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nbp1 32440 antibody  (Novus Biologicals)


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    Structured Review

    Novus Biologicals nbp1 32440 antibody
    Nbp1 32440 Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pax8/PAX8+Antibody/pm42011738-106-9-7
    Average 92 stars, based on 11 article reviews
    nbp1 32440 antibody - by Bioz Stars, 2026-09
    92/100 stars

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    Related Articles

    FACS:

    Article Title: Recapitulating thyroid cancer histotypes through engineering embryonic stem cells.
    Article Snippet: DNA content was evaluated by BD FACS Lyric flow cytometer (BD Clinical system, BD Biosciences). .. For FACS analysis, hESCs-derived TPCs were washed in PBS and exposed for 1 h at 4 °C to CD44v6 (2F10 APC, mouse IgG1, R&D systems, 5μl/sample), Oct3/4 (40/Oct-3 Alexa-fluor647, mouse IgG1K, BD Biosciences, 20μl/sample), Sox2 (245610 PE, mouse IgG2a BD Biosciences, 20μl/sample), Nanog (N31-355 PE, mouse IgG1, BD Biosciences, 20μl/sample), CXCR4 (FAB170P PE, mouse IgG2a, R&D system, 1μl/sample), c-kit (YB5.B8 PE, mouse IgG1 BD Biosciences, 20μl/sample), Sox17 (P7-969 PE, mouse IgG1k, BD Biosciences, 5μl/ sample), FoxA2 (N17-280 PE,mouse IgG1, BDBiosciences 5μl/sample), PAX8 (PAX8/1492 APC, mouse IGg2a, Novus 5μl/sample), TTF1 (REA1090 FITC, mouse IgG1, MACS Miltenyi Biotec, 16μl/sample), TSH-R (4C1 FITC, IgG2a Santa Cruz, 2μl/sample), TPO (203340, Antirabbit IgG H + L Alexa-488, Abcam, 2μl/sample), Thyroglobulin (SPM221 PE, mouse IgG1, Novus, 2μl/sample), NIS (SPM186, goat antimouse IgG (H + L) Alexa-488, Abcam, 5μl/sample), CD133 (W6B3C1 FITC, mouse IgG1, BD Bioscience, 20μl/sample), ABCG2 (5D3/CD338 APC, mouse IgG2b, BD Bioscience, 10μl/sample), Nestin (25/Nestin PerCP 5.5, mouse IgG1, BD Bioscience, 5μl/sample), HNF-4α (H-1, goat anti-mouse IgG (H+ L) Alexa-488, Santa Cruz, 4μl/sample), or corresponding isotypematched controls (IMC) and analyzedusing the FACS Lyric cytometer (BD Biosciences). ..

    Article Title: Recapitulating thyroid cancer histotypes through engineering embryonic stem cells
    Article Snippet: DNA content was evaluated by BD FACS Lyric flow cytometer (BD Clinical system, BD Biosciences). .. For FACS analysis, hESCs-derived TPCs were washed in PBS and exposed for 1 h at 4 °C to CD44v6 (2F10 APC, mouse IgG1, R&D systems, 5 μl/sample), Oct3/4 (40/Oct-3 Alexa-fluor647, mouse IgG1K, BD Biosciences, 20 μl/sample), Sox2 (245610 PE, mouse IgG2a BD Biosciences, 20 μl/sample), Nanog (N31-355 PE, mouse IgG1, BD Biosciences, 20 μl/sample), CXCR4 (FAB170P PE, mouse IgG2a, R&D system, 1 μl/sample), c-kit (YB5.B8 PE, mouse IgG1 BD Biosciences, 20 μl/sample), Sox17 (P7-969 PE, mouse IgG1k, BD Biosciences, 5 μl/sample), Fox A2 (N17-280 PE, mouse IgG1, BD Biosciences 5 μl/sample), PAX8 (PAX8/1492 APC, mouse IGg2a, Novus 5 μl/sample), TTF1 (REA1090 FITC, mouse IgG1, MACS Miltenyi Biotec, 16 μl/sample), TSH-R (4C1 FITC, IgG2a Santa Cruz, 2 μl/sample), TPO (203340, Antirabbit IgG H + L Alexa-488, Abcam, 2 μl/sample), Thyroglobulin (SPM221 PE, mouse IgG1, Novus, 2 μl/sample), NIS (SPM186, goat antimouse IgG (H + L) Alexa-488, Abcam, 5 μl/sample), CD133 (W6B3C1 FITC, mouse IgG1, BD Bioscience, 20 μl/sample), ABCG2 (5D3/CD338 APC, mouse IgG2b, BD Bioscience, 10 μl/sample), Nestin (25/Nestin PerCP 5.5, mouse IgG1, BD Bioscience, 5 μl/sample), HNF-4α (H-1, goat anti-mouse IgG (H + L) Alexa-488, Santa Cruz, 4 μl/sample), or corresponding isotype matched controls (IMC) and analyzed using the FACS Lyric cytometer (BD Biosciences). ..

    Magnetic Cell Separation:

    Article Title: Recapitulating thyroid cancer histotypes through engineering embryonic stem cells.
    Article Snippet: DNA content was evaluated by BD FACS Lyric flow cytometer (BD Clinical system, BD Biosciences). .. For FACS analysis, hESCs-derived TPCs were washed in PBS and exposed for 1 h at 4 °C to CD44v6 (2F10 APC, mouse IgG1, R&D systems, 5μl/sample), Oct3/4 (40/Oct-3 Alexa-fluor647, mouse IgG1K, BD Biosciences, 20μl/sample), Sox2 (245610 PE, mouse IgG2a BD Biosciences, 20μl/sample), Nanog (N31-355 PE, mouse IgG1, BD Biosciences, 20μl/sample), CXCR4 (FAB170P PE, mouse IgG2a, R&D system, 1μl/sample), c-kit (YB5.B8 PE, mouse IgG1 BD Biosciences, 20μl/sample), Sox17 (P7-969 PE, mouse IgG1k, BD Biosciences, 5μl/ sample), FoxA2 (N17-280 PE,mouse IgG1, BDBiosciences 5μl/sample), PAX8 (PAX8/1492 APC, mouse IGg2a, Novus 5μl/sample), TTF1 (REA1090 FITC, mouse IgG1, MACS Miltenyi Biotec, 16μl/sample), TSH-R (4C1 FITC, IgG2a Santa Cruz, 2μl/sample), TPO (203340, Antirabbit IgG H + L Alexa-488, Abcam, 2μl/sample), Thyroglobulin (SPM221 PE, mouse IgG1, Novus, 2μl/sample), NIS (SPM186, goat antimouse IgG (H + L) Alexa-488, Abcam, 5μl/sample), CD133 (W6B3C1 FITC, mouse IgG1, BD Bioscience, 20μl/sample), ABCG2 (5D3/CD338 APC, mouse IgG2b, BD Bioscience, 10μl/sample), Nestin (25/Nestin PerCP 5.5, mouse IgG1, BD Bioscience, 5μl/sample), HNF-4α (H-1, goat anti-mouse IgG (H+ L) Alexa-488, Santa Cruz, 4μl/sample), or corresponding isotypematched controls (IMC) and analyzedusing the FACS Lyric cytometer (BD Biosciences). ..

    Article Title: Recapitulating thyroid cancer histotypes through engineering embryonic stem cells
    Article Snippet: .. Flow cytometry analysis: CD44v6 (2F10 APC, mouse IgG1, R&D systems, 5%l/sample), Oct3/4 (40/Oct-3 Alexa-fluor647, mouse IgG1K, BD Biosciences, 20%l/ sample), Sox2 (245610 PE, mouse IgG2a BD Biosciences, 20%l/sample), Nanog (N31-355, mouse IgG1, BD Biosciences, 20%l/sample), CXCR4 (FAB170P PE, mouse IgG2a, R&D system, 1%l/sample), c-kit (YB5.B8 PE, mouse IgG1 BD Biosciences, 20%l/sample), Sox17 (P7-969 PE, mouse IgG1k, BD Biosciences, 5%l/sample), Fox A2 (N17-280 PE, mouse IgG1, BD Biosciences 5%l/sample), PAX8 (PAX8/1492 APC, mouse IGg2a, Novus 5%l/sample), TTF1 (REA1090 FITC, mouse IgG1, MACS Miltenyi Biotec, 16%l/sample), TSH-R (4C1 FITC, IgG2a Santa Cruz, 2%l/sample), TPO (203340, Anti-rabbit IgG H+L Alexa-488, Abcam, 2%l/sample), Thyroglobulin (SPM221 PE, mouse IgG1, Novus, 2%l/sample), NIS (SPM186, goat anti-mouse IgG (H+L) Alexa-488, Abcam, 5%l/sample), CD133 (W6B3C1 FITC, mouse IgG1, BD Bioscience, 20%l/sample), ABCG2 (5D3/CD338 APC, mouse IgG2b, BD Bioscience, 10%l/sample), Nestin (25/Nestin PerCP 5.5, mouse IgG1, BD Bioscience, 5%l/sample), HNF-4" (H-1, goat anti-mouse IgG (H+L) Alexa-488, Santa Cruz, 4%l/sample). .. Immunohistochemistry: Tg (EPR9730, rabbit monoclonal, Abcam, 1:100 dilution), CK19 (B170, mouse IgG1, Leica, 1:50 dilution), #-catenin (E-5, mouse IgG1,k, Santa Cruz, 1:25 dilution), NIS (SPM186, mouse IgG1,k, Abcam, 1:50 dilution), TIMP1 (M7293, mouse IgG1,k, Dako, 1:50 dilution), CD63 (MX-49.129.5, mouse IgG1,k, Santa Cruz, 1:50 dilution), MMP9 (4A3, mouse IgG1, ThermoFisher, 1:100 dilution), CD44v6 (2F10, mouse IgG1, R&D systems, 1:100 dilution), CD44 (156-3c11, mouse monoclonal, Cell Signaling, 1:50), Twist (Twist2C1a, mouse IgG1, Abcam, 1:25 dilution), Snail (63371, rabbit polyclonal, Abcam, 1:50 dilution), KISS1 (34010, rabbit polyclonal, Novus Bio, 1:200 dilution), KISS1R (TA351332, rabbit polyclonal, Origene, 1:50 dilution), TSHR (4C1, mouse IgG2a $, Santa Cruz, 1:50 dilution), S100 (GA504, rabbit polyclonal, Dako, 1:1000 dilution), CDX2 (AMT28, mouse monoclonal IgG1, Novocastra, 1:50 dilution), Oct3/4 (C-10, mouse IgG1, Santa Cruz, 1:200), p40 (PA0163, Leica), P53 (DO-7, mouse monoclonal IgG2b, Novocastra, 1:100 dilution).

    Article Title: Recapitulating thyroid cancer histotypes through engineering embryonic stem cells
    Article Snippet: DNA content was evaluated by BD FACS Lyric flow cytometer (BD Clinical system, BD Biosciences). .. For FACS analysis, hESCs-derived TPCs were washed in PBS and exposed for 1 h at 4 °C to CD44v6 (2F10 APC, mouse IgG1, R&D systems, 5 μl/sample), Oct3/4 (40/Oct-3 Alexa-fluor647, mouse IgG1K, BD Biosciences, 20 μl/sample), Sox2 (245610 PE, mouse IgG2a BD Biosciences, 20 μl/sample), Nanog (N31-355 PE, mouse IgG1, BD Biosciences, 20 μl/sample), CXCR4 (FAB170P PE, mouse IgG2a, R&D system, 1 μl/sample), c-kit (YB5.B8 PE, mouse IgG1 BD Biosciences, 20 μl/sample), Sox17 (P7-969 PE, mouse IgG1k, BD Biosciences, 5 μl/sample), Fox A2 (N17-280 PE, mouse IgG1, BD Biosciences 5 μl/sample), PAX8 (PAX8/1492 APC, mouse IGg2a, Novus 5 μl/sample), TTF1 (REA1090 FITC, mouse IgG1, MACS Miltenyi Biotec, 16 μl/sample), TSH-R (4C1 FITC, IgG2a Santa Cruz, 2 μl/sample), TPO (203340, Antirabbit IgG H + L Alexa-488, Abcam, 2 μl/sample), Thyroglobulin (SPM221 PE, mouse IgG1, Novus, 2 μl/sample), NIS (SPM186, goat antimouse IgG (H + L) Alexa-488, Abcam, 5 μl/sample), CD133 (W6B3C1 FITC, mouse IgG1, BD Bioscience, 20 μl/sample), ABCG2 (5D3/CD338 APC, mouse IgG2b, BD Bioscience, 10 μl/sample), Nestin (25/Nestin PerCP 5.5, mouse IgG1, BD Bioscience, 5 μl/sample), HNF-4α (H-1, goat anti-mouse IgG (H + L) Alexa-488, Santa Cruz, 4 μl/sample), or corresponding isotype matched controls (IMC) and analyzed using the FACS Lyric cytometer (BD Biosciences). ..

    Article Title: Protocol for generation and engineering of thyroid cell lineages using CRISPR-Cas9 editing to recapitulate thyroid cancer histotype progression.
    Article Snippet: Pantina et al., STAR Protocols 5, 103263 September 20, 2024 a 2024 The Author(s).. Published by Thyroid carcinoma represents the first malignancy among the endocrine organs.. Investigating the cellular hierarchy and the mechanisms underlying the initiation of thyroid carcinoma is crucial in thyroid cancer research.

    Cytometry:

    Article Title: Recapitulating thyroid cancer histotypes through engineering embryonic stem cells.
    Article Snippet: DNA content was evaluated by BD FACS Lyric flow cytometer (BD Clinical system, BD Biosciences). .. For FACS analysis, hESCs-derived TPCs were washed in PBS and exposed for 1 h at 4 °C to CD44v6 (2F10 APC, mouse IgG1, R&D systems, 5μl/sample), Oct3/4 (40/Oct-3 Alexa-fluor647, mouse IgG1K, BD Biosciences, 20μl/sample), Sox2 (245610 PE, mouse IgG2a BD Biosciences, 20μl/sample), Nanog (N31-355 PE, mouse IgG1, BD Biosciences, 20μl/sample), CXCR4 (FAB170P PE, mouse IgG2a, R&D system, 1μl/sample), c-kit (YB5.B8 PE, mouse IgG1 BD Biosciences, 20μl/sample), Sox17 (P7-969 PE, mouse IgG1k, BD Biosciences, 5μl/ sample), FoxA2 (N17-280 PE,mouse IgG1, BDBiosciences 5μl/sample), PAX8 (PAX8/1492 APC, mouse IGg2a, Novus 5μl/sample), TTF1 (REA1090 FITC, mouse IgG1, MACS Miltenyi Biotec, 16μl/sample), TSH-R (4C1 FITC, IgG2a Santa Cruz, 2μl/sample), TPO (203340, Antirabbit IgG H + L Alexa-488, Abcam, 2μl/sample), Thyroglobulin (SPM221 PE, mouse IgG1, Novus, 2μl/sample), NIS (SPM186, goat antimouse IgG (H + L) Alexa-488, Abcam, 5μl/sample), CD133 (W6B3C1 FITC, mouse IgG1, BD Bioscience, 20μl/sample), ABCG2 (5D3/CD338 APC, mouse IgG2b, BD Bioscience, 10μl/sample), Nestin (25/Nestin PerCP 5.5, mouse IgG1, BD Bioscience, 5μl/sample), HNF-4α (H-1, goat anti-mouse IgG (H+ L) Alexa-488, Santa Cruz, 4μl/sample), or corresponding isotypematched controls (IMC) and analyzedusing the FACS Lyric cytometer (BD Biosciences). ..

    Article Title: Recapitulating thyroid cancer histotypes through engineering embryonic stem cells
    Article Snippet: DNA content was evaluated by BD FACS Lyric flow cytometer (BD Clinical system, BD Biosciences). .. For FACS analysis, hESCs-derived TPCs were washed in PBS and exposed for 1 h at 4 °C to CD44v6 (2F10 APC, mouse IgG1, R&D systems, 5 μl/sample), Oct3/4 (40/Oct-3 Alexa-fluor647, mouse IgG1K, BD Biosciences, 20 μl/sample), Sox2 (245610 PE, mouse IgG2a BD Biosciences, 20 μl/sample), Nanog (N31-355 PE, mouse IgG1, BD Biosciences, 20 μl/sample), CXCR4 (FAB170P PE, mouse IgG2a, R&D system, 1 μl/sample), c-kit (YB5.B8 PE, mouse IgG1 BD Biosciences, 20 μl/sample), Sox17 (P7-969 PE, mouse IgG1k, BD Biosciences, 5 μl/sample), Fox A2 (N17-280 PE, mouse IgG1, BD Biosciences 5 μl/sample), PAX8 (PAX8/1492 APC, mouse IGg2a, Novus 5 μl/sample), TTF1 (REA1090 FITC, mouse IgG1, MACS Miltenyi Biotec, 16 μl/sample), TSH-R (4C1 FITC, IgG2a Santa Cruz, 2 μl/sample), TPO (203340, Antirabbit IgG H + L Alexa-488, Abcam, 2 μl/sample), Thyroglobulin (SPM221 PE, mouse IgG1, Novus, 2 μl/sample), NIS (SPM186, goat antimouse IgG (H + L) Alexa-488, Abcam, 5 μl/sample), CD133 (W6B3C1 FITC, mouse IgG1, BD Bioscience, 20 μl/sample), ABCG2 (5D3/CD338 APC, mouse IgG2b, BD Bioscience, 10 μl/sample), Nestin (25/Nestin PerCP 5.5, mouse IgG1, BD Bioscience, 5 μl/sample), HNF-4α (H-1, goat anti-mouse IgG (H + L) Alexa-488, Santa Cruz, 4 μl/sample), or corresponding isotype matched controls (IMC) and analyzed using the FACS Lyric cytometer (BD Biosciences). ..

    Flow Cytometry:

    Article Title: Recapitulating thyroid cancer histotypes through engineering embryonic stem cells
    Article Snippet: .. Flow cytometry analysis: CD44v6 (2F10 APC, mouse IgG1, R&D systems, 5%l/sample), Oct3/4 (40/Oct-3 Alexa-fluor647, mouse IgG1K, BD Biosciences, 20%l/ sample), Sox2 (245610 PE, mouse IgG2a BD Biosciences, 20%l/sample), Nanog (N31-355, mouse IgG1, BD Biosciences, 20%l/sample), CXCR4 (FAB170P PE, mouse IgG2a, R&D system, 1%l/sample), c-kit (YB5.B8 PE, mouse IgG1 BD Biosciences, 20%l/sample), Sox17 (P7-969 PE, mouse IgG1k, BD Biosciences, 5%l/sample), Fox A2 (N17-280 PE, mouse IgG1, BD Biosciences 5%l/sample), PAX8 (PAX8/1492 APC, mouse IGg2a, Novus 5%l/sample), TTF1 (REA1090 FITC, mouse IgG1, MACS Miltenyi Biotec, 16%l/sample), TSH-R (4C1 FITC, IgG2a Santa Cruz, 2%l/sample), TPO (203340, Anti-rabbit IgG H+L Alexa-488, Abcam, 2%l/sample), Thyroglobulin (SPM221 PE, mouse IgG1, Novus, 2%l/sample), NIS (SPM186, goat anti-mouse IgG (H+L) Alexa-488, Abcam, 5%l/sample), CD133 (W6B3C1 FITC, mouse IgG1, BD Bioscience, 20%l/sample), ABCG2 (5D3/CD338 APC, mouse IgG2b, BD Bioscience, 10%l/sample), Nestin (25/Nestin PerCP 5.5, mouse IgG1, BD Bioscience, 5%l/sample), HNF-4" (H-1, goat anti-mouse IgG (H+L) Alexa-488, Santa Cruz, 4%l/sample). .. Immunohistochemistry: Tg (EPR9730, rabbit monoclonal, Abcam, 1:100 dilution), CK19 (B170, mouse IgG1, Leica, 1:50 dilution), #-catenin (E-5, mouse IgG1,k, Santa Cruz, 1:25 dilution), NIS (SPM186, mouse IgG1,k, Abcam, 1:50 dilution), TIMP1 (M7293, mouse IgG1,k, Dako, 1:50 dilution), CD63 (MX-49.129.5, mouse IgG1,k, Santa Cruz, 1:50 dilution), MMP9 (4A3, mouse IgG1, ThermoFisher, 1:100 dilution), CD44v6 (2F10, mouse IgG1, R&D systems, 1:100 dilution), CD44 (156-3c11, mouse monoclonal, Cell Signaling, 1:50), Twist (Twist2C1a, mouse IgG1, Abcam, 1:25 dilution), Snail (63371, rabbit polyclonal, Abcam, 1:50 dilution), KISS1 (34010, rabbit polyclonal, Novus Bio, 1:200 dilution), KISS1R (TA351332, rabbit polyclonal, Origene, 1:50 dilution), TSHR (4C1, mouse IgG2a $, Santa Cruz, 1:50 dilution), S100 (GA504, rabbit polyclonal, Dako, 1:1000 dilution), CDX2 (AMT28, mouse monoclonal IgG1, Novocastra, 1:50 dilution), Oct3/4 (C-10, mouse IgG1, Santa Cruz, 1:200), p40 (PA0163, Leica), P53 (DO-7, mouse monoclonal IgG2b, Novocastra, 1:100 dilution).

    Isolation:

    Article Title: Rewiring of master transcription factor cistromes during high-grade serous ovarian cancer development
    Article Snippet: CUT&RUN was performed based on the CUTANA CUT&RUN protocol v1.6 (Epicypher). .. Isolated nuclei from FT282 and KURAMOCHI were bound to Concalavin A beads and incubated overnight at 4°C with primary antibody for H3K27me3 (Cell Signaling, RRID:AB_2798370), H3K27ac (Diagenode, RRID:AB_2637079), MECOM (Cell Signaling, AB_2184098), PAX8 (Novus, RRID:AB_2283498), SOX17 (Abcam, RRID:AB_2801385), WT1 (Santa Cruz, RRID:AB_632611). ..

    Incubation:

    Article Title: Rewiring of master transcription factor cistromes during high-grade serous ovarian cancer development
    Article Snippet: CUT&RUN was performed based on the CUTANA CUT&RUN protocol v1.6 (Epicypher). .. Isolated nuclei from FT282 and KURAMOCHI were bound to Concalavin A beads and incubated overnight at 4°C with primary antibody for H3K27me3 (Cell Signaling, RRID:AB_2798370), H3K27ac (Diagenode, RRID:AB_2637079), MECOM (Cell Signaling, AB_2184098), PAX8 (Novus, RRID:AB_2283498), SOX17 (Abcam, RRID:AB_2801385), WT1 (Santa Cruz, RRID:AB_632611). ..

    Article Title: Role of GLIS3 in thyroid development and in the regulation of gene expression in thyroid specific Glis3KO mice
    Article Snippet: .. Frozen sections (10 μm) were obtained using a cryostat (Leica Biosystems, Deer Park, IL) and subsequently immunostained with either a GFP (A-11122, Life Technology or GFP1010, Aves Labs), PAX8 (NBP1-32440, Novus Biologicals), NKX2.1 (ab76013, Abcam), CDH16 (PA557589, ThermoFisher), ZO-1 (61-7300, ThermoFisher), E-Cadherin (CDH1; U3254, Sigma-Aldrich), PECAM1 (#550274, BD Pharmingen, San Diego, CA), pRPS6 (#2211, Cell Signaling), pan collagen (PA1-36058, ThermoFisher) or SLC5A5 (gift from Dr. N. Carrasco) antibody and then incubated with Alexa Fluor 488- or 594-conjugated secondary antibodies (ThermoFisher) for 1 h at room temperature. .. Wheat germ agglutinin (WGA) conjugated with Alexa Fluor 647 was used to stain cell membrane and nuclei with DAPI Prolong Diamond (both from ThermoFisher).



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    A) Anti-human IgG (left) immunohistochemistry (IHC) staining of an HGSOC primary solid tumor specimen from patient 9. <t>Anti-PAX8</t> staining (right) is included as a tumor-specific lineage marker. Scale bars represent 50 µm or 100 µm, where noted. B) Anti-human IgG (top) IHC staining of an HGSOC ascites specimen from patient 56. Anti-PAX8 staining (bottom) of the same ascites specimen from patient 56. Scale bars represent 50 µm or 100 µm, where noted. C) Quantification of the staining across patients with available samples in the cohort (n=29). Samples with heterogeneous staining were assigned a range instead of a single score. D) Visual depiction of our hypothesis. While TBAs bind to tumor cells, their Fc properties may prevent interaction with the FcγRs on immune cells. E) The ratio of FcγRIIIa to FcγRIIa binding across patients, separated by Ab antigenic target (n=61). Fluorescence is indicated by relative fluorescence units (RFU). In E), significance was determined between the TBAs and anti-viral Abs using a Kruskal-Wallis H Test followed by Dunn’s post-hoc test with Bonferroni corrections. Here, “*” and “**” represent p-values of less than 0.05 and 0.0005, respectively. See also Figure S1 and Table S1.
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    A) Anti-human IgG (left) immunohistochemistry (IHC) staining of an HGSOC primary solid tumor specimen from patient 9. <t>Anti-PAX8</t> staining (right) is included as a tumor-specific lineage marker. Scale bars represent 50 µm or 100 µm, where noted. B) Anti-human IgG (top) IHC staining of an HGSOC ascites specimen from patient 56. Anti-PAX8 staining (bottom) of the same ascites specimen from patient 56. Scale bars represent 50 µm or 100 µm, where noted. C) Quantification of the staining across patients with available samples in the cohort (n=29). Samples with heterogeneous staining were assigned a range instead of a single score. D) Visual depiction of our hypothesis. While TBAs bind to tumor cells, their Fc properties may prevent interaction with the FcγRs on immune cells. E) The ratio of FcγRIIIa to FcγRIIa binding across patients, separated by Ab antigenic target (n=61). Fluorescence is indicated by relative fluorescence units (RFU). In E), significance was determined between the TBAs and anti-viral Abs using a Kruskal-Wallis H Test followed by Dunn’s post-hoc test with Bonferroni corrections. Here, “*” and “**” represent p-values of less than 0.05 and 0.0005, respectively. See also Figure S1 and Table S1.
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    A) Anti-human IgG (left) immunohistochemistry (IHC) staining of an HGSOC primary solid tumor specimen from patient 9. <t>Anti-PAX8</t> staining (right) is included as a tumor-specific lineage marker. Scale bars represent 50 µm or 100 µm, where noted. B) Anti-human IgG (top) IHC staining of an HGSOC ascites specimen from patient 56. Anti-PAX8 staining (bottom) of the same ascites specimen from patient 56. Scale bars represent 50 µm or 100 µm, where noted. C) Quantification of the staining across patients with available samples in the cohort (n=29). Samples with heterogeneous staining were assigned a range instead of a single score. D) Visual depiction of our hypothesis. While TBAs bind to tumor cells, their Fc properties may prevent interaction with the FcγRs on immune cells. E) The ratio of FcγRIIIa to FcγRIIa binding across patients, separated by Ab antigenic target (n=61). Fluorescence is indicated by relative fluorescence units (RFU). In E), significance was determined between the TBAs and anti-viral Abs using a Kruskal-Wallis H Test followed by Dunn’s post-hoc test with Bonferroni corrections. Here, “*” and “**” represent p-values of less than 0.05 and 0.0005, respectively. See also Figure S1 and Table S1.
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    A) Anti-human IgG (left) immunohistochemistry (IHC) staining of an HGSOC primary solid tumor specimen from patient 9. <t>Anti-PAX8</t> staining (right) is included as a tumor-specific lineage marker. Scale bars represent 50 µm or 100 µm, where noted. B) Anti-human IgG (top) IHC staining of an HGSOC ascites specimen from patient 56. Anti-PAX8 staining (bottom) of the same ascites specimen from patient 56. Scale bars represent 50 µm or 100 µm, where noted. C) Quantification of the staining across patients with available samples in the cohort (n=29). Samples with heterogeneous staining were assigned a range instead of a single score. D) Visual depiction of our hypothesis. While TBAs bind to tumor cells, their Fc properties may prevent interaction with the FcγRs on immune cells. E) The ratio of FcγRIIIa to FcγRIIa binding across patients, separated by Ab antigenic target (n=61). Fluorescence is indicated by relative fluorescence units (RFU). In E), significance was determined between the TBAs and anti-viral Abs using a Kruskal-Wallis H Test followed by Dunn’s post-hoc test with Bonferroni corrections. Here, “*” and “**” represent p-values of less than 0.05 and 0.0005, respectively. See also Figure S1 and Table S1.
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    Image Search Results


    A) Anti-human IgG (left) immunohistochemistry (IHC) staining of an HGSOC primary solid tumor specimen from patient 9. Anti-PAX8 staining (right) is included as a tumor-specific lineage marker. Scale bars represent 50 µm or 100 µm, where noted. B) Anti-human IgG (top) IHC staining of an HGSOC ascites specimen from patient 56. Anti-PAX8 staining (bottom) of the same ascites specimen from patient 56. Scale bars represent 50 µm or 100 µm, where noted. C) Quantification of the staining across patients with available samples in the cohort (n=29). Samples with heterogeneous staining were assigned a range instead of a single score. D) Visual depiction of our hypothesis. While TBAs bind to tumor cells, their Fc properties may prevent interaction with the FcγRs on immune cells. E) The ratio of FcγRIIIa to FcγRIIa binding across patients, separated by Ab antigenic target (n=61). Fluorescence is indicated by relative fluorescence units (RFU). In E), significance was determined between the TBAs and anti-viral Abs using a Kruskal-Wallis H Test followed by Dunn’s post-hoc test with Bonferroni corrections. Here, “*” and “**” represent p-values of less than 0.05 and 0.0005, respectively. See also Figure S1 and Table S1.

    Journal: bioRxiv

    Article Title: Systems serology of responses against tumor antigens in ovarian cancer reveal disrupted Fc-mediated immunity

    doi: 10.64898/2026.04.25.720834

    Figure Lengend Snippet: A) Anti-human IgG (left) immunohistochemistry (IHC) staining of an HGSOC primary solid tumor specimen from patient 9. Anti-PAX8 staining (right) is included as a tumor-specific lineage marker. Scale bars represent 50 µm or 100 µm, where noted. B) Anti-human IgG (top) IHC staining of an HGSOC ascites specimen from patient 56. Anti-PAX8 staining (bottom) of the same ascites specimen from patient 56. Scale bars represent 50 µm or 100 µm, where noted. C) Quantification of the staining across patients with available samples in the cohort (n=29). Samples with heterogeneous staining were assigned a range instead of a single score. D) Visual depiction of our hypothesis. While TBAs bind to tumor cells, their Fc properties may prevent interaction with the FcγRs on immune cells. E) The ratio of FcγRIIIa to FcγRIIa binding across patients, separated by Ab antigenic target (n=61). Fluorescence is indicated by relative fluorescence units (RFU). In E), significance was determined between the TBAs and anti-viral Abs using a Kruskal-Wallis H Test followed by Dunn’s post-hoc test with Bonferroni corrections. Here, “*” and “**” represent p-values of less than 0.05 and 0.0005, respectively. See also Figure S1 and Table S1.

    Article Snippet: Sections were incubated in blocking buffer and stained with the following antibodies: PAX8 (Cell Marque #363M-15) and IgG (Dako #GA512).

    Techniques: Immunohistochemistry, Staining, Marker, Binding Assay, Fluorescence