynamics of CV-A10 in extracellular vesicles were assessed by monitoring the viral load, virus titer, and VP1 expression via qRT-PCR, TCID 50 , and WB assays, respectively.
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    Inflammatory cytokines and viruses were detected in the extracellular vesicles of CV-A10-infected cells. ( A ) A heatmap presenting the results of inflammatory cytokines in extracellular vesicles by flow cytometry. ( B ) The proliferative dynamics of CV-A10 in extracellular vesicles were assessed by monitoring the viral load, virus titer, and VP1 expression via qRT-PCR, TCID 50 , and WB assays, respectively.

    Journal: Microbiology Spectrum

    Article Title: Coxsackievirus A10 blocks autophagosome-lysosome fusion to promote viral nonlytic spread and inflammatory cytokine release

    doi: 10.1128/spectrum.00830-25

    Figure Lengend Snippet: Inflammatory cytokines and viruses were detected in the extracellular vesicles of CV-A10-infected cells. ( A ) A heatmap presenting the results of inflammatory cytokines in extracellular vesicles by flow cytometry. ( B ) The proliferative dynamics of CV-A10 in extracellular vesicles were assessed by monitoring the viral load, virus titer, and VP1 expression via qRT-PCR, TCID 50 , and WB assays, respectively.

    Article Snippet: In this study, we used the commercial Capture Extracellular Vesicle Isolation Kit (Takara, Japan), following the manufacturer’s instructions to obtain extracellular vesicles.

    Techniques: Infection, Flow Cytometry, Virus, Expressing, Quantitative RT-PCR

    The autophagic secretory pathway was involved in the release of inflammatory cytokines and viruses during CV-A10 infection. ( A ) Protein expression levels of the autophagic secretory pathway were measured by WB in CV-A10-infected HUVECs subjected to different treatments. ( B ) A heatmap presenting the results of inflammatory cytokines in extracellular vesicles through flow cytometry in CV-A10-infected HUVECs subjected to different treatments. ( C ) Examination of extracellular viral RNA, virus titer, and VP1 protein from CV-A10-infected HUVECs subjected to different treatments by qRT-PCR, TCID 50 , and WB assays, respectively.

    Journal: Microbiology Spectrum

    Article Title: Coxsackievirus A10 blocks autophagosome-lysosome fusion to promote viral nonlytic spread and inflammatory cytokine release

    doi: 10.1128/spectrum.00830-25

    Figure Lengend Snippet: The autophagic secretory pathway was involved in the release of inflammatory cytokines and viruses during CV-A10 infection. ( A ) Protein expression levels of the autophagic secretory pathway were measured by WB in CV-A10-infected HUVECs subjected to different treatments. ( B ) A heatmap presenting the results of inflammatory cytokines in extracellular vesicles through flow cytometry in CV-A10-infected HUVECs subjected to different treatments. ( C ) Examination of extracellular viral RNA, virus titer, and VP1 protein from CV-A10-infected HUVECs subjected to different treatments by qRT-PCR, TCID 50 , and WB assays, respectively.

    Article Snippet: In this study, we used the commercial Capture Extracellular Vesicle Isolation Kit (Takara, Japan), following the manufacturer’s instructions to obtain extracellular vesicles.

    Techniques: Infection, Expressing, Flow Cytometry, Virus, Quantitative RT-PCR