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human thyroid cancer tissue array  (Novus Biologicals)


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    Novus Biologicals human thyroid cancer tissue array
    Figure 2 Immunohistochemistry with anti-PPARg antibody. Except for four frozen FTC <t>tumor</t> sections, all tissues were paraffin embedded and most were analysed as components of <t>tissue</t> microarrays. Normal <t>thyroid</t> sections were included in each experiment as positive controls. Following dewaxing with xylene and antigen retrieval in citric acid buffer for 30 min at 941C, the PPARg (E8) mouse monoclonal antibody (sc-7273, Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA) was incubated at a dilution of one in 12 for 1 h at 371C. Detection was by the LSAB2 streptavidin-horseradish peroxidase system (DAKO Corp., Car- pinteria, CA, USA) and counterstaining with hematoxylin l. Slides were scored for the presence or absence of nuclear staining and the intensity of staining was compared to the normal control from the same experiment. (a) normal thyroid shows moderate staining in the nucleus; (b) FTC with complete absence of staining; and (c) translocation-positive FTC shows very strong nuclear staining
    Human Thyroid Cancer Tissue Array, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human thyroid cancer tissue array/product/Novus Biologicals
    Average 90 stars, based on 4 article reviews
    human thyroid cancer tissue array - by Bioz Stars, 2026-05
    90/100 stars

    Images

    1) Product Images from "Peroxisome proliferator-activated receptor gamma is frequently downregulated in a diversity of sporadic nonmedullary thyroid carcinomas."

    Article Title: Peroxisome proliferator-activated receptor gamma is frequently downregulated in a diversity of sporadic nonmedullary thyroid carcinomas.

    Journal: Oncogene

    doi: 10.1038/sj.onc.1206400

    Figure 2 Immunohistochemistry with anti-PPARg antibody. Except for four frozen FTC tumor sections, all tissues were paraffin embedded and most were analysed as components of tissue microarrays. Normal thyroid sections were included in each experiment as positive controls. Following dewaxing with xylene and antigen retrieval in citric acid buffer for 30 min at 941C, the PPARg (E8) mouse monoclonal antibody (sc-7273, Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA) was incubated at a dilution of one in 12 for 1 h at 371C. Detection was by the LSAB2 streptavidin-horseradish peroxidase system (DAKO Corp., Car- pinteria, CA, USA) and counterstaining with hematoxylin l. Slides were scored for the presence or absence of nuclear staining and the intensity of staining was compared to the normal control from the same experiment. (a) normal thyroid shows moderate staining in the nucleus; (b) FTC with complete absence of staining; and (c) translocation-positive FTC shows very strong nuclear staining
    Figure Legend Snippet: Figure 2 Immunohistochemistry with anti-PPARg antibody. Except for four frozen FTC tumor sections, all tissues were paraffin embedded and most were analysed as components of tissue microarrays. Normal thyroid sections were included in each experiment as positive controls. Following dewaxing with xylene and antigen retrieval in citric acid buffer for 30 min at 941C, the PPARg (E8) mouse monoclonal antibody (sc-7273, Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA) was incubated at a dilution of one in 12 for 1 h at 371C. Detection was by the LSAB2 streptavidin-horseradish peroxidase system (DAKO Corp., Car- pinteria, CA, USA) and counterstaining with hematoxylin l. Slides were scored for the presence or absence of nuclear staining and the intensity of staining was compared to the normal control from the same experiment. (a) normal thyroid shows moderate staining in the nucleus; (b) FTC with complete absence of staining; and (c) translocation-positive FTC shows very strong nuclear staining

    Techniques Used: Immunohistochemistry, Incubation, Staining, Control, Translocation Assay



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    Novus Biologicals human thyroid cancer tissue array
    Figure 2 Immunohistochemistry with anti-PPARg antibody. Except for four frozen FTC <t>tumor</t> sections, all tissues were paraffin embedded and most were analysed as components of <t>tissue</t> microarrays. Normal <t>thyroid</t> sections were included in each experiment as positive controls. Following dewaxing with xylene and antigen retrieval in citric acid buffer for 30 min at 941C, the PPARg (E8) mouse monoclonal antibody (sc-7273, Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA) was incubated at a dilution of one in 12 for 1 h at 371C. Detection was by the LSAB2 streptavidin-horseradish peroxidase system (DAKO Corp., Car- pinteria, CA, USA) and counterstaining with hematoxylin l. Slides were scored for the presence or absence of nuclear staining and the intensity of staining was compared to the normal control from the same experiment. (a) normal thyroid shows moderate staining in the nucleus; (b) FTC with complete absence of staining; and (c) translocation-positive FTC shows very strong nuclear staining
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    https://www.bioz.com/result/human thyroid cancer tissue array/product/Novus Biologicals
    Average 90 stars, based on 1 article reviews
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    Image Search Results


    Figure 2 Immunohistochemistry with anti-PPARg antibody. Except for four frozen FTC tumor sections, all tissues were paraffin embedded and most were analysed as components of tissue microarrays. Normal thyroid sections were included in each experiment as positive controls. Following dewaxing with xylene and antigen retrieval in citric acid buffer for 30 min at 941C, the PPARg (E8) mouse monoclonal antibody (sc-7273, Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA) was incubated at a dilution of one in 12 for 1 h at 371C. Detection was by the LSAB2 streptavidin-horseradish peroxidase system (DAKO Corp., Car- pinteria, CA, USA) and counterstaining with hematoxylin l. Slides were scored for the presence or absence of nuclear staining and the intensity of staining was compared to the normal control from the same experiment. (a) normal thyroid shows moderate staining in the nucleus; (b) FTC with complete absence of staining; and (c) translocation-positive FTC shows very strong nuclear staining

    Journal: Oncogene

    Article Title: Peroxisome proliferator-activated receptor gamma is frequently downregulated in a diversity of sporadic nonmedullary thyroid carcinomas.

    doi: 10.1038/sj.onc.1206400

    Figure Lengend Snippet: Figure 2 Immunohistochemistry with anti-PPARg antibody. Except for four frozen FTC tumor sections, all tissues were paraffin embedded and most were analysed as components of tissue microarrays. Normal thyroid sections were included in each experiment as positive controls. Following dewaxing with xylene and antigen retrieval in citric acid buffer for 30 min at 941C, the PPARg (E8) mouse monoclonal antibody (sc-7273, Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA) was incubated at a dilution of one in 12 for 1 h at 371C. Detection was by the LSAB2 streptavidin-horseradish peroxidase system (DAKO Corp., Car- pinteria, CA, USA) and counterstaining with hematoxylin l. Slides were scored for the presence or absence of nuclear staining and the intensity of staining was compared to the normal control from the same experiment. (a) normal thyroid shows moderate staining in the nucleus; (b) FTC with complete absence of staining; and (c) translocation-positive FTC shows very strong nuclear staining

    Article Snippet: A total of 142 sections were analysed, as detailed in Table 1b, including 17 of the 19 FTCs used for RT–PCR analysis, additional independent cases accrued through the Department of Pathology, The Ohio State University and a commercial human thyroid cancer tissue array (Imgenex IMH-319).

    Techniques: Immunohistochemistry, Incubation, Staining, Control, Translocation Assay