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human mirna microarray rel12.0 platform  (Agilent technologies)


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    Agilent technologies human mirna microarray rel12.0 platform
    Human Mirna Microarray Rel12.0 Platform, 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/product/human+mirna+microarray+platform/pmc07802940-62-9-10
    Average 90 stars, based on 1 article reviews
    human mirna microarray rel12.0 platform - by Bioz Stars, 2026-10
    90/100 stars

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    other:

    Article Title: Identification of biomarkers and construction of a microRNA‑mRNA regulatory network for clear cell renal cell carcinoma using integrated bioinformatics analysis
    Article Snippet: In https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE16441 download the series matrix file (s) and GPL8659 Agilent human miRNA microarray rel12.0 platform files.

    Article Title: Identification of biomarkers and construction of a microRNA‑mRNA regulatory network for clear cell renal cell carcinoma using integrated bioinformatics analysis
    Article Snippet: All samples were detected by the platform GPL8659 Agilent human miRNA microarray rel12.0.



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    Image Search Results


    Clinicopathological characteristics of TNBC patients in this study.

    Journal: Theranostics

    Article Title: A panel of eight microRNAs is a good predictive parameter for triple-negative breast cancer relapse

    doi: 10.7150/thno.46142

    Figure Lengend Snippet: Clinicopathological characteristics of TNBC patients in this study.

    Article Snippet: The GEOD-40525 dataset was based on an Agilent-019118 Human miRNA Microarray 2.0 platform (n=8).

    Techniques: Preserving, Sequencing, Microarray

    We confirmed the gene expression levels of miRNAs using real-time qPCR. We analyzed the expression of 7 miRNAs (hsa-miR-223, hsa-miR-365 hsa-miR-424, and hsa-miR-451, hsa-miR-144, hsa-miR-500 and hsa-miR-21*) selected from the microarray data by qPCR. The 2 −ΔΔCT method was used to normalize the relative gene expression data in the qPCR assay. U6 snRNA was set as the reference gene. The miRNA expression value in one subject with LTBI was normalized to 1. Statistical analysis was performed using the unpaired t-test. ** P <0.01, * P <0.05, NS: not significant.

    Journal: PLoS ONE

    Article Title: Comparative miRNA Expression Profiles in Individuals with Latent and Active Tuberculosis

    doi: 10.1371/journal.pone.0025832

    Figure Lengend Snippet: We confirmed the gene expression levels of miRNAs using real-time qPCR. We analyzed the expression of 7 miRNAs (hsa-miR-223, hsa-miR-365 hsa-miR-424, and hsa-miR-451, hsa-miR-144, hsa-miR-500 and hsa-miR-21*) selected from the microarray data by qPCR. The 2 −ΔΔCT method was used to normalize the relative gene expression data in the qPCR assay. U6 snRNA was set as the reference gene. The miRNA expression value in one subject with LTBI was normalized to 1. Statistical analysis was performed using the unpaired t-test. ** P <0.01, * P <0.05, NS: not significant.

    Article Snippet: MiRNA microarray assays were performed using the Agilent Human miRNA microarray platform (version 3, Agilent Technologies) at Shanghai Biochip Co., Ltd. (Shanghai, China).

    Techniques: Expressing, Microarray