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sheep anti human c3d  (Bio-Rad)


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    Structured Review

    Bio-Rad sheep anti human c3d
    Figure 1 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of SPE B-immunized mice. BALB/c mice were immunized four times with BSA or with 28 kDa SPE B mutant protein C192S (n ¼ 5). (a) Immunoglobulin deposits were detected using HRP-conjugated anti-mouse IgG with light microscopy. (b) Complement C3 deposits were detected using <t>anti-C3d</t> antibody with light microscopy. (c) Using TUNEL assay, cell apoptosis was detected in the valve of SPE B-immunized mice. The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).
    Sheep Anti Human C3d, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 85/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sheep anti human c3d/product/Bio-Rad
    Average 85 stars, based on 2 article reviews
    sheep anti human c3d - by Bioz Stars, 2026-02
    85/100 stars

    Images

    1) Product Images from "Molecular mimicry between streptococcal pyrogenic exotoxin B and endothelial cells."

    Article Title: Molecular mimicry between streptococcal pyrogenic exotoxin B and endothelial cells.

    Journal: Laboratory investigation; a journal of technical methods and pathology

    doi: 10.1038/labinvest.2010.93

    Figure 1 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of SPE B-immunized mice. BALB/c mice were immunized four times with BSA or with 28 kDa SPE B mutant protein C192S (n ¼ 5). (a) Immunoglobulin deposits were detected using HRP-conjugated anti-mouse IgG with light microscopy. (b) Complement C3 deposits were detected using anti-C3d antibody with light microscopy. (c) Using TUNEL assay, cell apoptosis was detected in the valve of SPE B-immunized mice. The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).
    Figure Legend Snippet: Figure 1 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of SPE B-immunized mice. BALB/c mice were immunized four times with BSA or with 28 kDa SPE B mutant protein C192S (n ¼ 5). (a) Immunoglobulin deposits were detected using HRP-conjugated anti-mouse IgG with light microscopy. (b) Complement C3 deposits were detected using anti-C3d antibody with light microscopy. (c) Using TUNEL assay, cell apoptosis was detected in the valve of SPE B-immunized mice. The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).

    Techniques Used: Activation Assay, Mutagenesis, Light Microscopy, TUNEL Assay, Staining

    Figure 3 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of mice after passive immunization with mAb 10G. BALB/c mice were intravenously immunized each day with 500 mg of 9C or mAb 10G for 3 days and, after 7 days, the heart sections were analyzed using HRP- conjugated anti-mouse IgG (a) and anti-C3d antibody (b), and TUNEL assay (c) (n ¼ 3 per group). The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).
    Figure Legend Snippet: Figure 3 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of mice after passive immunization with mAb 10G. BALB/c mice were intravenously immunized each day with 500 mg of 9C or mAb 10G for 3 days and, after 7 days, the heart sections were analyzed using HRP- conjugated anti-mouse IgG (a) and anti-C3d antibody (b), and TUNEL assay (c) (n ¼ 3 per group). The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).

    Techniques Used: Activation Assay, TUNEL Assay, Light Microscopy, Staining



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    Bio-Rad sheep anti human c3d
    Figure 1 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of SPE B-immunized mice. BALB/c mice were immunized four times with BSA or with 28 kDa SPE B mutant protein C192S (n ¼ 5). (a) Immunoglobulin deposits were detected using HRP-conjugated anti-mouse IgG with light microscopy. (b) Complement C3 deposits were detected using <t>anti-C3d</t> antibody with light microscopy. (c) Using TUNEL assay, cell apoptosis was detected in the valve of SPE B-immunized mice. The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).
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    Figure 1 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of SPE B-immunized mice. BALB/c mice were immunized four times with BSA or with 28 kDa SPE B mutant protein C192S (n ¼ 5). (a) Immunoglobulin deposits were detected using HRP-conjugated anti-mouse IgG with light microscopy. (b) Complement C3 deposits were detected using <t>anti-C3d</t> antibody with light microscopy. (c) Using TUNEL assay, cell apoptosis was detected in the valve of SPE B-immunized mice. The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).
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    Image Search Results


    Figure 1 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of SPE B-immunized mice. BALB/c mice were immunized four times with BSA or with 28 kDa SPE B mutant protein C192S (n ¼ 5). (a) Immunoglobulin deposits were detected using HRP-conjugated anti-mouse IgG with light microscopy. (b) Complement C3 deposits were detected using anti-C3d antibody with light microscopy. (c) Using TUNEL assay, cell apoptosis was detected in the valve of SPE B-immunized mice. The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).

    Journal: Laboratory investigation; a journal of technical methods and pathology

    Article Title: Molecular mimicry between streptococcal pyrogenic exotoxin B and endothelial cells.

    doi: 10.1038/labinvest.2010.93

    Figure Lengend Snippet: Figure 1 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of SPE B-immunized mice. BALB/c mice were immunized four times with BSA or with 28 kDa SPE B mutant protein C192S (n ¼ 5). (a) Immunoglobulin deposits were detected using HRP-conjugated anti-mouse IgG with light microscopy. (b) Complement C3 deposits were detected using anti-C3d antibody with light microscopy. (c) Using TUNEL assay, cell apoptosis was detected in the valve of SPE B-immunized mice. The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).

    Article Snippet: Complement C3 was detected using sheep anti-human C3d (Serotec, Oxford, UK), which cross-reacts with mouse C3d, followed by HRP-conjugated goat anti-sheep IgG (Jackson Immunoresearch Laboratories).

    Techniques: Activation Assay, Mutagenesis, Light Microscopy, TUNEL Assay, Staining

    Figure 3 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of mice after passive immunization with mAb 10G. BALB/c mice were intravenously immunized each day with 500 mg of 9C or mAb 10G for 3 days and, after 7 days, the heart sections were analyzed using HRP- conjugated anti-mouse IgG (a) and anti-C3d antibody (b), and TUNEL assay (c) (n ¼ 3 per group). The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).

    Journal: Laboratory investigation; a journal of technical methods and pathology

    Article Title: Molecular mimicry between streptococcal pyrogenic exotoxin B and endothelial cells.

    doi: 10.1038/labinvest.2010.93

    Figure Lengend Snippet: Figure 3 Immunoglobulin deposition, complement activation, and apoptosis in the heart valve of mice after passive immunization with mAb 10G. BALB/c mice were intravenously immunized each day with 500 mg of 9C or mAb 10G for 3 days and, after 7 days, the heart sections were analyzed using HRP- conjugated anti-mouse IgG (a) and anti-C3d antibody (b), and TUNEL assay (c) (n ¼ 3 per group). The visible light microscopy images correspond to the fields showing TUNEL staining (magnification 400).

    Article Snippet: Complement C3 was detected using sheep anti-human C3d (Serotec, Oxford, UK), which cross-reacts with mouse C3d, followed by HRP-conjugated goat anti-sheep IgG (Jackson Immunoresearch Laboratories).

    Techniques: Activation Assay, TUNEL Assay, Light Microscopy, Staining