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60 core tissue microarray tma slide  (Novus Biologicals)


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    Structured Review

    Novus Biologicals 60 core tissue microarray tma slide
    60 Core Tissue Microarray Tma Slide, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/microarray+slides/Human+Multi-tissue+Tissue+MicroArray+(Cancer)/pmc13036268-60-45-51
    Average 93 stars, based on 2 article reviews
    60 core tissue microarray tma slide - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Selection:

    Article Title: Techniques to study chimerism at the tissue level in humanized mice
    Article Snippet: As described in previous works, , , rabbit antibodies targeting HLA-A (ab52922, Abcam, Cambridge, Massachusetts; IHC working dilution: 1/600) and human Ku80 (hKu80; 2180; Cell Signaling Technology, Danvers, Massachusetts; IHC working dilution: 1/100), as well as a mouse antibody against a 60 kDa protein on human mitochondria (hMito; MA5-12017; Invitrogen, Waltham, Massachusetts; IHC working dilution: 1/500), were employed as broad-spectrum immunohistochemical markers for identifying virtually all cells of human origin in chimeric mice., , While other broad-spectrum antibodies have been used for this same purpose, including NUMA-1, a comprehensive testing of all the possible markers ubiquitously expressed in human tissues was beyond the scope of this work. .. In this context, the target’s cellular location and distribution were considered in the selection, with HLA-A as a membranous antigen, hKu80 as a nuclear antigen, and hMito as a cytoplasmic marker., , , The overall sensitivity of these 3 broad-spectrum markers was investigated using a 60-core tissue microarray (TMA) slide (NBP2-30233, Novus Biologicals, Centennial, Colorado) containing different types of normal (32 cores) and neoplastic (27 cores) human tissues with one carbon core. ..

    Article Title: Techniques to study chimerism at the tissue level in humanized mice.
    Article Snippet: As described in previous works,6,43,57 rabbit antibodies targeting HLA-A (ab52922, Abcam, Cambridge, Massachusetts; IHC working dilution: 1/600) and human Ku80 (hKu80; 2180; Cell Signaling Technology, Danvers, Massachusetts; IHC working dilution: 1/100), as well as a mouse antibody against a 60 kDa protein on human mitochondria (hMito; MA5-12017; Invitrogen, Waltham, Massachusetts; IHC working dilution: 1/500), were employed as broad-spectrum immunohistochemical markers for identifying virtually all cells of human origin in chimeric mice.9,10,13 While other broad-spectrum antibodies have been used for this same purpose, including NUMA-1,60 a comprehensive testing of all the possible markers ubiquitously expressed in human tissues was beyond the scope of this work. .. In this context, the target’s cellular location and distribution were considered in the selection, with HLA-A as a membranous antigen, hKu80 as a nuclear antigen, and hMito as a cytoplasmic marker.2,6,12,44 The overall sensitivity of these 3 broad-spectrum markers was investigated using a 60-core tissue microarray (TMA) slide (NBP2-30233, Novus Biologicals, Centennial, Colorado) containing different types of normal (32 cores) and neoplastic (27 cores) human tissues with one carbon core. ..

    Marker:

    Article Title: Techniques to study chimerism at the tissue level in humanized mice
    Article Snippet: As described in previous works, , , rabbit antibodies targeting HLA-A (ab52922, Abcam, Cambridge, Massachusetts; IHC working dilution: 1/600) and human Ku80 (hKu80; 2180; Cell Signaling Technology, Danvers, Massachusetts; IHC working dilution: 1/100), as well as a mouse antibody against a 60 kDa protein on human mitochondria (hMito; MA5-12017; Invitrogen, Waltham, Massachusetts; IHC working dilution: 1/500), were employed as broad-spectrum immunohistochemical markers for identifying virtually all cells of human origin in chimeric mice., , While other broad-spectrum antibodies have been used for this same purpose, including NUMA-1, a comprehensive testing of all the possible markers ubiquitously expressed in human tissues was beyond the scope of this work. .. In this context, the target’s cellular location and distribution were considered in the selection, with HLA-A as a membranous antigen, hKu80 as a nuclear antigen, and hMito as a cytoplasmic marker., , , The overall sensitivity of these 3 broad-spectrum markers was investigated using a 60-core tissue microarray (TMA) slide (NBP2-30233, Novus Biologicals, Centennial, Colorado) containing different types of normal (32 cores) and neoplastic (27 cores) human tissues with one carbon core. ..

    Article Title: Techniques to study chimerism at the tissue level in humanized mice.
    Article Snippet: As described in previous works,6,43,57 rabbit antibodies targeting HLA-A (ab52922, Abcam, Cambridge, Massachusetts; IHC working dilution: 1/600) and human Ku80 (hKu80; 2180; Cell Signaling Technology, Danvers, Massachusetts; IHC working dilution: 1/100), as well as a mouse antibody against a 60 kDa protein on human mitochondria (hMito; MA5-12017; Invitrogen, Waltham, Massachusetts; IHC working dilution: 1/500), were employed as broad-spectrum immunohistochemical markers for identifying virtually all cells of human origin in chimeric mice.9,10,13 While other broad-spectrum antibodies have been used for this same purpose, including NUMA-1,60 a comprehensive testing of all the possible markers ubiquitously expressed in human tissues was beyond the scope of this work. .. In this context, the target’s cellular location and distribution were considered in the selection, with HLA-A as a membranous antigen, hKu80 as a nuclear antigen, and hMito as a cytoplasmic marker.2,6,12,44 The overall sensitivity of these 3 broad-spectrum markers was investigated using a 60-core tissue microarray (TMA) slide (NBP2-30233, Novus Biologicals, Centennial, Colorado) containing different types of normal (32 cores) and neoplastic (27 cores) human tissues with one carbon core. ..

    Microarray:

    Article Title: Techniques to study chimerism at the tissue level in humanized mice
    Article Snippet: As described in previous works, , , rabbit antibodies targeting HLA-A (ab52922, Abcam, Cambridge, Massachusetts; IHC working dilution: 1/600) and human Ku80 (hKu80; 2180; Cell Signaling Technology, Danvers, Massachusetts; IHC working dilution: 1/100), as well as a mouse antibody against a 60 kDa protein on human mitochondria (hMito; MA5-12017; Invitrogen, Waltham, Massachusetts; IHC working dilution: 1/500), were employed as broad-spectrum immunohistochemical markers for identifying virtually all cells of human origin in chimeric mice., , While other broad-spectrum antibodies have been used for this same purpose, including NUMA-1, a comprehensive testing of all the possible markers ubiquitously expressed in human tissues was beyond the scope of this work. .. In this context, the target’s cellular location and distribution were considered in the selection, with HLA-A as a membranous antigen, hKu80 as a nuclear antigen, and hMito as a cytoplasmic marker., , , The overall sensitivity of these 3 broad-spectrum markers was investigated using a 60-core tissue microarray (TMA) slide (NBP2-30233, Novus Biologicals, Centennial, Colorado) containing different types of normal (32 cores) and neoplastic (27 cores) human tissues with one carbon core. ..

    Article Title: Techniques to study chimerism at the tissue level in humanized mice.
    Article Snippet: As described in previous works,6,43,57 rabbit antibodies targeting HLA-A (ab52922, Abcam, Cambridge, Massachusetts; IHC working dilution: 1/600) and human Ku80 (hKu80; 2180; Cell Signaling Technology, Danvers, Massachusetts; IHC working dilution: 1/100), as well as a mouse antibody against a 60 kDa protein on human mitochondria (hMito; MA5-12017; Invitrogen, Waltham, Massachusetts; IHC working dilution: 1/500), were employed as broad-spectrum immunohistochemical markers for identifying virtually all cells of human origin in chimeric mice.9,10,13 While other broad-spectrum antibodies have been used for this same purpose, including NUMA-1,60 a comprehensive testing of all the possible markers ubiquitously expressed in human tissues was beyond the scope of this work. .. In this context, the target’s cellular location and distribution were considered in the selection, with HLA-A as a membranous antigen, hKu80 as a nuclear antigen, and hMito as a cytoplasmic marker.2,6,12,44 The overall sensitivity of these 3 broad-spectrum markers was investigated using a 60-core tissue microarray (TMA) slide (NBP2-30233, Novus Biologicals, Centennial, Colorado) containing different types of normal (32 cores) and neoplastic (27 cores) human tissues with one carbon core. ..



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    Novus Biologicals 60 core tissue microarray tma slide
    Mean <t>microarray</t> antigen spot intensities from TB-free badger serum samples at two time points following experimental infection. White bars represent TB-free sera; gray bars represent TB-infected sera collected at ( a ) 8 weeks and ( b ) 12–13 weeks post-infection. Mean microarray spot intensities (log 2 -normalized) are shown with 95% confidence interval error bars. Paired-sample t -tests were carried out comparing pre- and post-infection mean spot intensities. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown. Significance levels: ns: P ≥ 0.05; *: P < 0.05; **: P < 0.01; and ***: P < 0.001.
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    Image Search Results


    Mean microarray antigen spot intensities from TB-free badger serum samples at two time points following experimental infection. White bars represent TB-free sera; gray bars represent TB-infected sera collected at ( a ) 8 weeks and ( b ) 12–13 weeks post-infection. Mean microarray spot intensities (log 2 -normalized) are shown with 95% confidence interval error bars. Paired-sample t -tests were carried out comparing pre- and post-infection mean spot intensities. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown. Significance levels: ns: P ≥ 0.05; *: P < 0.05; **: P < 0.01; and ***: P < 0.001.

    Journal: Journal of Clinical Microbiology

    Article Title: Proteome microarray-guided identification of mycobacterial antigens and ELISA-based peptide mapping for improved serological detection of Mycobacterium bovis infection in European badgers

    doi: 10.1128/jcm.01260-25

    Figure Lengend Snippet: Mean microarray antigen spot intensities from TB-free badger serum samples at two time points following experimental infection. White bars represent TB-free sera; gray bars represent TB-infected sera collected at ( a ) 8 weeks and ( b ) 12–13 weeks post-infection. Mean microarray spot intensities (log 2 -normalized) are shown with 95% confidence interval error bars. Paired-sample t -tests were carried out comparing pre- and post-infection mean spot intensities. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown. Significance levels: ns: P ≥ 0.05; *: P < 0.05; **: P < 0.01; and ***: P < 0.001.

    Article Snippet: Translated proteins and IVTT controls were printed onto custom nitrocellulose-coated microarray slides (Grace Bio-Labs, Bend, OR, USA) using a GeneMachines OmniGrid Accent Microarray Printer.

    Techniques: Microarray, Infection, Comparison

    Mean microarray antigen spot intensities from TB-infected and BCG-vaccinated badger serum samples. Gray bars represent sera from TB-infected badgers collected 12–13 weeks after experimental infection; white bars represent sera from badgers that received ( a ) a single BCG vaccination or ( b ) two BCG vaccinations. Mean spot intensities (log₂-normalized) are shown with 95% confidence interval error bars. Independent-samples t -tests were used to compare antigen intensities between TB-infected and BCG-vaccinated groups. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown; ***: P < 0.001.

    Journal: Journal of Clinical Microbiology

    Article Title: Proteome microarray-guided identification of mycobacterial antigens and ELISA-based peptide mapping for improved serological detection of Mycobacterium bovis infection in European badgers

    doi: 10.1128/jcm.01260-25

    Figure Lengend Snippet: Mean microarray antigen spot intensities from TB-infected and BCG-vaccinated badger serum samples. Gray bars represent sera from TB-infected badgers collected 12–13 weeks after experimental infection; white bars represent sera from badgers that received ( a ) a single BCG vaccination or ( b ) two BCG vaccinations. Mean spot intensities (log₂-normalized) are shown with 95% confidence interval error bars. Independent-samples t -tests were used to compare antigen intensities between TB-infected and BCG-vaccinated groups. Antigens were ranked by BH-adjusted P -values, and the 10 most differential antigens (defined as those with the lowest BH-adjusted P -values) for each comparison group are shown; ***: P < 0.001.

    Article Snippet: Translated proteins and IVTT controls were printed onto custom nitrocellulose-coated microarray slides (Grace Bio-Labs, Bend, OR, USA) using a GeneMachines OmniGrid Accent Microarray Printer.

    Techniques: Microarray, Infection, Comparison