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rabbit pan neuronal marker protein gene product  (Bio-Rad)


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    Structured Review

    Bio-Rad rabbit pan neuronal marker protein gene product
    Negative Gb3 immunofluorescence performed on renal sample of Patient 2. ( a ) Negative Gb3 (red); ( b ) Merge of negative Gb3 (red), positive collagen (green), and nuclei (blue). 50-µm sections were prepared using a freezing sliding microtome (HM550, Thermo Scientific, Waltham, MA, USA) to evaluate Gb3 deposits. The sections were immunostained overnight with a panel of primary antibodies, including mouse monoclonal <t>anti-Gb3</t> (1:1000; TCI Chemicals, Portland, Oregon, USA), <t>rabbit</t> <t>pan-neuronal</t> <t>marker</t> <t>protein</t> <t>gene</t> <t>product</t> 9.5 (1:1000; AbD Serotec, Raleigh, NC, USA) and rabbit polyclonal anti-collagen IV (1:500; Novus Biologicals, Littleton, CO, USA). After washing, secondary antibodies were applied for an additional overnight incubation. Mouse cyanine dye fluorophores 3.18 (1:800; Jackson ImmunoResearch, West Grove, PA, USA) were used as secondary antibodies. Sections were viewed and analysed under a Nikon confocal microscopy (Eclipse Ti A1)
    Rabbit Pan Neuronal Marker Protein Gene Product, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 95/100, based on 347 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit pan neuronal marker protein gene product/product/Bio-Rad
    Average 95 stars, based on 347 article reviews
    rabbit pan neuronal marker protein gene product - by Bioz Stars, 2026-05
    95/100 stars

    Images

    1) Product Images from "The importance of a multidisciplinary approach in two tricky cases: the perfect match for Fabry disease"

    Article Title: The importance of a multidisciplinary approach in two tricky cases: the perfect match for Fabry disease

    Journal: BMC Nephrology

    doi: 10.1186/s12882-025-04009-2

    Negative Gb3 immunofluorescence performed on renal sample of Patient 2. ( a ) Negative Gb3 (red); ( b ) Merge of negative Gb3 (red), positive collagen (green), and nuclei (blue). 50-µm sections were prepared using a freezing sliding microtome (HM550, Thermo Scientific, Waltham, MA, USA) to evaluate Gb3 deposits. The sections were immunostained overnight with a panel of primary antibodies, including mouse monoclonal anti-Gb3 (1:1000; TCI Chemicals, Portland, Oregon, USA), rabbit pan-neuronal marker protein gene product 9.5 (1:1000; AbD Serotec, Raleigh, NC, USA) and rabbit polyclonal anti-collagen IV (1:500; Novus Biologicals, Littleton, CO, USA). After washing, secondary antibodies were applied for an additional overnight incubation. Mouse cyanine dye fluorophores 3.18 (1:800; Jackson ImmunoResearch, West Grove, PA, USA) were used as secondary antibodies. Sections were viewed and analysed under a Nikon confocal microscopy (Eclipse Ti A1)
    Figure Legend Snippet: Negative Gb3 immunofluorescence performed on renal sample of Patient 2. ( a ) Negative Gb3 (red); ( b ) Merge of negative Gb3 (red), positive collagen (green), and nuclei (blue). 50-µm sections were prepared using a freezing sliding microtome (HM550, Thermo Scientific, Waltham, MA, USA) to evaluate Gb3 deposits. The sections were immunostained overnight with a panel of primary antibodies, including mouse monoclonal anti-Gb3 (1:1000; TCI Chemicals, Portland, Oregon, USA), rabbit pan-neuronal marker protein gene product 9.5 (1:1000; AbD Serotec, Raleigh, NC, USA) and rabbit polyclonal anti-collagen IV (1:500; Novus Biologicals, Littleton, CO, USA). After washing, secondary antibodies were applied for an additional overnight incubation. Mouse cyanine dye fluorophores 3.18 (1:800; Jackson ImmunoResearch, West Grove, PA, USA) were used as secondary antibodies. Sections were viewed and analysed under a Nikon confocal microscopy (Eclipse Ti A1)

    Techniques Used: Immunofluorescence, Marker, Incubation, Confocal Microscopy



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    Image Search Results


    Negative Gb3 immunofluorescence performed on renal sample of Patient 2. ( a ) Negative Gb3 (red); ( b ) Merge of negative Gb3 (red), positive collagen (green), and nuclei (blue). 50-µm sections were prepared using a freezing sliding microtome (HM550, Thermo Scientific, Waltham, MA, USA) to evaluate Gb3 deposits. The sections were immunostained overnight with a panel of primary antibodies, including mouse monoclonal anti-Gb3 (1:1000; TCI Chemicals, Portland, Oregon, USA), rabbit pan-neuronal marker protein gene product 9.5 (1:1000; AbD Serotec, Raleigh, NC, USA) and rabbit polyclonal anti-collagen IV (1:500; Novus Biologicals, Littleton, CO, USA). After washing, secondary antibodies were applied for an additional overnight incubation. Mouse cyanine dye fluorophores 3.18 (1:800; Jackson ImmunoResearch, West Grove, PA, USA) were used as secondary antibodies. Sections were viewed and analysed under a Nikon confocal microscopy (Eclipse Ti A1)

    Journal: BMC Nephrology

    Article Title: The importance of a multidisciplinary approach in two tricky cases: the perfect match for Fabry disease

    doi: 10.1186/s12882-025-04009-2

    Figure Lengend Snippet: Negative Gb3 immunofluorescence performed on renal sample of Patient 2. ( a ) Negative Gb3 (red); ( b ) Merge of negative Gb3 (red), positive collagen (green), and nuclei (blue). 50-µm sections were prepared using a freezing sliding microtome (HM550, Thermo Scientific, Waltham, MA, USA) to evaluate Gb3 deposits. The sections were immunostained overnight with a panel of primary antibodies, including mouse monoclonal anti-Gb3 (1:1000; TCI Chemicals, Portland, Oregon, USA), rabbit pan-neuronal marker protein gene product 9.5 (1:1000; AbD Serotec, Raleigh, NC, USA) and rabbit polyclonal anti-collagen IV (1:500; Novus Biologicals, Littleton, CO, USA). After washing, secondary antibodies were applied for an additional overnight incubation. Mouse cyanine dye fluorophores 3.18 (1:800; Jackson ImmunoResearch, West Grove, PA, USA) were used as secondary antibodies. Sections were viewed and analysed under a Nikon confocal microscopy (Eclipse Ti A1)

    Article Snippet: The sections were immunostained overnight with a panel of primary antibodies, including mouse monoclonal anti-Gb3 (1:1000; TCI Chemicals, Portland, Oregon, USA), rabbit pan-neuronal marker protein gene product 9.5 (1:1000; AbD Serotec, Raleigh, NC, USA) and rabbit polyclonal anti-collagen IV (1:500; Novus Biologicals, Littleton, CO, USA).

    Techniques: Immunofluorescence, Marker, Incubation, Confocal Microscopy