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gsi scanarray 3000  (Luminomics Inc)

 
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    Luminomics Inc gsi scanarray 3000
    Gsi Scanarray 3000, supplied by Luminomics 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/microarray+scanner+arrayworx+e/gsi+scanarray+3000/us08741630-719-30-35
    Average 90 stars, based on 1 article reviews
    gsi scanarray 3000 - by Bioz Stars, 2026-09
    90/100 stars

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    other:

    Article Title: Microwell array articles and methods of use
    Article Snippet: Exemplary detection instruments useful with the microwell array of the disclosure are well known in the art and include, for example, the GenePix 40008 Array Scanner from Axon Instruments, Inc., GSI Scanarray 3000 from GSI Luminomics, and the like.

    Article Title: Microwell array articles and methods of use
    Article Snippet: Exemplary detection instruments useful with the microwell array of the disclosure are well known in the art and include, for example, the GenePix 40008 Array Scanner from Axon Instruments, Inc., GSI Scanarray 3000 from GSI Luminomics, and the like.

    Microarray:

    Article Title: Methods of detecting targets on an array
    Article Snippet: .. Exemplary detection instruments useful with the composite array of the invention are well known in the art and include, for example, the GenePix 4000B Array Scanner from Axon Instruments, Inc., GSI Scanarray 3000 from GSI Luminomics, arrayWoRx Microarray Scanner from Applied Precision, and the like. ..



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    Anabaena circinalis 131C putative specific sequences with protein matches in The National Center for Biotechnology Information (NCBI) protein database
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    Image Search Results


    a) microfluidic design: the device consists of two PDMS layers: flow (blue) and control (red). The chip is an array of eight rows by 48 columns for 384 unit cells. Each unit cell is composed of: two antibody chambers divided by a reaction chamber (1–2), 4 MITOMI buttons (3), a valve that segregates the unit cells (4), a valve that separates antibody and reaction chambers (5) and a valve for releasing pressure in the antibody chambers (6). b) The PDMS chip is aligned to an epoxy-functionalized slide onto which primary and secondary antibodies were spotted. c) Assay details: schematic of the unit cell and cross section of a button region: i) functionalization of the surface: BSA-biotin is flowed though the chip followed by neutravidin. Next, the buttons are closed and BSA-biotin flowed again to passivate all neutravidin molecules except for those located underneath the MITOMI buttons, ii) the biotinylated primary antibody is allowed to diffuse into the MITOMI detection chamber and is bound by neutravidin immobilizing it in the MITOMI detection regions, iii) the sample is flown through the device and antigens are captured by the surface immobilized antibodies, iv) finally, the fluorescently labeled secondary antibody is allowed to diffuse into the MITOMI area, binds to the antigen if present, and is trapped by MITOMI. The entire device is then quantitated using a DNA microarray scanner.

    Journal: PLoS ONE

    Article Title: A Microfluidic Platform for High-Throughput Multiplexed Protein Quantitation

    doi: 10.1371/journal.pone.0117744

    Figure Lengend Snippet: a) microfluidic design: the device consists of two PDMS layers: flow (blue) and control (red). The chip is an array of eight rows by 48 columns for 384 unit cells. Each unit cell is composed of: two antibody chambers divided by a reaction chamber (1–2), 4 MITOMI buttons (3), a valve that segregates the unit cells (4), a valve that separates antibody and reaction chambers (5) and a valve for releasing pressure in the antibody chambers (6). b) The PDMS chip is aligned to an epoxy-functionalized slide onto which primary and secondary antibodies were spotted. c) Assay details: schematic of the unit cell and cross section of a button region: i) functionalization of the surface: BSA-biotin is flowed though the chip followed by neutravidin. Next, the buttons are closed and BSA-biotin flowed again to passivate all neutravidin molecules except for those located underneath the MITOMI buttons, ii) the biotinylated primary antibody is allowed to diffuse into the MITOMI detection chamber and is bound by neutravidin immobilizing it in the MITOMI detection regions, iii) the sample is flown through the device and antigens are captured by the surface immobilized antibodies, iv) finally, the fluorescently labeled secondary antibody is allowed to diffuse into the MITOMI area, binds to the antigen if present, and is trapped by MITOMI. The entire device is then quantitated using a DNA microarray scanner.

    Article Snippet: The microfluidic device was scanned using a fluorescent microarray scanner (ArrayWorx e-Biochip Reader, Applied Precision, USA).

    Techniques: Control, Labeling, Microarray

    Anabaena circinalis 131C putative specific sequences with protein matches in The National Center for Biotechnology Information (NCBI) protein database

    Journal:

    Article Title: PCR-based positive hybridization to detect genomic diversity associated with bacterial secondary metabolism

    doi: 10.1093/nar/gnh012

    Figure Lengend Snippet: Anabaena circinalis 131C putative specific sequences with protein matches in The National Center for Biotechnology Information (NCBI) protein database

    Article Snippet: Microarray scanning, data acquisition and statistical analyses Clean slides were scanned with the ArrayWorx ‘e’ Microarray Scanner from Applied Precision, Inc. (Issaquah, WA).

    Techniques: Microarray, Hybridization

    Anabaena circinalis 344B putative specific sequences with protein matches (Id: identity; Sim: similarity) in the NCBI protein database

    Journal:

    Article Title: PCR-based positive hybridization to detect genomic diversity associated with bacterial secondary metabolism

    doi: 10.1093/nar/gnh012

    Figure Lengend Snippet: Anabaena circinalis 344B putative specific sequences with protein matches (Id: identity; Sim: similarity) in the NCBI protein database

    Article Snippet: Microarray scanning, data acquisition and statistical analyses Clean slides were scanned with the ArrayWorx ‘e’ Microarray Scanner from Applied Precision, Inc. (Issaquah, WA).

    Techniques: Microarray, Hybridization