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reverse capture native protein antigen microarray platform  (Inanovate Inc)

 
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    Inanovate Inc reverse capture native protein antigen microarray platform
    A schematic of the native protein antigen “reverse capture” <t>microarray</t> platform. Well-characterized monoclonal antibodies are printed onto a glass slide. Native protein antigens derived from cell lines or cancer tissues are immobilized onto the array by the printed monoclonal antibodies, with the corresponding antigen captured by a specific monoclonal antibody. Using the immobilized antigens as bait, labeled autoantibodies from a patient and control are then allowed to react with the immobilized antigen. The amount of fluorescent dye-labeled autoantibody between test and control will determine reactivity with the immobilized antigen. We termed this array a “reverse capture” microarray since the standard nomenclature for “capture” refers to the analyte/antigen and not the antibody.
    Reverse Capture Native Protein Antigen Microarray Platform, supplied by Inanovate Inc, 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/result/reverse capture native protein antigen microarray platform/product/Inanovate Inc
    Average 90 stars, based on 1 article reviews
    reverse capture native protein antigen microarray platform - by Bioz Stars, 2026-03
    90/100 stars

    Images

    1) Product Images from "Antibody Profiling with Protein Antigen Microarrays in Early Stage Cancer"

    Article Title: Antibody Profiling with Protein Antigen Microarrays in Early Stage Cancer

    Journal: Expert opinion on medical diagnostics

    doi: 10.1517/17530059.2012.672969

    A schematic of the native protein antigen “reverse capture” microarray platform. Well-characterized monoclonal antibodies are printed onto a glass slide. Native protein antigens derived from cell lines or cancer tissues are immobilized onto the array by the printed monoclonal antibodies, with the corresponding antigen captured by a specific monoclonal antibody. Using the immobilized antigens as bait, labeled autoantibodies from a patient and control are then allowed to react with the immobilized antigen. The amount of fluorescent dye-labeled autoantibody between test and control will determine reactivity with the immobilized antigen. We termed this array a “reverse capture” microarray since the standard nomenclature for “capture” refers to the analyte/antigen and not the antibody.
    Figure Legend Snippet: A schematic of the native protein antigen “reverse capture” microarray platform. Well-characterized monoclonal antibodies are printed onto a glass slide. Native protein antigens derived from cell lines or cancer tissues are immobilized onto the array by the printed monoclonal antibodies, with the corresponding antigen captured by a specific monoclonal antibody. Using the immobilized antigens as bait, labeled autoantibodies from a patient and control are then allowed to react with the immobilized antigen. The amount of fluorescent dye-labeled autoantibody between test and control will determine reactivity with the immobilized antigen. We termed this array a “reverse capture” microarray since the standard nomenclature for “capture” refers to the analyte/antigen and not the antibody.

    Techniques Used: Microarray, Bioprocessing, Derivative Assay, Labeling, Control

    Whole proteome lysate fractionation microarray. Tumor or cell lysates are separated into distinct fractions using a 2-D liquid chromatography fractionation strategy where the 1st dimension is separation by isoelectric points and the 2nd dimension is separation by hydrophobicity. Following the 2nd dimension, the fractions are arrayed onto nitrocellulose coated microscope slides. The slides are then incubated with fluorescent dye-labeled serum antibody isolated from cases and controls. The informative spots on the arrays and their corresponding fractions containing the associated antigens are then validated and the protein antigens subsequently identified by mass spectrometry.
    Figure Legend Snippet: Whole proteome lysate fractionation microarray. Tumor or cell lysates are separated into distinct fractions using a 2-D liquid chromatography fractionation strategy where the 1st dimension is separation by isoelectric points and the 2nd dimension is separation by hydrophobicity. Following the 2nd dimension, the fractions are arrayed onto nitrocellulose coated microscope slides. The slides are then incubated with fluorescent dye-labeled serum antibody isolated from cases and controls. The informative spots on the arrays and their corresponding fractions containing the associated antigens are then validated and the protein antigens subsequently identified by mass spectrometry.

    Techniques Used: Fractionation, Microarray, Liquid Chromatography, Microscopy, Incubation, Labeling, Isolation, Mass Spectrometry

    This figure is an image of a whole proteome breast cancer lysate microarray slide scanned for fluorescence after incubating with antibodies isolated from serum from a patient with late stage breast cancer that have underwent autologous tumor vaccination. Post-vaccination antibodies were labeled with Cy3 (green) fluorescent dye, and pre-vaccination antibodies from the same patient were labeled with Cy5 (red) fluorescent dye. Note that there was little reactivity from the pre-vaccination antibodies, but numerous post-vaccination reactive “spots” are seen.
    Figure Legend Snippet: This figure is an image of a whole proteome breast cancer lysate microarray slide scanned for fluorescence after incubating with antibodies isolated from serum from a patient with late stage breast cancer that have underwent autologous tumor vaccination. Post-vaccination antibodies were labeled with Cy3 (green) fluorescent dye, and pre-vaccination antibodies from the same patient were labeled with Cy5 (red) fluorescent dye. Note that there was little reactivity from the pre-vaccination antibodies, but numerous post-vaccination reactive “spots” are seen.

    Techniques Used: Microarray, Fluorescence, Isolation, Labeling



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    reverse capture native protein antigen microarray platform  (Inanovate Inc)
    90
    Inanovate Inc reverse capture native protein antigen microarray platform
    A schematic of the native protein antigen “reverse capture” <t>microarray</t> platform. Well-characterized monoclonal antibodies are printed onto a glass slide. Native protein antigens derived from cell lines or cancer tissues are immobilized onto the array by the printed monoclonal antibodies, with the corresponding antigen captured by a specific monoclonal antibody. Using the immobilized antigens as bait, labeled autoantibodies from a patient and control are then allowed to react with the immobilized antigen. The amount of fluorescent dye-labeled autoantibody between test and control will determine reactivity with the immobilized antigen. We termed this array a “reverse capture” microarray since the standard nomenclature for “capture” refers to the analyte/antigen and not the antibody.
    Reverse Capture Native Protein Antigen Microarray Platform, supplied by Inanovate Inc, 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/result/reverse capture native protein antigen microarray platform/product/Inanovate Inc
    Average 90 stars, based on 1 article reviews
    reverse capture native protein antigen microarray platform - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    A schematic of the native protein antigen “reverse capture” microarray platform. Well-characterized monoclonal antibodies are printed onto a glass slide. Native protein antigens derived from cell lines or cancer tissues are immobilized onto the array by the printed monoclonal antibodies, with the corresponding antigen captured by a specific monoclonal antibody. Using the immobilized antigens as bait, labeled autoantibodies from a patient and control are then allowed to react with the immobilized antigen. The amount of fluorescent dye-labeled autoantibody between test and control will determine reactivity with the immobilized antigen. We termed this array a “reverse capture” microarray since the standard nomenclature for “capture” refers to the analyte/antigen and not the antibody.

    Journal: Expert opinion on medical diagnostics

    Article Title: Antibody Profiling with Protein Antigen Microarrays in Early Stage Cancer

    doi: 10.1517/17530059.2012.672969

    Figure Lengend Snippet: A schematic of the native protein antigen “reverse capture” microarray platform. Well-characterized monoclonal antibodies are printed onto a glass slide. Native protein antigens derived from cell lines or cancer tissues are immobilized onto the array by the printed monoclonal antibodies, with the corresponding antigen captured by a specific monoclonal antibody. Using the immobilized antigens as bait, labeled autoantibodies from a patient and control are then allowed to react with the immobilized antigen. The amount of fluorescent dye-labeled autoantibody between test and control will determine reactivity with the immobilized antigen. We termed this array a “reverse capture” microarray since the standard nomenclature for “capture” refers to the analyte/antigen and not the antibody.

    Article Snippet: Declaration of interest: Brian Liu serves on the Scientific Advisory Board of Inanovate, Inc., and is one of the inventors and has licensing rights to the “reverse capture” native protein antigen microarray platform described in the article.

    Techniques: Microarray, Bioprocessing, Derivative Assay, Labeling, Control

    Whole proteome lysate fractionation microarray. Tumor or cell lysates are separated into distinct fractions using a 2-D liquid chromatography fractionation strategy where the 1st dimension is separation by isoelectric points and the 2nd dimension is separation by hydrophobicity. Following the 2nd dimension, the fractions are arrayed onto nitrocellulose coated microscope slides. The slides are then incubated with fluorescent dye-labeled serum antibody isolated from cases and controls. The informative spots on the arrays and their corresponding fractions containing the associated antigens are then validated and the protein antigens subsequently identified by mass spectrometry.

    Journal: Expert opinion on medical diagnostics

    Article Title: Antibody Profiling with Protein Antigen Microarrays in Early Stage Cancer

    doi: 10.1517/17530059.2012.672969

    Figure Lengend Snippet: Whole proteome lysate fractionation microarray. Tumor or cell lysates are separated into distinct fractions using a 2-D liquid chromatography fractionation strategy where the 1st dimension is separation by isoelectric points and the 2nd dimension is separation by hydrophobicity. Following the 2nd dimension, the fractions are arrayed onto nitrocellulose coated microscope slides. The slides are then incubated with fluorescent dye-labeled serum antibody isolated from cases and controls. The informative spots on the arrays and their corresponding fractions containing the associated antigens are then validated and the protein antigens subsequently identified by mass spectrometry.

    Article Snippet: Declaration of interest: Brian Liu serves on the Scientific Advisory Board of Inanovate, Inc., and is one of the inventors and has licensing rights to the “reverse capture” native protein antigen microarray platform described in the article.

    Techniques: Fractionation, Microarray, Liquid Chromatography, Microscopy, Incubation, Labeling, Isolation, Mass Spectrometry

    This figure is an image of a whole proteome breast cancer lysate microarray slide scanned for fluorescence after incubating with antibodies isolated from serum from a patient with late stage breast cancer that have underwent autologous tumor vaccination. Post-vaccination antibodies were labeled with Cy3 (green) fluorescent dye, and pre-vaccination antibodies from the same patient were labeled with Cy5 (red) fluorescent dye. Note that there was little reactivity from the pre-vaccination antibodies, but numerous post-vaccination reactive “spots” are seen.

    Journal: Expert opinion on medical diagnostics

    Article Title: Antibody Profiling with Protein Antigen Microarrays in Early Stage Cancer

    doi: 10.1517/17530059.2012.672969

    Figure Lengend Snippet: This figure is an image of a whole proteome breast cancer lysate microarray slide scanned for fluorescence after incubating with antibodies isolated from serum from a patient with late stage breast cancer that have underwent autologous tumor vaccination. Post-vaccination antibodies were labeled with Cy3 (green) fluorescent dye, and pre-vaccination antibodies from the same patient were labeled with Cy5 (red) fluorescent dye. Note that there was little reactivity from the pre-vaccination antibodies, but numerous post-vaccination reactive “spots” are seen.

    Article Snippet: Declaration of interest: Brian Liu serves on the Scientific Advisory Board of Inanovate, Inc., and is one of the inventors and has licensing rights to the “reverse capture” native protein antigen microarray platform described in the article.

    Techniques: Microarray, Fluorescence, Isolation, Labeling