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horseradish peroxidase hrp conjugated donkey polyclonal anti sheep igg  (R&D Systems)


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    R&D Systems horseradish peroxidase hrp conjugated donkey polyclonal anti sheep igg
    Horseradish Peroxidase Hrp Conjugated Donkey Polyclonal Anti Sheep Igg, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 203 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sheep+polyclonal+igg/Sheep+IgG+Horseradish+Peroxidase-conjugated+Antibody/pmc12970870-42-3-13
    Average 95 stars, based on 203 article reviews
    horseradish peroxidase hrp conjugated donkey polyclonal anti sheep igg - by Bioz Stars, 2026-09
    95/100 stars

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    Incubation:

    Article Title: Inhibition of IL34 unveils tissue-selectivity and is sufficient to reduce microglial proliferation in chronic neurodegeneration
    Article Snippet: Mouse myelogenous leukemia (M-NFS-60) cells were M-CSF (R&D systems, 216-MC/CF) starved for 24 hours. .. In white clear bottom 96-well plates 10 μL IL-34 antibody (mouse monoclonal IgG2A (v1.1 manufactured by Genscript, Ma et al., 2012), rat monoclonal IgG2A (MAB5195, R&D Systems) and sheep polyclonal IgG (AF5195, R&D Systems) and 10 μL IL-34 stimulus (R&D systems, 5195-ML-CF) were incubated at 37°C for 30 minutes before 80 μL M-NFS-60 cells (10 3 cells/well) were added. .. After two days incubation at 37°C cell viability was assessed using CellTiterGlo (Promega, G7570) following manufacturer’s instructions.

    Clinical Proteomics:

    Article Title: Inhibition of IL-34 Unveils Tissue-Selectivity and Is Sufficient to Reduce Microglial Proliferation in a Model of Chronic Neurodegeneration
    Article Snippet: .. Mouse myelogenous leukemia (M-NFS-60) cells were CSF-1 (R&D systems, 216-MC/CF) starved for 24 h. In white clear bottom 96-well-plates 10 μL IL-34 antibody (mouse monoclonal IgG2A (v1.1 manufactured by Genscript, ( , )), rat monoclonal IgG2A (MAB5195, R&D Systems) and sheep polyclonal IgG (AF5195, R&D Systems) and 10 μL IL-34 stimulus (R&D systems, 5195-ML-CF) were incubated at 37°C for 30 min before 80 μL M-NFS-60 cells (10 3 cells/well) were added. .. After two days incubation at 37°C cell viability was assessed using CellTiterGlo (Promega, G7570) following manufacturer's instructions.



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    Image Search Results


    Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis of purified WT and X6. The preparations containing 0.6 RUm, 1.2 RUm, 2.4 RUm, and 4.8 RUm of protein (from left to right respective lanes) were loaded on 4% to 12% (gradient) gel and subjected to electrophoresis followed by Coomassie blue staining. Single chain, heavy chain, light chain, A2-A3-C1-C2, and A1/A2 derived correspond to respective FVIII fragments (domains); von Willebrand factor is bovine protein from cell culture medium; S1, a B-domain-FVIII standard (moroctocog alfa); M, molecular weight markers. Multiplicity of heavy chain/light chain bands is related to structural variability (in glycosylation, etc.). The identity of protein bands was confirmed by using anti-FVIII polyclonal antibodies , MS, and a monoclonal anti-A2 antibody (GMA-012). FVIII, factor VIII; RUm, relative units of mass.

    Journal: Research and Practice in Thrombosis and Haemostasis

    Article Title: Mutations of six amino acid residues in a B domain-deleted blood coagulation factor VIII have a cumulative effect on increasing its secretion

    doi: 10.1016/j.rpth.2025.103325

    Figure Lengend Snippet: Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis of purified WT and X6. The preparations containing 0.6 RUm, 1.2 RUm, 2.4 RUm, and 4.8 RUm of protein (from left to right respective lanes) were loaded on 4% to 12% (gradient) gel and subjected to electrophoresis followed by Coomassie blue staining. Single chain, heavy chain, light chain, A2-A3-C1-C2, and A1/A2 derived correspond to respective FVIII fragments (domains); von Willebrand factor is bovine protein from cell culture medium; S1, a B-domain-FVIII standard (moroctocog alfa); M, molecular weight markers. Multiplicity of heavy chain/light chain bands is related to structural variability (in glycosylation, etc.). The identity of protein bands was confirmed by using anti-FVIII polyclonal antibodies , MS, and a monoclonal anti-A2 antibody (GMA-012). FVIII, factor VIII; RUm, relative units of mass.

    Article Snippet: Anti-Human FVIII:C Affinity Purified (Polyclonal) (sheep immunoglobulin [Ig]G) antibodies (CL20035AP) were from Cedarlane Laboratories and mAb GMA-012 (Mab HFVIII R8B12) targeting an epitope on FVIII, formed by residues 497-510 and 584-593, was from Green Mountain Antibodies.

    Techniques: Polyacrylamide Gel Electrophoresis, Purification, Electrophoresis, Staining, Derivative Assay, Cell Culture, Molecular Weight, Glycoproteomics