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custom agilent microarray  (Agilent technologies)


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    Agilent technologies custom agilent microarray
    qPCR of sense transcripts regulated by drought stress. The y axis is the normalized relative expression ratio between stressed versus irrigated samples. qPCR reactions were done only for experimental points differentially expressed in <t>microarray</t> experiments. Reactions were done in triplicates and on a third biological replicate. Error bars were calculated as in Rocha et al. ( . ** p = 0.95; *** p = 0.99; * p = 1.00 for control versus drought sample
    Custom Agilent Microarray, supplied by Agilent technologies, 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/custom+agilent+microarray/pmc03369129-281-7-8
    Average 86 stars, based on 1 article reviews
    custom agilent microarray - by Bioz Stars, 2026-10
    86/100 stars

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    1) Product Images from "Identification of sense and antisense transcripts regulated by drought in sugarcane"

    Article Title: Identification of sense and antisense transcripts regulated by drought in sugarcane

    Journal: Plant Molecular Biology

    doi: 10.1007/s11103-012-9922-1

    qPCR of sense transcripts regulated by drought stress. The y axis is the normalized relative expression ratio between stressed versus irrigated samples. qPCR reactions were done only for experimental points differentially expressed in microarray experiments. Reactions were done in triplicates and on a third biological replicate. Error bars were calculated as in Rocha et al. ( . ** p = 0.95; *** p = 0.99; * p = 1.00 for control versus drought sample
    Figure Legend Snippet: qPCR of sense transcripts regulated by drought stress. The y axis is the normalized relative expression ratio between stressed versus irrigated samples. qPCR reactions were done only for experimental points differentially expressed in microarray experiments. Reactions were done in triplicates and on a third biological replicate. Error bars were calculated as in Rocha et al. ( . ** p = 0.95; *** p = 0.99; * p = 1.00 for control versus drought sample

    Techniques Used: Expressing, Microarray

    qPCR of sense and antisense transcripts regulated by drought stress. The y axis is the normalized relative expression ratio between stressed versus irrigated samples. qPCR reactions were done only for experimental points differentially expressed in microarray experiments. Reactions were done in triplicates; on a third biological replicate and using strand specific cDNA as template. Error bars were calculated as in Rocha et al. . * p = 1.00 for control versus drought sample
    Figure Legend Snippet: qPCR of sense and antisense transcripts regulated by drought stress. The y axis is the normalized relative expression ratio between stressed versus irrigated samples. qPCR reactions were done only for experimental points differentially expressed in microarray experiments. Reactions were done in triplicates; on a third biological replicate and using strand specific cDNA as template. Error bars were calculated as in Rocha et al. . * p = 1.00 for control versus drought sample

    Techniques Used: Expressing, Microarray

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    Microarray:

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    Derivative Assay:

    Article Title: Physical Mapping of Bread Wheat Chromosome 5A: An Integrated Approach.
    Article Snippet: .. A custom Agilent microarray, specific for chromosome 5A, was designed using 4722 sequences derived from several resources: (i) ESTs located on chromosome 5A recovered from http://wheat.pw.usda.gov/wEST/; (ii) sequences derived from the wheat GZ v.2 produced in the frame of the consortium and kindly provided by Klaus Mayer (http://wheat-urgi.versailles.inra.fr/Seq-Repository/ Genes-annotations); (iii) restriction fragment length polymorphism (RFLP), SSR, diversity array technology (DArT) markers and exome-based SNPs from the literature; (iv) SSRs and TE-based junction markers developed in this work for 5AS and already genetically mapped in our maps; and (v) the 5AL and 5AS GZ (GZ_1) sequences produced by Vitulo et al. (2011). ..

    Produced:

    Article Title: Physical Mapping of Bread Wheat Chromosome 5A: An Integrated Approach.
    Article Snippet: .. A custom Agilent microarray, specific for chromosome 5A, was designed using 4722 sequences derived from several resources: (i) ESTs located on chromosome 5A recovered from http://wheat.pw.usda.gov/wEST/; (ii) sequences derived from the wheat GZ v.2 produced in the frame of the consortium and kindly provided by Klaus Mayer (http://wheat-urgi.versailles.inra.fr/Seq-Repository/ Genes-annotations); (iii) restriction fragment length polymorphism (RFLP), SSR, diversity array technology (DArT) markers and exome-based SNPs from the literature; (iv) SSRs and TE-based junction markers developed in this work for 5AS and already genetically mapped in our maps; and (v) the 5AL and 5AS GZ (GZ_1) sequences produced by Vitulo et al. (2011). ..

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    Agilent technologies custom agilent microarray
    qPCR of sense transcripts regulated by drought stress. The y axis is the normalized relative expression ratio between stressed versus irrigated samples. qPCR reactions were done only for experimental points differentially expressed in <t>microarray</t> experiments. Reactions were done in triplicates and on a third biological replicate. Error bars were calculated as in Rocha et al. ( . ** p = 0.95; *** p = 0.99; * p = 1.00 for control versus drought sample
    Custom Agilent Microarray, supplied by Agilent technologies, 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/custom+agilent+microarray/pmc03369129-281-7-8
    Average 86 stars, based on 1 article reviews
    custom agilent microarray - by Bioz Stars, 2026-10
    86/100 stars
      Buy from Supplier

    Image Search Results


    qPCR of sense transcripts regulated by drought stress. The y axis is the normalized relative expression ratio between stressed versus irrigated samples. qPCR reactions were done only for experimental points differentially expressed in microarray experiments. Reactions were done in triplicates and on a third biological replicate. Error bars were calculated as in Rocha et al. ( . ** p = 0.95; *** p = 0.99; * p = 1.00 for control versus drought sample

    Journal: Plant Molecular Biology

    Article Title: Identification of sense and antisense transcripts regulated by drought in sugarcane

    doi: 10.1007/s11103-012-9922-1

    Figure Lengend Snippet: qPCR of sense transcripts regulated by drought stress. The y axis is the normalized relative expression ratio between stressed versus irrigated samples. qPCR reactions were done only for experimental points differentially expressed in microarray experiments. Reactions were done in triplicates and on a third biological replicate. Error bars were calculated as in Rocha et al. ( . ** p = 0.95; *** p = 0.99; * p = 1.00 for control versus drought sample

    Article Snippet: Of these, 51 are present on our custom Agilent microarray and 31 genes had the same expression profile in both plataforms.

    Techniques: Expressing, Microarray

    qPCR of sense and antisense transcripts regulated by drought stress. The y axis is the normalized relative expression ratio between stressed versus irrigated samples. qPCR reactions were done only for experimental points differentially expressed in microarray experiments. Reactions were done in triplicates; on a third biological replicate and using strand specific cDNA as template. Error bars were calculated as in Rocha et al. . * p = 1.00 for control versus drought sample

    Journal: Plant Molecular Biology

    Article Title: Identification of sense and antisense transcripts regulated by drought in sugarcane

    doi: 10.1007/s11103-012-9922-1

    Figure Lengend Snippet: qPCR of sense and antisense transcripts regulated by drought stress. The y axis is the normalized relative expression ratio between stressed versus irrigated samples. qPCR reactions were done only for experimental points differentially expressed in microarray experiments. Reactions were done in triplicates; on a third biological replicate and using strand specific cDNA as template. Error bars were calculated as in Rocha et al. . * p = 1.00 for control versus drought sample

    Article Snippet: Of these, 51 are present on our custom Agilent microarray and 31 genes had the same expression profile in both plataforms.

    Techniques: Expressing, Microarray