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8 × 15 k custom oligo-dna microarray design format  (Agilent technologies)


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    Structured Review

    Agilent technologies 8 × 15 k custom oligo-dna microarray design format
    Agreement between qPCR and <t> microarray </t> data
    8 × 15 K Custom Oligo Dna Microarray Design Format, supplied by Agilent technologies, 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/result/8 × 15 k custom oligo-dna microarray design format/product/Agilent technologies
    Average 90 stars, based on 1 article reviews
    8 × 15 k custom oligo-dna microarray design format - by Bioz Stars, 2026-02
    90/100 stars

    Images

    1) Product Images from "Development and validation of a mixed-tissue oligonucleotide DNA microarray for Atlantic bluefin tuna, Thunnus thynnus (Linnaeus, 1758)"

    Article Title: Development and validation of a mixed-tissue oligonucleotide DNA microarray for Atlantic bluefin tuna, Thunnus thynnus (Linnaeus, 1758)

    Journal: BMC Genomics

    doi: 10.1186/s12864-015-2208-7

    Agreement between qPCR and  microarray  data
    Figure Legend Snippet: Agreement between qPCR and microarray data

    Techniques Used: Microarray

    Least-squares regression fit between microarray and qPCR data. The fit between microarray and qPCR non-normalised (non) and normalised (TEF) Log2FC (Fold Change) is shown in respect to the identity line (dashed) for the selected target genes of T. thynnus
    Figure Legend Snippet: Least-squares regression fit between microarray and qPCR data. The fit between microarray and qPCR non-normalised (non) and normalised (TEF) Log2FC (Fold Change) is shown in respect to the identity line (dashed) for the selected target genes of T. thynnus

    Techniques Used: Microarray

    Combined expression profiles of target genes belonging to six largest T. thynnus tissue clusters. The profiles were derived by combining qPCR and microarray data for specific genes using their respective percentile ranks. Nonparametric Kruskal-Wallis test was used to determine statistical significance of the differences between tissues. Letter codes denote statistical significance at p < 0.05
    Figure Legend Snippet: Combined expression profiles of target genes belonging to six largest T. thynnus tissue clusters. The profiles were derived by combining qPCR and microarray data for specific genes using their respective percentile ranks. Nonparametric Kruskal-Wallis test was used to determine statistical significance of the differences between tissues. Letter codes denote statistical significance at p < 0.05

    Techniques Used: Expressing, Derivative Assay, Microarray



    Similar Products

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    Agilent technologies 8 × 15 k custom oligo-dna microarray design format
    Agreement between qPCR and <t> microarray </t> data
    8 × 15 K Custom Oligo Dna Microarray Design Format, supplied by Agilent technologies, 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/result/8 × 15 k custom oligo-dna microarray design format/product/Agilent technologies
    Average 90 stars, based on 1 article reviews
    8 × 15 k custom oligo-dna microarray design format - by Bioz Stars, 2026-02
    90/100 stars
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    Agreement between qPCR and  microarray  data

    Journal: BMC Genomics

    Article Title: Development and validation of a mixed-tissue oligonucleotide DNA microarray for Atlantic bluefin tuna, Thunnus thynnus (Linnaeus, 1758)

    doi: 10.1186/s12864-015-2208-7

    Figure Lengend Snippet: Agreement between qPCR and microarray data

    Article Snippet: After initial screening, unique probes showing no cross-hybridisation potential were selected to produce an 8 × 15 K Agilent custom oligo-DNA microarray design format (Agilent Design ID = 038391), comprising 15,208 user defined features and 536 Agilent positive and negative controls.

    Techniques: Microarray

    Least-squares regression fit between microarray and qPCR data. The fit between microarray and qPCR non-normalised (non) and normalised (TEF) Log2FC (Fold Change) is shown in respect to the identity line (dashed) for the selected target genes of T. thynnus

    Journal: BMC Genomics

    Article Title: Development and validation of a mixed-tissue oligonucleotide DNA microarray for Atlantic bluefin tuna, Thunnus thynnus (Linnaeus, 1758)

    doi: 10.1186/s12864-015-2208-7

    Figure Lengend Snippet: Least-squares regression fit between microarray and qPCR data. The fit between microarray and qPCR non-normalised (non) and normalised (TEF) Log2FC (Fold Change) is shown in respect to the identity line (dashed) for the selected target genes of T. thynnus

    Article Snippet: After initial screening, unique probes showing no cross-hybridisation potential were selected to produce an 8 × 15 K Agilent custom oligo-DNA microarray design format (Agilent Design ID = 038391), comprising 15,208 user defined features and 536 Agilent positive and negative controls.

    Techniques: Microarray

    Combined expression profiles of target genes belonging to six largest T. thynnus tissue clusters. The profiles were derived by combining qPCR and microarray data for specific genes using their respective percentile ranks. Nonparametric Kruskal-Wallis test was used to determine statistical significance of the differences between tissues. Letter codes denote statistical significance at p < 0.05

    Journal: BMC Genomics

    Article Title: Development and validation of a mixed-tissue oligonucleotide DNA microarray for Atlantic bluefin tuna, Thunnus thynnus (Linnaeus, 1758)

    doi: 10.1186/s12864-015-2208-7

    Figure Lengend Snippet: Combined expression profiles of target genes belonging to six largest T. thynnus tissue clusters. The profiles were derived by combining qPCR and microarray data for specific genes using their respective percentile ranks. Nonparametric Kruskal-Wallis test was used to determine statistical significance of the differences between tissues. Letter codes denote statistical significance at p < 0.05

    Article Snippet: After initial screening, unique probes showing no cross-hybridisation potential were selected to produce an 8 × 15 K Agilent custom oligo-DNA microarray design format (Agilent Design ID = 038391), comprising 15,208 user defined features and 536 Agilent positive and negative controls.

    Techniques: Expressing, Derivative Assay, Microarray