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v v optiprep  (New England Biolabs)


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    New England Biolabs v v optiprep
    V V Optiprep, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 100 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/v v optiprep/product/New England Biolabs
    Average 96 stars, based on 100 article reviews
    v v optiprep - by Bioz Stars, 2026-03
    96/100 stars

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    Bodipy sEV separate as a single peak enriched in tetraspanins . (a) Bodipy sEV 100K pellets were loaded at the bottom of an <t>iodixanol</t> density gradient and ultracentrifuged for 16 h. Fractions were collected from the top of the gradient and were analyzed for Bodipy sEV number by FC before and after the addition of Octyl‐beta‐glucoside (OG). Data are expressed as mean ± SEM ( n = 14). (b) 100K pellets from conditioned media of untreated Mel501 cells were incubated with CFSE to non specifically label the total population of sEV and loaded at the bottom of an iodixanol density gradient. Data are expressed as mean ± SEM ( n = 4). (c) Density of the fractions was measured by refractometry. Data are expressed as mean ± SEM ( n = 17). (d) The total volume of each fraction was analyzed by Western blot. Data shown are representative of three independent experiments. (d) Analysis of colocalization of tetraspanins fluorescent antibodies with Bodipy sEV.
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    Bodipy sEV separate as a single peak enriched in tetraspanins . (a) Bodipy sEV 100K pellets were loaded at the bottom of an iodixanol density gradient and ultracentrifuged for 16 h. Fractions were collected from the top of the gradient and were analyzed for Bodipy sEV number by FC before and after the addition of Octyl‐beta‐glucoside (OG). Data are expressed as mean ± SEM ( n = 14). (b) 100K pellets from conditioned media of untreated Mel501 cells were incubated with CFSE to non specifically label the total population of sEV and loaded at the bottom of an iodixanol density gradient. Data are expressed as mean ± SEM ( n = 4). (c) Density of the fractions was measured by refractometry. Data are expressed as mean ± SEM ( n = 17). (d) The total volume of each fraction was analyzed by Western blot. Data shown are representative of three independent experiments. (d) Analysis of colocalization of tetraspanins fluorescent antibodies with Bodipy sEV.

    Journal: Journal of Extracellular Vesicles

    Article Title: Metabolic labelling of a subpopulation of small extracellular vesicles using a fluorescent palmitic acid analogue

    doi: 10.1002/jev2.12392

    Figure Lengend Snippet: Bodipy sEV separate as a single peak enriched in tetraspanins . (a) Bodipy sEV 100K pellets were loaded at the bottom of an iodixanol density gradient and ultracentrifuged for 16 h. Fractions were collected from the top of the gradient and were analyzed for Bodipy sEV number by FC before and after the addition of Octyl‐beta‐glucoside (OG). Data are expressed as mean ± SEM ( n = 14). (b) 100K pellets from conditioned media of untreated Mel501 cells were incubated with CFSE to non specifically label the total population of sEV and loaded at the bottom of an iodixanol density gradient. Data are expressed as mean ± SEM ( n = 4). (c) Density of the fractions was measured by refractometry. Data are expressed as mean ± SEM ( n = 17). (d) The total volume of each fraction was analyzed by Western blot. Data shown are representative of three independent experiments. (d) Analysis of colocalization of tetraspanins fluorescent antibodies with Bodipy sEV.

    Article Snippet: Bodipy sEV (100K pellets) were bottom loaded in a discontinuous iodixanol gradient (35% (w/v), 25% (w/v), 15% (w/v) and 5% (w/v)) made by diluting OptiPrep (60% (w/v)) iodixanol (Sigma‐Aldrich, #D1556) with 60 mM Tris‐HCl (pH7.4), 0.25 M sucrose, 1 mM of EDTA from the bottom to the top of an open‐top polypropylene tube (Beckman Coulter, #328874).

    Techniques: Incubation, Western Blot