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cytefinder digital immunofluorescent microscope  (RareCyte Inc)

 
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    Structured Review

    RareCyte Inc cytefinder digital immunofluorescent microscope
    Cytefinder Digital Immunofluorescent Microscope, supplied by RareCyte 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/product/cytefinder+digital+immunofluorescent+microscope/cytefinder+digital+immunofluorescent+microscope/pm40208273-53-6-12
    Average 90 stars, based on 1 article reviews
    cytefinder digital immunofluorescent microscope - by Bioz Stars, 2026-11
    90/100 stars

    Images

    Related Articles

    Staining:

    Article Title: Portal venous circulating tumor cells as a biomarker for relapse prediction in resected pancreatic cancer.
    Article Snippet: Two slides (representing approximately 6 million nucleated cells) were immunofluorescently stained on a Autostainer Link 48 (Dako–Agilent Technologies) using the RarePlex 0700-MA staining kit (RareCyte) comprising a nuclear DAPI dye, anti-pan-cytokeratin (CK) antibody 1 3 155 Page 2 of 12 Portal venous circulating tumor cells as a biomarker for relapse prediction in resected pancreatic cancer conjugated to CF®488, anti-EpCAM antibody conjugated to CF®647, and anti-CD45 antibody conjugated to R-phycoerythrin (PE). .. Stained slides were scanned on the CyteFinder digital immunofluorescent microscope (10X magnification; RareCyte), at exposure times of 0.05s (DAPI), 0.025s (CK), 0.1s (EpCAM), and 0.1s (CD45). .. Image files were analyzed using the CyteMapper® software (RareCyte) and then reviewed by trained users (AB, HS; and confirmation by DY).

    Microscopy:

    Article Title: Portal venous circulating tumor cells as a biomarker for relapse prediction in resected pancreatic cancer.
    Article Snippet: Two slides (representing approximately 6 million nucleated cells) were immunofluorescently stained on a Autostainer Link 48 (Dako–Agilent Technologies) using the RarePlex 0700-MA staining kit (RareCyte) comprising a nuclear DAPI dye, anti-pan-cytokeratin (CK) antibody 1 3 155 Page 2 of 12 Portal venous circulating tumor cells as a biomarker for relapse prediction in resected pancreatic cancer conjugated to CF®488, anti-EpCAM antibody conjugated to CF®647, and anti-CD45 antibody conjugated to R-phycoerythrin (PE). .. Stained slides were scanned on the CyteFinder digital immunofluorescent microscope (10X magnification; RareCyte), at exposure times of 0.05s (DAPI), 0.025s (CK), 0.1s (EpCAM), and 0.1s (CD45). .. Image files were analyzed using the CyteMapper® software (RareCyte) and then reviewed by trained users (AB, HS; and confirmation by DY).



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    RareCyte Inc cytefinder digital immunofluorescent microscope
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    https://www.bioz.com/product/cytefinder+digital+immunofluorescent+microscope/cytefinder+digital+immunofluorescent+microscope/pm40208273-53-6-12
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    RareCyte Inc digital immunofluorescence microscope cytefinder ht
    Representative region of whole-slide immunofluorescence showing circulating tumor cell (CTC, boxed) identified in a GBM patient. Cells were stained for GFAP (green), EGFR (yellow), CD45/CD66b (white) and nuclear DAPI (blue). Magnification, 40X. Sample collected pretreatment (day –9). 7.5 mL peripheral blood was processed on the <t>AccuCyte-CyteFinder</t> platform (RareCyte). Nucleated blood cells were spread on 8 slides. Slides were stained using DAKO autostainer and the whole slide was imaged and analyzed by CyteMapper software for DAPI + GFAP + EGFR + /− CD45/CD66b − cells with user verification. Scale bars = 100 μm.
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    Image Search Results


    Representative region of whole-slide immunofluorescence showing circulating tumor cell (CTC, boxed) identified in a GBM patient. Cells were stained for GFAP (green), EGFR (yellow), CD45/CD66b (white) and nuclear DAPI (blue). Magnification, 40X. Sample collected pretreatment (day –9). 7.5 mL peripheral blood was processed on the AccuCyte-CyteFinder platform (RareCyte). Nucleated blood cells were spread on 8 slides. Slides were stained using DAKO autostainer and the whole slide was imaged and analyzed by CyteMapper software for DAPI + GFAP + EGFR + /− CD45/CD66b − cells with user verification. Scale bars = 100 μm.

    Journal: Nature Medicine

    Article Title: Neoadjuvant triplet immune checkpoint blockade in newly diagnosed glioblastoma

    doi: 10.1038/s41591-025-03512-1

    Figure Lengend Snippet: Representative region of whole-slide immunofluorescence showing circulating tumor cell (CTC, boxed) identified in a GBM patient. Cells were stained for GFAP (green), EGFR (yellow), CD45/CD66b (white) and nuclear DAPI (blue). Magnification, 40X. Sample collected pretreatment (day –9). 7.5 mL peripheral blood was processed on the AccuCyte-CyteFinder platform (RareCyte). Nucleated blood cells were spread on 8 slides. Slides were stained using DAKO autostainer and the whole slide was imaged and analyzed by CyteMapper software for DAPI + GFAP + EGFR + /− CD45/CD66b − cells with user verification. Scale bars = 100 μm.

    Article Snippet: Slides were then scanned on the CyteFinder HT (RareCyte) digital immunofluorescence microscope at ×10 magnification, with the following exposure times: 0.05 s (DAPI); 0.01 s (GFAP); 0.1 s (EGFR); and 0.1 s (CD45/CD66b).

    Techniques: Immunofluorescence, Staining, Software