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microarray scanner  (Danaher Inc)


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    Danaher Inc microarray scanner
    Microarray Scanner, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 94/100, based on 461 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/Microarrays/GenePix+Microarray+Systems/pm42772593-192-17-19
    Average 94 stars, based on 461 article reviews
    microarray scanner - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Formalin-fixed Paraffin-Embedded:

    Article Title: Identification of Proteomic Features To Distinguish Benign Pulmonary Nodules from Lung Adenocarcinoma.
    Article Snippet: .. Five micron tissue sections were cut from FFPE lung tissue microarrays were placed on the Leica Bond Max IHC stainer (Leica Biosystems, Buffalo Grove, IL). ..

    Immunohistochemistry:

    Article Title: Identification of Proteomic Features To Distinguish Benign Pulmonary Nodules from Lung Adenocarcinoma.
    Article Snippet: .. Five micron tissue sections were cut from FFPE lung tissue microarrays were placed on the Leica Bond Max IHC stainer (Leica Biosystems, Buffalo Grove, IL). ..

    Staining:

    Article Title: Presence of regulatory T-cells in endometrial cancer predicts poorer overall survival and promotes progression of tumor cells
    Article Snippet: .. Paraffin-embedded tissue microarrays (TMA, surface 0.785 mm 2 each spot) of 275 patients with EC were stained with a mouse anti-FoxP3 antibody (Dilution 1:300; ab 20,034, Abcam, Cambridge, UK) using ZytoChem Plus HRP Polymer System mouse/rabbit (Zytomed, Berlin, Germany) in accordance with the manufacturer’s instructions. .. 3,3-diaminobenzidine (DAKO DAB + ; Agilent technologies, Santa Clara, CA, USA) was used as chromogen.

    Polymer:

    Article Title: Presence of regulatory T-cells in endometrial cancer predicts poorer overall survival and promotes progression of tumor cells
    Article Snippet: .. Paraffin-embedded tissue microarrays (TMA, surface 0.785 mm 2 each spot) of 275 patients with EC were stained with a mouse anti-FoxP3 antibody (Dilution 1:300; ab 20,034, Abcam, Cambridge, UK) using ZytoChem Plus HRP Polymer System mouse/rabbit (Zytomed, Berlin, Germany) in accordance with the manufacturer’s instructions. .. 3,3-diaminobenzidine (DAKO DAB + ; Agilent technologies, Santa Clara, CA, USA) was used as chromogen.

    other:

    Article Title: Factor XIIIA—expressing inflammatory monocytes promote lung squamous cancer through fibrin cross-linking
    Article Snippet: Working with UNC’s tissue pathology laboratory, the tissue microarrays were stained for CD14 (Leica Biosystems: mouse monoclonal anti-human CD14, #NCL-L-CD14-223, clone 7) and cross-linked fibrin (Zedira, mouse anti-human cross-linked fibrin, A076, 1:1,500 dilution).

    Chromatin Immunoprecipitation:

    Article Title: Genome-wide profiling of nardilysin target genes reveals its role in epigenetic regulation and cell cycle progression
    Article Snippet: Fragmented libraries were created using the NEBNext Fast DNA Library Prep Set for the Ion Torrent kit (New England Biolabs) according to manufacturer’s protocol with slight modifications. .. Briefly, ChIP DNA was end-repaired, adapter-ligated, and size-selected with Agencourt AMPure XP (Beckman Coulter Inc.) to 150–350 bp in length. .. DNA was PCR amplified with the Ion barcode adapter (Thermo Fischer Inc.) for 12 cycles.



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    Image Search Results


    BNT351 shows comparable target affinity to 1-18 and no off-target binding (A) Left: the binding affinity of BNT351 and 1-18 to the stabilized HIV-1 envelope protein trimer (SOSIP BG505.664 ) by SPR (mean and individual values of triplicate measurements). Also see A. Right: binding of BNT351 and 1-18 to SOSIP BG505.664 by ELISA (mean ± standard deviation of triplicate measurements). (B) BNT351’s off-target binding was assessed by Retrogenix Cell Microarray Technology platform. Interactions identified during the library screen with ∼6,500 human proteins are shown. Also, see . Interaction with pepsinogen C (PGC) that appeared to be specific was re-tested by flow cytometry with HEK293 cells transfected with PGC. HEK293 cells transfected with FcγRIIIa and FcεRIg were used as a positive control. Duplicate measurements are shown for flow cytometry.

    Journal: iScience

    Article Title: Preclinical assessment of broadly neutralizing HIV-1 antibody BNT351 with optimized pharmacokinetics and potent antiviral activity

    doi: 10.1016/j.isci.2026.116022

    Figure Lengend Snippet: BNT351 shows comparable target affinity to 1-18 and no off-target binding (A) Left: the binding affinity of BNT351 and 1-18 to the stabilized HIV-1 envelope protein trimer (SOSIP BG505.664 ) by SPR (mean and individual values of triplicate measurements). Also see A. Right: binding of BNT351 and 1-18 to SOSIP BG505.664 by ELISA (mean ± standard deviation of triplicate measurements). (B) BNT351’s off-target binding was assessed by Retrogenix Cell Microarray Technology platform. Interactions identified during the library screen with ∼6,500 human proteins are shown. Also, see . Interaction with pepsinogen C (PGC) that appeared to be specific was re-tested by flow cytometry with HEK293 cells transfected with PGC. HEK293 cells transfected with FcγRIIIa and FcεRIg were used as a positive control. Duplicate measurements are shown for flow cytometry.

    Article Snippet: The Retrogenix cell microarray was performed by Charles River Laboratories and included 6,105 full-length human proteins (plasma membrane proteins, secreted or a cell surface-tethered secreted proteins) and 400 human heterodimers.

    Techniques: Binding Assay, Enzyme-linked Immunosorbent Assay, Standard Deviation, Microarray, Flow Cytometry, Transfection, Positive Control