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two-color human ge 4x44k microarrays platform  (Agilent technologies)


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    Agilent technologies two-color human ge 4x44k microarrays platform
    Two Color Human Ge 4x44k Microarrays 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/two-color+microarray+platform/pmc04100821-75-1-7
    Average 90 stars, based on 1 article reviews
    two-color human ge 4x44k microarrays platform - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Rice peroxygenase catalyzes lipoxygenase-dependent regiospecific epoxidation of lipid peroxides in the response to abiotic stressors.
    Article Snippet: The peroxygenase pathway plays pivotal roles in plant responses to oxidative stress and other environmental stressors.. Analysis of a network of co-expressed stress-regulated rice genes demonstrated that expression of OsPXG9 is negatively correlated with expression of genes involved in jasmonic acid biosynthesis.. DNA sequence analysis and structure/function studies reveal that OsPXG9 is a caleosin-like peroxygenase with amphipathic α-helices that localizes to lipid droplets in rice cells.

    Article Title: Mucins 3A and 3B Are Expressed in the Epithelium of Human Large Airway.
    Article Snippet: Equal amounts of Cy3-labeled target were hybridized to Agilent human whole-genome 4x44K Ink-jet arrays containing a total of 41,000 probes corresponding to 19,596 entrez genes.

    Article Title: A prognostic and immunotherapeutic predictive model based on the cell-originated characterization of tumor microenvironment in lung adenocarcinoma
    Article Snippet: Platform , Illu.HiSeq V2 , Agilent. 4x44K , Affy.Plus 2 , Affy.Plus 2 , Illu.WG-6 V3 , Affy.Plus 2 , Affy.Plus 2 , Affy.U133A , Affy. 2.0 , Affymetrix HuEx-1_0-st , Illu.HiSeq 2500 , Illu.HiSeq 2500 , , .

    Article Title: Role of ABCB1 and ABCB4 in renal and biliary excretion of perfluorooctanoic acid in mice
    Article Snippet: Cyanine-labeled cDNA was synthesized from the total RNA samples and hybridized to oligo DNA microarray slides (Whole Mouse Genome 4x44k; Agilent Technologies Japan).

    Microarray:

    Article Title: Prognostic marker for myeloproliferative neoplasms
    Article Snippet: .. For microarray analysis, RNA was hybridized on Agilent 4X44K arrays following manufacturer's procedures. ..

    Article Title: Mesothelioma-associated fibroblasts enhance proliferation and migration of pleural mesothelioma cells via c-Met/PI3K and WNT signaling but do not protect against cisplatin.
    Article Snippet: Whole genome gene expression microarrays Total RNA of Meso-CAFs and CAF-3 was extracted from primary cell cultures of about 80% confluence with RNeasy Mini Kit (Qiagen Sciences, Germantown, MD, USA) according to the respective protocol of the manufacturer. .. Whole-genome gene expression analysis was carried out as described previously by Pirker et al. [11] and Mathieu et al. [13] using 4x44K whole genome oligonucleotidebased gene expression microarrays (Agilent, Santa Clara, CA, USA) and a G2505B Micro Array Scanner (Agilent, Santa Clara, CA, USA). ..

    Purification:

    Article Title: A systems genomics and genetics approach to identify the genetic regulatory network for lignin content in Brassica napus seeds
    Article Snippet: cRNAs were amplified from total RNA samples (2 μg) and labelled with either cy3 or cy5 using the Quick Amp labelling kit, Two Colour (Agilent, Catalogue: 5190-0444) according to the manufacturer’s instructions, followed by purification with the Qiagen RNeasy Mini Kit (Qiagen, Catalogue 74104) and quantification with a NanoDrop ND-1000. .. Purified cRNAs (2 μg) were fragmented and hybridized to the Agilent 4x44K Brassica arrays ( ) for 17 h at 65°C with a rotation of 10 rpm according to the manufacturer’s protocol. .. Arrays were washed with the Agilent Gene Expression Washing buffers according to the manufacturer’s protocol and scanned with GenePix 4000B as described by .

    Gene Expression:

    Article Title: Mesothelioma-associated fibroblasts enhance proliferation and migration of pleural mesothelioma cells via c-Met/PI3K and WNT signaling but do not protect against cisplatin.
    Article Snippet: Whole genome gene expression microarrays Total RNA of Meso-CAFs and CAF-3 was extracted from primary cell cultures of about 80% confluence with RNeasy Mini Kit (Qiagen Sciences, Germantown, MD, USA) according to the respective protocol of the manufacturer. .. Whole-genome gene expression analysis was carried out as described previously by Pirker et al. [11] and Mathieu et al. [13] using 4x44K whole genome oligonucleotidebased gene expression microarrays (Agilent, Santa Clara, CA, USA) and a G2505B Micro Array Scanner (Agilent, Santa Clara, CA, USA). ..



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    Three groups of three mice received binocular HOKS for 24 h in the P→A direction with respect to the right eye. Total RNA was extracted from the left and right flocculi of each mouse and combined for each group. The RNA from each group was analyzed on a miRNA <t>microarray,</t> and subsequently combined for analysis. A. Each data point in the Volcano plot represents four variables: 1) The fold change for each miRNA is represented on abscissa (right floc./left floc), 2) Statistical probability transcription difference (p-value) of a miRNA between the left and right flocculi is represented on left ordinate, 3) Average copy number (color coded) is represented on right ordinate and 4) Frequency of occurrence a miRNA relative to all other sampled miRNAs is represented as data point diameter. B. Twelve miRNAs were screened using three criteria: 1) A fold change >2, 2) A p-value <0.005, and 3) An average copy number >256. Error bars indicate standard error of the mean. Histogram color indicates copy number according to the right ordinate in A.
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    Image Search Results


    The scatter-plots show RT-PCR quantification cycle (C q ) values and log 2 -transformed microarray signal values for microRNAs let-7e , miR-22 , miR-30a-5p , miR-185 , miR-210 , and miR-423-5p (n = 11). Pearson correlation coefficients (r) and their 95% confidence intervals and associated P values, and best fitting (least squares) lines are also shown.

    Journal: PLoS ONE

    Article Title: MicroRNA Expression Profiles of Whole Blood in Lung Adenocarcinoma

    doi: 10.1371/journal.pone.0046045

    Figure Lengend Snippet: The scatter-plots show RT-PCR quantification cycle (C q ) values and log 2 -transformed microarray signal values for microRNAs let-7e , miR-22 , miR-30a-5p , miR-185 , miR-210 , and miR-423-5p (n = 11). Pearson correlation coefficients (r) and their 95% confidence intervals and associated P values, and best fitting (least squares) lines are also shown.

    Article Snippet: A two-color, oligonucleotide microarray platform from Exiqon® was used to quantify levels of 1282 human microRNAs and 23 human non-microRNAs of <200 nucleotides in the RNA isolated from whole blood specimens.

    Techniques: Reverse Transcription Polymerase Chain Reaction, Transformation Assay, Microarray

    A . Unsupervised clustering of the 45 samples of this study by log 2 -transformed microarray signal values of all 395 expressed microRNAs. The numbers indicate identities of the 45 subjects, with cases (n = 22) and controls (n = 23) shown in black and grey, respectively. The sample tree with optimized leaf-ordering is drawn using Pearson correlation for distance metric and average linkage for cluster-to-cluster distance, and the scale for it represents node-heights. B . Supervised clustering of microRNAs by their log 2 -transformed microarray signal values. The heat-map, with the pseudo-color scale underneath, shows log 2 -transformed microarray signal values of the 43 microRNAs whose expression is altered >25% in either direction in the cases compared to the controls. The gene tree is drawn as in A .

    Journal: PLoS ONE

    Article Title: MicroRNA Expression Profiles of Whole Blood in Lung Adenocarcinoma

    doi: 10.1371/journal.pone.0046045

    Figure Lengend Snippet: A . Unsupervised clustering of the 45 samples of this study by log 2 -transformed microarray signal values of all 395 expressed microRNAs. The numbers indicate identities of the 45 subjects, with cases (n = 22) and controls (n = 23) shown in black and grey, respectively. The sample tree with optimized leaf-ordering is drawn using Pearson correlation for distance metric and average linkage for cluster-to-cluster distance, and the scale for it represents node-heights. B . Supervised clustering of microRNAs by their log 2 -transformed microarray signal values. The heat-map, with the pseudo-color scale underneath, shows log 2 -transformed microarray signal values of the 43 microRNAs whose expression is altered >25% in either direction in the cases compared to the controls. The gene tree is drawn as in A .

    Article Snippet: A two-color, oligonucleotide microarray platform from Exiqon® was used to quantify levels of 1282 human microRNAs and 23 human non-microRNAs of <200 nucleotides in the RNA isolated from whole blood specimens.

    Techniques: Transformation Assay, Microarray, Expressing

    Dot-plots with medians and inter-quartile ranges of log 2 -transformed microarray signal values for the 22 cases ( black ) and 23 controls ( grey ) are shown for the four microRNAs that are present in a majority of the classifiers generated in internal cross-validation analyses using the linear support vector machines and top-scoring pairs classification methods.

    Journal: PLoS ONE

    Article Title: MicroRNA Expression Profiles of Whole Blood in Lung Adenocarcinoma

    doi: 10.1371/journal.pone.0046045

    Figure Lengend Snippet: Dot-plots with medians and inter-quartile ranges of log 2 -transformed microarray signal values for the 22 cases ( black ) and 23 controls ( grey ) are shown for the four microRNAs that are present in a majority of the classifiers generated in internal cross-validation analyses using the linear support vector machines and top-scoring pairs classification methods.

    Article Snippet: A two-color, oligonucleotide microarray platform from Exiqon® was used to quantify levels of 1282 human microRNAs and 23 human non-microRNAs of <200 nucleotides in the RNA isolated from whole blood specimens.

    Techniques: Transformation Assay, Microarray, Generated, Plasmid Preparation

    A . Receiver operating characteristic curves, the areas under curve ( AUC ) for age, and the line of identity, x = y , with an AUC of 0.5, are shown. B . Correlation with microRNA expression. Values for the clinical variables were correlated with microarray signal values for the 395 expressed microRNAs (n = 45 for age; n = 39 for others). The curves depict frequency histograms of Pearson correlation coefficients ( r ) with a bin of 0.025. Curves were smoothened using four neighbors for averaging and a zero order polynomial. Correlations are also shown for the random variable resampled WBC count for which values were generated by resampling the WBC count data.

    Journal: PLoS ONE

    Article Title: MicroRNA Expression Profiles of Whole Blood in Lung Adenocarcinoma

    doi: 10.1371/journal.pone.0046045

    Figure Lengend Snippet: A . Receiver operating characteristic curves, the areas under curve ( AUC ) for age, and the line of identity, x = y , with an AUC of 0.5, are shown. B . Correlation with microRNA expression. Values for the clinical variables were correlated with microarray signal values for the 395 expressed microRNAs (n = 45 for age; n = 39 for others). The curves depict frequency histograms of Pearson correlation coefficients ( r ) with a bin of 0.025. Curves were smoothened using four neighbors for averaging and a zero order polynomial. Correlations are also shown for the random variable resampled WBC count for which values were generated by resampling the WBC count data.

    Article Snippet: A two-color, oligonucleotide microarray platform from Exiqon® was used to quantify levels of 1282 human microRNAs and 23 human non-microRNAs of <200 nucleotides in the RNA isolated from whole blood specimens.

    Techniques: Expressing, Microarray, Generated

    Eight fragments of Stylophora pistillata were incubated in calcium seawater (SW) concentrations of seawater plus 100 mg/L calcium (SW + 100) and plus 200 mg/L calcium (SW + 200) during daytime (11:00) and during night-time (23:00). In each sampling time, four replicates were analyzed for calcification rates and four replicates from SW and SW+100 treatments, for microarray analysis.

    Journal: PeerJ

    Article Title: Identifying genes and regulatory pathways associated with the scleractinian coral calcification process

    doi: 10.7717/peerj.3590

    Figure Lengend Snippet: Eight fragments of Stylophora pistillata were incubated in calcium seawater (SW) concentrations of seawater plus 100 mg/L calcium (SW + 100) and plus 200 mg/L calcium (SW + 200) during daytime (11:00) and during night-time (23:00). In each sampling time, four replicates were analyzed for calcification rates and four replicates from SW and SW+100 treatments, for microarray analysis.

    Article Snippet: Total RNA was labeled and hybridized against custom S. pistillata microarray; an Agilent two-color gene expression microarray platform with 8 × 15 K probe per slide; microarray samples included four SW+100 and four SW (control) samples for each time point (11:00 and 23:00).

    Techniques: Incubation, Sampling, Microarray

    Three groups of three mice received binocular HOKS for 24 h in the P→A direction with respect to the right eye. Total RNA was extracted from the left and right flocculi of each mouse and combined for each group. The RNA from each group was analyzed on a miRNA microarray, and subsequently combined for analysis. A. Each data point in the Volcano plot represents four variables: 1) The fold change for each miRNA is represented on abscissa (right floc./left floc), 2) Statistical probability transcription difference (p-value) of a miRNA between the left and right flocculi is represented on left ordinate, 3) Average copy number (color coded) is represented on right ordinate and 4) Frequency of occurrence a miRNA relative to all other sampled miRNAs is represented as data point diameter. B. Twelve miRNAs were screened using three criteria: 1) A fold change >2, 2) A p-value <0.005, and 3) An average copy number >256. Error bars indicate standard error of the mean. Histogram color indicates copy number according to the right ordinate in A.

    Journal:

    Article Title: CLIMBING FIBERS INDUCE microRNA TRANSCRIPTION IN CEREBELLAR PURKINJE CELLS

    doi: 10.1016/j.neuroscience.2010.09.039

    Figure Lengend Snippet: Three groups of three mice received binocular HOKS for 24 h in the P→A direction with respect to the right eye. Total RNA was extracted from the left and right flocculi of each mouse and combined for each group. The RNA from each group was analyzed on a miRNA microarray, and subsequently combined for analysis. A. Each data point in the Volcano plot represents four variables: 1) The fold change for each miRNA is represented on abscissa (right floc./left floc), 2) Statistical probability transcription difference (p-value) of a miRNA between the left and right flocculi is represented on left ordinate, 3) Average copy number (color coded) is represented on right ordinate and 4) Frequency of occurrence a miRNA relative to all other sampled miRNAs is represented as data point diameter. B. Twelve miRNAs were screened using three criteria: 1) A fold change >2, 2) A p-value <0.005, and 3) An average copy number >256. Error bars indicate standard error of the mean. Histogram color indicates copy number according to the right ordinate in A.

    Article Snippet: The spindle shaped mouse flocculus is ~1.1 mm in axial length, ~400 μm at its peak diameter and weighs ~400 μg. miRNA microarray analysis miRNA expression profiling of mouse flocculus was performed using a two-color microarray platform (Asuragen Technical Services, Austin, TX).

    Techniques: Microarray