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gene protein markers  (Human Protein Atlas)

 
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    Human Protein Atlas gene protein markers
    Gene Protein Markers, supplied by Human Protein Atlas, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gene+protein+markers/clca1+gene+markers+protein/10__31557_slash_apjcp__2026__27__1__163-97-3-20
    Average 86 stars, based on 1 article reviews
    gene protein markers - by Bioz Stars, 2026-09
    86/100 stars

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    other:

    Article Title: Identification and Validation of Prognostic Biomarker Signatures Associated with Overall Survival in Colorectal Cancer: Evidence from Bioinformatics Analysis and an in vivo Study
    Article Snippet: Among the putative gene/protein markers, CLCA1, WNT5A, and CHEK1 showed correlation with overall survival of colorectal cancer patients according to Human Protein Atlas.



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    Gene Protein Markers, supplied by Human Protein Atlas, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    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)
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    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)
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    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)
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    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)
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    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)
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    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)
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    protein levels of marker genes  (Human Protein Atlas)
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    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)
    Protein Levels Of Marker Genes, supplied by Human Protein Atlas, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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