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mouse anti o4 igm  (Novus Biologicals)


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    Novus Biologicals mouse anti o4 igm
    Mouse Anti O4 Igm, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+o4+igm/Mouse+anti-Rabbit+IgM+(H%2BL)+Secondary+Antibody+(NRBM)/ppr0957196-78-4-8
    Average 93 stars, based on 5 article reviews
    mouse anti o4 igm - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    Marker:

    Article Title: Patient-Specific and Regional Factors Influencing Proliferation Dynamics of Adult Human Neural Stem/Progenitor Cells from Spinal Cord Tissue
    Article Snippet: .. The antibodies used included: mouse anti-O4 IgM (1:500) (Novus Biologicals, MAB1326) for oligodendrocytes, mouse anti-β-III tubulin IgG (1:500) (STEMCELL Technologies, 01409) (SantaCruz, 80005) for immature neurons, rabbit anti-GFAP IgG (1:1000) (EMD Millipore, Ab5804) for astrocytes, mouse anti-Nestin (10C2) IgG (1:500) (SantaCruz, 23927) to label human progenitor cells, rabbit anti-Sox2 IgG (1:1000) (Abcam, ab97959) for neural stem cells, and mouse anti-BrdU IgG (1:2000) (EMD Millipore, MAB4072) as a proliferation marker. ..



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    Expression of oligodendrocyte marker <t>O4</t> by OPCs incubated with H. elongata and S. fusiforme lipid extracts. The surface area percentage of O4 staining, as a marker of pre-oligodendrocytes, was determined on cultured OPCs incubated with lipid extracts of H. elongata and S. fusiforme . The extracts were added based on saringosterol concentration, with a final saringosterol concentration of 0.6 µM. The O4 expression was normalized to the surface area percentage of a DAPI staining and expressed as fold change relative to ethanol-incubated cells. Representative images of the O4 and DAPI staining are presented. Data are presented as mean ± SEM ( n = 5) and were analyzed with one-way ANOVA (with Dunnett’s multiple comparisons test) (* p < 0.05).
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    Image Search Results


    Expression of oligodendrocyte marker O4 by OPCs incubated with H. elongata and S. fusiforme lipid extracts. The surface area percentage of O4 staining, as a marker of pre-oligodendrocytes, was determined on cultured OPCs incubated with lipid extracts of H. elongata and S. fusiforme . The extracts were added based on saringosterol concentration, with a final saringosterol concentration of 0.6 µM. The O4 expression was normalized to the surface area percentage of a DAPI staining and expressed as fold change relative to ethanol-incubated cells. Representative images of the O4 and DAPI staining are presented. Data are presented as mean ± SEM ( n = 5) and were analyzed with one-way ANOVA (with Dunnett’s multiple comparisons test) (* p < 0.05).

    Journal: Nutrients

    Article Title: Supplementation of Seaweed Extracts to the Diet Reduces Symptoms of Alzheimer’s Disease in the APPswePS1ΔE9 Mouse Model

    doi: 10.3390/nu16111614

    Figure Lengend Snippet: Expression of oligodendrocyte marker O4 by OPCs incubated with H. elongata and S. fusiforme lipid extracts. The surface area percentage of O4 staining, as a marker of pre-oligodendrocytes, was determined on cultured OPCs incubated with lipid extracts of H. elongata and S. fusiforme . The extracts were added based on saringosterol concentration, with a final saringosterol concentration of 0.6 µM. The O4 expression was normalized to the surface area percentage of a DAPI staining and expressed as fold change relative to ethanol-incubated cells. Representative images of the O4 and DAPI staining are presented. Data are presented as mean ± SEM ( n = 5) and were analyzed with one-way ANOVA (with Dunnett’s multiple comparisons test) (* p < 0.05).

    Article Snippet: This was followed by a 4 h incubation with a mouse anti-O4 IgM (1:1000; R&D Systems) antibody at room temperature.

    Techniques: Expressing, Marker, Incubation, Staining, Cell Culture, Concentration Assay