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arrayworxe scanner  (Applied Precision Inc)

 
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    Applied Precision Inc arrayworxe scanner
    Arrayworxe Scanner, supplied by Applied Precision Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/arrayworx+e+scanner/arrayworxe+scanner/pm26098482-80-6-8
    Average 86 stars, based on 1 article reviews
    arrayworxe scanner - by Bioz Stars, 2026-10
    86/100 stars

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    Related Articles

    Expressing:

    Article Title: Screening for beneficial effects of oral intake of sweet corn by DNA microarray analysis.
    Article Snippet: To identify novel functions of the oral intake of sweet corn, we performed DNA microarray analysis of the livers of sweet corn-fed mice.. Functional annotation clustering 1600 genes with expression levels that were affected (more than 1.5-fold change) by dietary sweet corn indicated that both cell proliferation and programmed cell death were modulated by sweet corn intake.. In the Wnt signaling pathway, which is involved in cell proliferation, the levels of Jun and β-catenin expression were downregulated by dietary sweet corn.

    Article Title: The Oral Intake of Organic Germanium, Ge-132, Elevates α-Tocopherol Levels in the Plas-ma and Modulates Hepatic Gene Expression Profiles to Promote Immune Activation in Mice.
    Article Snippet: The common water-soluble organic germanium compound poly-trans-[(2-carboxyethyl) germasesquioxane] (Ge-132) exhibits activities related to immune responses and antioxidant induction.. In this study, we evaluated the antioxidative effect of dietary Ge-132 in the plasma of mice.. Male ICR mice (seven mice per group) received an AIN-76 diet with 0.05 % Ge-132; three groups received the Ge-132-containing diet for 0, 1 or 4 days.

    Software:

    Article Title: Screening for beneficial effects of oral intake of sweet corn by DNA microarray analysis.
    Article Snippet: To identify novel functions of the oral intake of sweet corn, we performed DNA microarray analysis of the livers of sweet corn-fed mice.. Functional annotation clustering 1600 genes with expression levels that were affected (more than 1.5-fold change) by dietary sweet corn indicated that both cell proliferation and programmed cell death were modulated by sweet corn intake.. In the Wnt signaling pathway, which is involved in cell proliferation, the levels of Jun and β-catenin expression were downregulated by dietary sweet corn.

    Article Title: The Oral Intake of Organic Germanium, Ge-132, Elevates α-Tocopherol Levels in the Plas-ma and Modulates Hepatic Gene Expression Profiles to Promote Immune Activation in Mice.
    Article Snippet: The common water-soluble organic germanium compound poly-trans-[(2-carboxyethyl) germasesquioxane] (Ge-132) exhibits activities related to immune responses and antioxidant induction.. In this study, we evaluated the antioxidative effect of dietary Ge-132 in the plasma of mice.. Male ICR mice (seven mice per group) received an AIN-76 diet with 0.05 % Ge-132; three groups received the Ge-132-containing diet for 0, 1 or 4 days.

    Fluorescence:

    Article Title: Large impact of the apoplast on somatic embryogenesis in Cyclamen persicum offers possibilities for improved developmental control in vitro.
    Article Snippet: .. The slides were scanned at 10 μm resolution with an ArrayWorXe scanner (Applied Precision, Washington, USA) and two-channel images were obtained for subsequent quantification of both Cy3 and Cy5 fluorescence intensities. .. Median pixel intensities of the spots were collected using GenePix Pro v. 6.1.0.2 (Molecular Devices, CA, USA).

    Article Title: Large impact of the apoplast on somatic embryogenesis in Cyclamen persicum offers possibilities for improved developmental control in vitro
    Article Snippet: .. The slides were scanned at 10 μm resolution with an ArrayWorXe scanner (Applied Precision, Washington, USA) and two-channel images were obtained for subsequent quantification of both Cy3 and Cy5 fluorescence intensities. .. Median pixel intensities of the spots were collected using GenePix Pro v. 6.1.0.2 (Molecular Devices, CA, USA).

    In Situ Hybridization:

    Article Title: Ovine fetal necrobacillosis.
    Article Snippet: The association of Fusobacterium necrophorumwith late term abortion in sheep is reported.The bacterium was not culturable, but was identi¢ed in ¢ve cases by £uorescence in-situ hybridization (FISH) with an oligonucleotide probe speci¢cally targeting16S rRNA in F. necrophorum.Gross lesions were found in several tissues.. Histologically, placental lesions were characterizedby locally di¡use in¢ltration of neutrophils, closely associatedwith abundant small Gram-negative and FISH-positive rods, thrombosis and necrosis.. Lesions in the fetal^maternal interface were multifocal and consisted of villous necrosis and suppurative in£ammation.



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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