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permanent fast red chromogen  (Agilent technologies)


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  • 90

    Structured Review

    Agilent technologies permanent fast red chromogen
    Permanent Fast Red Chromogen, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/permanent+fast+red+chromogen/pm16253968-50-18-22
    Average 90 stars, based on 1 article reviews
    permanent fast red chromogen - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Incubation:

    Article Title: High density of small nerve fibres in the functional layer of the endometrium in women with endometriosis.
    Article Snippet: Serial sections, also cut at 4μm, were immunostained using an antibody for polyclonal rabbit anti-PGP9.5 (dilution 1:700; Dako Cytomation, Sydney, Australia), a highly specific pan-neuronal marker (Lundberg et al., 1988), and monoclonal mouse anti-human NF (dilution 1:200; Dako Cytomation), a highly specific marker for myelinated nerve fibres (Schlaepfer, 1987), for 30min at room temperature. .. Sections were washed in Tris buffer, incubated with Envision-labelled polymer-AP mouse/rabbit for 30min (Dako Cytomation) and stained with permanent fast red chromogen (Dako Cytomation) for 10 min. All immunostaining was carried out on a Dako Autostainer Model S3400 (Dako Cytomation Inc., Carpinteria, CA). .. Images of the sections were captured using an Olympus BX51 digital camera (Olympus, Tokyo, Japan).

    Polymer:

    Article Title: High density of small nerve fibres in the functional layer of the endometrium in women with endometriosis.
    Article Snippet: Serial sections, also cut at 4μm, were immunostained using an antibody for polyclonal rabbit anti-PGP9.5 (dilution 1:700; Dako Cytomation, Sydney, Australia), a highly specific pan-neuronal marker (Lundberg et al., 1988), and monoclonal mouse anti-human NF (dilution 1:200; Dako Cytomation), a highly specific marker for myelinated nerve fibres (Schlaepfer, 1987), for 30min at room temperature. .. Sections were washed in Tris buffer, incubated with Envision-labelled polymer-AP mouse/rabbit for 30min (Dako Cytomation) and stained with permanent fast red chromogen (Dako Cytomation) for 10 min. All immunostaining was carried out on a Dako Autostainer Model S3400 (Dako Cytomation Inc., Carpinteria, CA). .. Images of the sections were captured using an Olympus BX51 digital camera (Olympus, Tokyo, Japan).

    Staining:

    Article Title: High density of small nerve fibres in the functional layer of the endometrium in women with endometriosis.
    Article Snippet: Serial sections, also cut at 4μm, were immunostained using an antibody for polyclonal rabbit anti-PGP9.5 (dilution 1:700; Dako Cytomation, Sydney, Australia), a highly specific pan-neuronal marker (Lundberg et al., 1988), and monoclonal mouse anti-human NF (dilution 1:200; Dako Cytomation), a highly specific marker for myelinated nerve fibres (Schlaepfer, 1987), for 30min at room temperature. .. Sections were washed in Tris buffer, incubated with Envision-labelled polymer-AP mouse/rabbit for 30min (Dako Cytomation) and stained with permanent fast red chromogen (Dako Cytomation) for 10 min. All immunostaining was carried out on a Dako Autostainer Model S3400 (Dako Cytomation Inc., Carpinteria, CA). .. Images of the sections were captured using an Olympus BX51 digital camera (Olympus, Tokyo, Japan).

    Immunostaining:

    Article Title: High density of small nerve fibres in the functional layer of the endometrium in women with endometriosis.
    Article Snippet: Serial sections, also cut at 4μm, were immunostained using an antibody for polyclonal rabbit anti-PGP9.5 (dilution 1:700; Dako Cytomation, Sydney, Australia), a highly specific pan-neuronal marker (Lundberg et al., 1988), and monoclonal mouse anti-human NF (dilution 1:200; Dako Cytomation), a highly specific marker for myelinated nerve fibres (Schlaepfer, 1987), for 30min at room temperature. .. Sections were washed in Tris buffer, incubated with Envision-labelled polymer-AP mouse/rabbit for 30min (Dako Cytomation) and stained with permanent fast red chromogen (Dako Cytomation) for 10 min. All immunostaining was carried out on a Dako Autostainer Model S3400 (Dako Cytomation Inc., Carpinteria, CA). .. Images of the sections were captured using an Olympus BX51 digital camera (Olympus, Tokyo, Japan).



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