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high dna microarray scanner g2505c  (Agilent technologies)


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    Agilent technologies high dna microarray scanner g2505c
    High Dna Microarray Scanner G2505c, 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/high+dna+microarray+scanner+g2505c/pmc10500703-586-17-16?v=Agilent+technologies
    Average 90 stars, based on 1 article reviews
    high dna microarray scanner g2505c - by Bioz Stars, 2026-07
    90/100 stars

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    Top 20 aberrantly expressed lncRNAs in  microarray  analysis

    Journal: Translational Andrology and Urology

    Article Title: A comprehensive evaluation of differentially expressed mRNAs and lncRNAs in cystitis glandularis with gene ontology, KEGG pathway, and ceRNA network analysis

    doi: 10.21037/tau.2020.03.01

    Figure Lengend Snippet: Top 20 aberrantly expressed lncRNAs in microarray analysis

    Article Snippet: The hybridized arrays were washed, fixed and scanned using an Agilent Technologies G2505C SureScan High-Resolution DNA Microarray Scanner (Agilent Technologies, Santa Clara, CA, USA).

    Techniques: Microarray

    Top 20 aberrantly expressed mRNAs in  microarray  analysis

    Journal: Translational Andrology and Urology

    Article Title: A comprehensive evaluation of differentially expressed mRNAs and lncRNAs in cystitis glandularis with gene ontology, KEGG pathway, and ceRNA network analysis

    doi: 10.21037/tau.2020.03.01

    Figure Lengend Snippet: Top 20 aberrantly expressed mRNAs in microarray analysis

    Article Snippet: The hybridized arrays were washed, fixed and scanned using an Agilent Technologies G2505C SureScan High-Resolution DNA Microarray Scanner (Agilent Technologies, Santa Clara, CA, USA).

    Techniques: Microarray

    The expression microarray profiles of differentially lncRNAs (DE-lncRNAs) and coding RNAs (DE-mRNAs) in samples from three pairs of CG tissues and normal tissue. (A) DE-lncRNAs and DE-mRNAs are identified on a Volcano plot. Expression was plotted as P values of significance difference of expression (Y-axis) versus fold-difference in expression (X-axis). Horizontal green line marks a P value of 0.05. Vertical green lines mark a 2-fold increased or decreased expression in comparison to normal bladder mucosa; (B) heat map showing the expression profiles of lncRNAs and mRNAs. There were 436 differentially expressed lncRNAs and 809 differentially expressed mRNAs identified. The maps are based on the expression values of all expressed lncRNAs and mRNAs detected by microarray analysis and correspond to normalized expression values of significantly changed lncRNAs and mRNAs with 2-FCs in expression relative to normal tissue (P<0.05). Results from each tissue sample are presented in columns (normal 1–3 and CG 1–3). Red and green lines indicate high and low expression, respectively, of different RNAs. The intensity of expression is shown in the Color Key and Histogram. CG, cystitis glandularis; FC, fold change; DE, differential expression; lncRNA, long non-coding RNA; mRNA, messenger RNA.

    Journal: Translational Andrology and Urology

    Article Title: A comprehensive evaluation of differentially expressed mRNAs and lncRNAs in cystitis glandularis with gene ontology, KEGG pathway, and ceRNA network analysis

    doi: 10.21037/tau.2020.03.01

    Figure Lengend Snippet: The expression microarray profiles of differentially lncRNAs (DE-lncRNAs) and coding RNAs (DE-mRNAs) in samples from three pairs of CG tissues and normal tissue. (A) DE-lncRNAs and DE-mRNAs are identified on a Volcano plot. Expression was plotted as P values of significance difference of expression (Y-axis) versus fold-difference in expression (X-axis). Horizontal green line marks a P value of 0.05. Vertical green lines mark a 2-fold increased or decreased expression in comparison to normal bladder mucosa; (B) heat map showing the expression profiles of lncRNAs and mRNAs. There were 436 differentially expressed lncRNAs and 809 differentially expressed mRNAs identified. The maps are based on the expression values of all expressed lncRNAs and mRNAs detected by microarray analysis and correspond to normalized expression values of significantly changed lncRNAs and mRNAs with 2-FCs in expression relative to normal tissue (P<0.05). Results from each tissue sample are presented in columns (normal 1–3 and CG 1–3). Red and green lines indicate high and low expression, respectively, of different RNAs. The intensity of expression is shown in the Color Key and Histogram. CG, cystitis glandularis; FC, fold change; DE, differential expression; lncRNA, long non-coding RNA; mRNA, messenger RNA.

    Article Snippet: The hybridized arrays were washed, fixed and scanned using an Agilent Technologies G2505C SureScan High-Resolution DNA Microarray Scanner (Agilent Technologies, Santa Clara, CA, USA).

    Techniques: Expressing, Microarray, Comparison

    CNC network analysis. (A) qRT-PCR was used to validate the up-regulated DE of four mRNAs found on microarray analysis; (B) the CNC network included sequences with a Pearson’s correlation coefficient ≥0.7. Green nodes represent dysregulated lncRNAs; yellow nodes represent four mRNAs: SMAD3, ORC1, CCNA2 and CCNB2; solid lines between lncRNAs and mRNAs indicate a positive correlation; dotted lines between lncRNAs and mRNAs indicate a negative correlation. The network consists of four mRNAs and 37 related genes; (C) qRT-PCR was used to validate the up-regulated DE of four lnRNAs found in the microarray analysis. The Y-axis indicates the FC (log2 transformed) computed from the qPCR and microarray data. Gene expression is normalized to β-actin and presented as mean ± SD. All the mRNAs and lncRNAs were up-regulated in the CG tissues (*, P<0.05). CNC, coding-non-coding co-expression; FC, fold change; qRT-PCR, quantitative real-time PCR; DE, differential expression; lncRNA, long non-coding RNA; mRNA, messenger RNA; CG, cystitis glandularis; N, normal.

    Journal: Translational Andrology and Urology

    Article Title: A comprehensive evaluation of differentially expressed mRNAs and lncRNAs in cystitis glandularis with gene ontology, KEGG pathway, and ceRNA network analysis

    doi: 10.21037/tau.2020.03.01

    Figure Lengend Snippet: CNC network analysis. (A) qRT-PCR was used to validate the up-regulated DE of four mRNAs found on microarray analysis; (B) the CNC network included sequences with a Pearson’s correlation coefficient ≥0.7. Green nodes represent dysregulated lncRNAs; yellow nodes represent four mRNAs: SMAD3, ORC1, CCNA2 and CCNB2; solid lines between lncRNAs and mRNAs indicate a positive correlation; dotted lines between lncRNAs and mRNAs indicate a negative correlation. The network consists of four mRNAs and 37 related genes; (C) qRT-PCR was used to validate the up-regulated DE of four lnRNAs found in the microarray analysis. The Y-axis indicates the FC (log2 transformed) computed from the qPCR and microarray data. Gene expression is normalized to β-actin and presented as mean ± SD. All the mRNAs and lncRNAs were up-regulated in the CG tissues (*, P<0.05). CNC, coding-non-coding co-expression; FC, fold change; qRT-PCR, quantitative real-time PCR; DE, differential expression; lncRNA, long non-coding RNA; mRNA, messenger RNA; CG, cystitis glandularis; N, normal.

    Article Snippet: The hybridized arrays were washed, fixed and scanned using an Agilent Technologies G2505C SureScan High-Resolution DNA Microarray Scanner (Agilent Technologies, Santa Clara, CA, USA).

    Techniques: Quantitative RT-PCR, Microarray, Transformation Assay, Expressing, Real-time Polymerase Chain Reaction