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405 430 mb405 biotium  (Biotium)


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    Biotium 405 430 mb405 biotium
    405 430 Mb405 Biotium, supplied by Biotium, used in various techniques. Bioz Stars score: 93/100, based on 23 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/membrite+fix+cell+surface+staining+kits/MemBrite+Fix+405%2F430+Cell+Surface+Staining+Kit/pm41349547-828-78-80
    Average 93 stars, based on 23 article reviews
    405 430 mb405 biotium - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Staining:

    Article Title: HERV-K (HML-2) Envelope Protein Induces Mitochondrial Depolarization and Neurotoxicity via Endolysosome Iron Dyshomeostasis
    Article Snippet: Peter W. Halcrow, Darius N.K.. Quansah,* Nirmal Kumar,* Joseph P. Steiner, Avindra Nath, and Jonathan D. Geiger Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota 58202 and Section for Infections of the Nervous System, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892

    Article Title: Epstein-Barr virus BALF0/1 subverts the Caveolin and ERAD pathways to target B cell receptor complexes for degradation.
    Article Snippet: Image acquisition and analysis was performed with a Zeiss LSM 800 instrument and with Zeiss Zen Lite (Blue) software, respectively. .. PM staining was performed using MemBrite Fix Cell Surface Staining Kits (Catalog#: 30098-T, Biotium), according to the manufacturer’s protocol. ..

    Microscopy:

    Article Title: HERV-K (HML-2) Envelope Protein Induces Mitochondrial Depolarization and Neurotoxicity via Endolysosome Iron Dyshomeostasis
    Article Snippet: Peter W. Halcrow, Darius N.K.. Quansah,* Nirmal Kumar,* Joseph P. Steiner, Avindra Nath, and Jonathan D. Geiger Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota 58202 and Section for Infections of the Nervous System, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892



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    (A) Immunofluorescence microscopy displaying localization of PLD4 (red) at TGN46-tagged trans Golgi networks (green) in resting B cells and translocation of PLD4 from trans Golgi networks in CpG/anti-IgG + M stimulated B cells, compared to the control cells. (B) Immunofluorescence microscopy shows enhanced expression of PLD4 (red) and co-localization of PLD4 and CD63 (green) in CpG/anti-IgG + M stimulated B cells, compared to the control cells. Cell membranes stained with <t>MemBrite</t> appeared thicker in CpG/anti-IgG + M stimulated B cells than in the control cells. (C) Statistical analysis revealing enhanced PLD4 expression in each CpG/anti-IgG + M stimulated B cell compared to the control cells. Bar; 10 μm, **P < 0.01, ***P < 0.001.
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    Image Search Results


    (A) Immunofluorescence microscopy displaying localization of PLD4 (red) at TGN46-tagged trans Golgi networks (green) in resting B cells and translocation of PLD4 from trans Golgi networks in CpG/anti-IgG + M stimulated B cells, compared to the control cells. (B) Immunofluorescence microscopy shows enhanced expression of PLD4 (red) and co-localization of PLD4 and CD63 (green) in CpG/anti-IgG + M stimulated B cells, compared to the control cells. Cell membranes stained with MemBrite appeared thicker in CpG/anti-IgG + M stimulated B cells than in the control cells. (C) Statistical analysis revealing enhanced PLD4 expression in each CpG/anti-IgG + M stimulated B cell compared to the control cells. Bar; 10 μm, **P < 0.01, ***P < 0.001.

    Journal: PLOS One

    Article Title: Activated human B cells produce phospholipase D4-containing extracellular vesicles

    doi: 10.1371/journal.pone.0329832

    Figure Lengend Snippet: (A) Immunofluorescence microscopy displaying localization of PLD4 (red) at TGN46-tagged trans Golgi networks (green) in resting B cells and translocation of PLD4 from trans Golgi networks in CpG/anti-IgG + M stimulated B cells, compared to the control cells. (B) Immunofluorescence microscopy shows enhanced expression of PLD4 (red) and co-localization of PLD4 and CD63 (green) in CpG/anti-IgG + M stimulated B cells, compared to the control cells. Cell membranes stained with MemBrite appeared thicker in CpG/anti-IgG + M stimulated B cells than in the control cells. (C) Statistical analysis revealing enhanced PLD4 expression in each CpG/anti-IgG + M stimulated B cell compared to the control cells. Bar; 10 μm, **P < 0.01, ***P < 0.001.

    Article Snippet: Plasma membranes were stained using the MemBrite ® Fix Cell Surface Staining Kits – MemBrite ® Fix 680/700 (SKU: 30099-T; Biotium, Fremont, CA, USA).

    Techniques: Immunofluorescence, Microscopy, Translocation Assay, Control, Expressing, Staining