anti-rabbit igg-hrp conjugated secondary antibody Search Results


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  • 99
    Thermo Fisher horseradish peroxidase hrp conjugated secondary antibodies anti rabbit igg hrp
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    Western blot of CTLA-4 expression in porcine PBMC stimulated with CSFV. Proteins from cell lysate were separated by SDS-PAGE gel and transferred to a nitrocellulose membrane. The membrane was probed with human CTLA-4 affinity purified polyclonal antibody and rabbit anti-goat <t>IgG</t> <t>HRP</t> affinity purified antibody. The GAPDH in each sample was amplified as an internal control as shown in the lower panel. Data are representative of three independent experiments.
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    Bio-Rad horseradish peroxidase hrp conjugated anti rabbit igg secondary antibody
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    Vector Laboratories rabbit anti goat igg horseradish peroxidase conjugated secondary antibody
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    Western blot of CTLA-4 expression in porcine PBMC stimulated with CSFV. Proteins from cell lysate were separated by SDS-PAGE gel and transferred to a nitrocellulose membrane. The membrane was probed with human CTLA-4 affinity purified polyclonal antibody and rabbit anti-goat <t>IgG</t> <t>HRP</t> affinity purified antibody. The GAPDH in each sample was amplified as an internal control as shown in the lower panel. Data are representative of three independent experiments.
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    Western blot of CTLA-4 expression in porcine PBMC stimulated with CSFV. Proteins from cell lysate were separated by SDS-PAGE gel and transferred to a nitrocellulose membrane. The membrane was probed with human CTLA-4 affinity purified polyclonal antibody and rabbit anti-goat <t>IgG</t> <t>HRP</t> affinity purified antibody. The GAPDH in each sample was amplified as an internal control as shown in the lower panel. Data are representative of three independent experiments.
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    Santa Cruz Biotechnology goat anti rabbit igg horseradish peroxidase hrp conjugated secondary antibody
    Western blot of CTLA-4 expression in porcine PBMC stimulated with CSFV. Proteins from cell lysate were separated by SDS-PAGE gel and transferred to a nitrocellulose membrane. The membrane was probed with human CTLA-4 affinity purified polyclonal antibody and rabbit anti-goat <t>IgG</t> <t>HRP</t> affinity purified antibody. The GAPDH in each sample was amplified as an internal control as shown in the lower panel. Data are representative of three independent experiments.
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    Jackson Immuno goat anti rabbit igg horseradish peroxidase hrp conjugated secondary antibody
    Western blot of CTLA-4 expression in porcine PBMC stimulated with CSFV. Proteins from cell lysate were separated by SDS-PAGE gel and transferred to a nitrocellulose membrane. The membrane was probed with human CTLA-4 affinity purified polyclonal antibody and rabbit anti-goat <t>IgG</t> <t>HRP</t> affinity purified antibody. The GAPDH in each sample was amplified as an internal control as shown in the lower panel. Data are representative of three independent experiments.
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    Image Search Results


    Western blot of CTLA-4 expression in porcine PBMC stimulated with CSFV. Proteins from cell lysate were separated by SDS-PAGE gel and transferred to a nitrocellulose membrane. The membrane was probed with human CTLA-4 affinity purified polyclonal antibody and rabbit anti-goat IgG HRP affinity purified antibody. The GAPDH in each sample was amplified as an internal control as shown in the lower panel. Data are representative of three independent experiments.

    Journal: PLoS ONE

    Article Title: Effects of Astragalus Polysaccharide on Immune Responses of Porcine PBMC Stimulated with PRRSV or CSFV

    doi: 10.1371/journal.pone.0029320

    Figure Lengend Snippet: Western blot of CTLA-4 expression in porcine PBMC stimulated with CSFV. Proteins from cell lysate were separated by SDS-PAGE gel and transferred to a nitrocellulose membrane. The membrane was probed with human CTLA-4 affinity purified polyclonal antibody and rabbit anti-goat IgG HRP affinity purified antibody. The GAPDH in each sample was amplified as an internal control as shown in the lower panel. Data are representative of three independent experiments.

    Article Snippet: After overnight incubation at 4°C the blots were washed, exposed to secondary antibody rabbit anti-goat IgG HRP (horseradish peroxidase) (R & D Systems, Minneapolis, MN) (dilution 1∶1000) for 1 h, and finally detected by ECL.

    Techniques: Western Blot, Expressing, SDS Page, Affinity Purification, Amplification