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mouse monoclonal anti ho1  (Novus Biologicals)


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    Structured Review

    Novus Biologicals mouse monoclonal anti ho1
    Mouse Monoclonal Anti Ho1, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 27 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+monoclonal+anti+ho1/pm32694733-476-5-10?v=Novus+Biologicals
    Average 94 stars, based on 27 article reviews
    mouse monoclonal anti ho1 - by Bioz Stars, 2026-08
    94/100 stars

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    Nordic BioSite mouse monoclonal antibody osa110 anti-ho1
    Western blots showing the effect of curcumin on the induction of the stress response marker heme-oxygenase-1 (HO-1) in mid-passage (less than 50% lifespan completed) human skin fibroblasts ASF-2. The antibody used was a commercially purchased mouse monoclonal antibody anti-HO1 <t>(osa110</t> from Nordic Biosite, Sweden), diluted 1:5000 in PBS containing 1% bovine serum albumin.
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    Image Search Results


    Western blots showing the effect of curcumin on the induction of the stress response marker heme-oxygenase-1 (HO-1) in mid-passage (less than 50% lifespan completed) human skin fibroblasts ASF-2. The antibody used was a commercially purchased mouse monoclonal antibody anti-HO1 (osa110 from Nordic Biosite, Sweden), diluted 1:5000 in PBS containing 1% bovine serum albumin.

    Journal:

    Article Title: Heat Stress and Hormetin-Induced Hormesis in Human Cells: Effects on Aging, Wound Healing, Angiogenesis, and Differentiation

    doi: 10.2203/dose-response.08-014.Rattan

    Figure Lengend Snippet: Western blots showing the effect of curcumin on the induction of the stress response marker heme-oxygenase-1 (HO-1) in mid-passage (less than 50% lifespan completed) human skin fibroblasts ASF-2. The antibody used was a commercially purchased mouse monoclonal antibody anti-HO1 (osa110 from Nordic Biosite, Sweden), diluted 1:5000 in PBS containing 1% bovine serum albumin.

    Article Snippet: The antibodies used in Western blots were commercially purchased mouse monoclonal antibody osa110 anti-HO1, and spa800 for Hsp27 (Nordic Biosite, Sweden), diluted 1:5000 in PBS containing 1% bovine serum albumin. fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIGURE 7 caption a7 Effect of 20 μM rosmarinic acid (RA) treatment for 50 days on senescence markers in late-passage human skin fibroblasts, ASF-2. (A) Light microscopic pictures of ASF2 cells stained for senescence-specific β-galactosidase (microscopic magnification 20x); (B) The proportion of ASF2 cells showing green autofluorescence in FL1 channel.

    Techniques: Western Blot, Marker

    Induction of stress proteins Hsp27 and HO-1 in mid-passage (less than 50% lifespan completed) human skin fibroblasts ASF-2 treated with 20 μM rosmarinic acid (RA) for 72 hr. The antibodies used in Western blots were commercially purchased mouse monoclonal antibody osa110 anti-HO1, and spa800 for Hsp27 (Nordic Biosite, Sweden), diluted 1:5000 in PBS containing 1% bovine serum albumin.

    Journal:

    Article Title: Heat Stress and Hormetin-Induced Hormesis in Human Cells: Effects on Aging, Wound Healing, Angiogenesis, and Differentiation

    doi: 10.2203/dose-response.08-014.Rattan

    Figure Lengend Snippet: Induction of stress proteins Hsp27 and HO-1 in mid-passage (less than 50% lifespan completed) human skin fibroblasts ASF-2 treated with 20 μM rosmarinic acid (RA) for 72 hr. The antibodies used in Western blots were commercially purchased mouse monoclonal antibody osa110 anti-HO1, and spa800 for Hsp27 (Nordic Biosite, Sweden), diluted 1:5000 in PBS containing 1% bovine serum albumin.

    Article Snippet: The antibodies used in Western blots were commercially purchased mouse monoclonal antibody osa110 anti-HO1, and spa800 for Hsp27 (Nordic Biosite, Sweden), diluted 1:5000 in PBS containing 1% bovine serum albumin. fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIGURE 7 caption a7 Effect of 20 μM rosmarinic acid (RA) treatment for 50 days on senescence markers in late-passage human skin fibroblasts, ASF-2. (A) Light microscopic pictures of ASF2 cells stained for senescence-specific β-galactosidase (microscopic magnification 20x); (B) The proportion of ASF2 cells showing green autofluorescence in FL1 channel.

    Techniques: Western Blot