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arrayworx auto e scanner  (Applied Precision Inc)

 
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    Applied Precision Inc arrayworx auto e scanner
    Arrayworx Auto E Scanner, supplied by Applied Precision 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/arrayworx+e+scanner/arrayworx+auto+scanner/pmc03359745-96-5-9
    Average 90 stars, based on 1 article reviews
    arrayworx auto e scanner - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Software:

    Article Title: Development of a DNA microarray for detection of expressed equine classical MHC class I sequences in a defined population.
    Article Snippet: .. Arrays were imaged using an arrayWoRx Autoe scanner (Applied Precision, Issaquah, WA, USA), and the images were processed with softWoRx Tracker software (Applied Precision). .. The threshold for positive detection was determined using a receiver operator characteristic (NCSS 2004 Statistical software) curve generated from the binary classification of a core set of probes.

    Article Title: Development of a DNA microarray for detection of expressed equine classical MHC class I sequences in a defined population
    Article Snippet: .. Arrays were imaged using an arrayWoRx Auto e scanner (Applied Precision, Issaquah, WA), and the images were processed with softWoRx Tracker software (Applied Percision). .. The threshold for positive detection was determined using a receiver operator characteristic (ROC; NCSS 2004 Statistical software) curve generated from the binary classification of a core set of probes.

    Article Title: miRNA expression profiles in head and neck squamous cell carcinoma and adjacent normal tissue
    Article Snippet: .. Data Analysis The dried arrays were scanned using the ArrayWorx Auto e scanner (Applied Precision, Issaquah, WA) and the fluorescence quantified using ArrayVision software (Imaging Research, St. Catherines, Ontario, Canada). ..

    Article Title: miRNA expression profiles in head and neck squamous cell carcinoma and adjacent normal tissue
    Article Snippet: .. The dried arrays were scanned using the ArrayWorx Auto e scanner (Applied Precision, Issaquah, WA) and the fluorescence quantified using ArrayVision software (Imaging Research, St. Catherines, Ontario, Canada). ..

    other:

    Article Title: Development and validation of a resistance and virulence gene microarray targeting Escherichia coli and Salmonella enterica
    Article Snippet: Individual spot-intensities were annotated using softWoRx Tracker software (Applied Precision) and exported to an Excel (Microsoft, Redmond, WA) spreadsheet for analysis.

    Fluorescence:

    Article Title: miRNA expression profiles in head and neck squamous cell carcinoma and adjacent normal tissue
    Article Snippet: .. Data Analysis The dried arrays were scanned using the ArrayWorx Auto e scanner (Applied Precision, Issaquah, WA) and the fluorescence quantified using ArrayVision software (Imaging Research, St. Catherines, Ontario, Canada). ..

    Article Title: miRNA expression profiles in head and neck squamous cell carcinoma and adjacent normal tissue
    Article Snippet: .. The dried arrays were scanned using the ArrayWorx Auto e scanner (Applied Precision, Issaquah, WA) and the fluorescence quantified using ArrayVision software (Imaging Research, St. Catherines, Ontario, Canada). ..

    Imaging:

    Article Title: miRNA expression profiles in head and neck squamous cell carcinoma and adjacent normal tissue
    Article Snippet: .. Data Analysis The dried arrays were scanned using the ArrayWorx Auto e scanner (Applied Precision, Issaquah, WA) and the fluorescence quantified using ArrayVision software (Imaging Research, St. Catherines, Ontario, Canada). ..

    Article Title: miRNA expression profiles in head and neck squamous cell carcinoma and adjacent normal tissue
    Article Snippet: .. The dried arrays were scanned using the ArrayWorx Auto e scanner (Applied Precision, Issaquah, WA) and the fluorescence quantified using ArrayVision software (Imaging Research, St. Catherines, Ontario, Canada). ..



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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