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gene expression gene expression profiling  (fluidigm)


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    fluidigm gene expression gene expression profiling
    Gene Expression Gene Expression Profiling, supplied by fluidigm, used in various techniques. Bioz Stars score: 95/100, based on 716 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/array+gene+expression+profiling/96%2E96+Dynamic+Array+IFC+for+Gene+Expression/us12448458-162-10-16
    Average 95 stars, based on 716 article reviews
    gene expression gene expression profiling - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Expressing:

    Article Title: Integrated drivers of basal and acute immunity in diverse human populations.
    Article Snippet: .. The expression of 96 immune genes was measured using the Fluidigm Fast Gene Expression Analysis Using EvaGreen on the BioMark HD System and 96.96 Dynamic Array integrated fluidic circuits. .. Primers were designed using Fluidigm’s D3 Assay Design Tool.

    Gene Expression:

    Article Title: Integrated drivers of basal and acute immunity in diverse human populations.
    Article Snippet: .. The expression of 96 immune genes was measured using the Fluidigm Fast Gene Expression Analysis Using EvaGreen on the BioMark HD System and 96.96 Dynamic Array integrated fluidic circuits. .. Primers were designed using Fluidigm’s D3 Assay Design Tool.

    Article Title: Regional FDL tendon properties are regulated by biglycan in a collagen VI-independent manner
    Article Snippet: For WT experiments of regional PCM expression through postnatal development ( & S1), polymerase-chain reaction (PCR) was performed (Thermo Taqman Fast Advanced Master Mix) on pre-amplified cDNA with Taqman probes for Col6a(1 – 3), Bgn, and Abl1 (housekeeper). .. For gene expression analysis via Fluidigm PCR array ( , , , S2-S4), preamplified cDNA was loaded into a 96.96 GE Dynamic Array (Fluidigm) at the Molecular Profiling Facility (University of Pennsylvania). .. A full list of Fluidigm target genes and corresponding Taqman assays can be found in the .

    Article Title: Impacts of drought and manure fertilization on soil and radish resistomes
    Article Snippet: .. To determine the relative abundances of ARGs and MGE-linked genes, high-throughput quantitative PCR (HT-qPCR) was performed in the Gene Expression Unit of the Genomics Facility of SGIker (University of the Basque Country, Spain), using the BioMark HD Nanofluidic qPCR System combined with 96.96 Dynamic Arrays Integrated Fluidic Circuits (Fluidigm Corporation). ..

    Article Title: Impacts of drought and manure fertilization on soil and radish resistomes.
    Article Snippet: .. To determine the relative abundances of ARGs and MGE-linked genes, high-throughput quantitative PCR (HT-qPCR) was performed in the Gene Expression Unit of the Genomics Facility of SGIker (University of the Basque Country, Spain), using the BioMark HD Nanofluidic qPCR System combined with 96.96 Dynamic Arrays Integrated Fluidic Circuits (Fluidigm Corporation). ..

    Polymerase Chain Reaction:

    Article Title: Regional FDL tendon properties are regulated by biglycan in a collagen VI-independent manner
    Article Snippet: For WT experiments of regional PCM expression through postnatal development ( & S1), polymerase-chain reaction (PCR) was performed (Thermo Taqman Fast Advanced Master Mix) on pre-amplified cDNA with Taqman probes for Col6a(1 – 3), Bgn, and Abl1 (housekeeper). .. For gene expression analysis via Fluidigm PCR array ( , , , S2-S4), preamplified cDNA was loaded into a 96.96 GE Dynamic Array (Fluidigm) at the Molecular Profiling Facility (University of Pennsylvania). .. A full list of Fluidigm target genes and corresponding Taqman assays can be found in the .

    Article Title: Biomarkers and methods of treating PD-1 and PD-L1 related conditions
    Article Snippet: 96 Taqman primer/probe sets were included in the pre-amplification reaction at a final dilution of 0.2× Taqman assay concentration (Applied Biosystems). .. The thermal cycling conditions were as follows: 1 cycle of 50° C. for 15 min, 1 cycle of 70° C. for 2 min, then 18 cycles of 95° C. for 15 sec and 60° C. for 4 min. Pre-amplified cDNA was diluted 1.94-fold and then amplified using Taqman Universal PCR MasterMix (Applied Biosystems) on the BioMark BMK-M-96.96 platform (Fluidigm) according to the manufacturer's instructions. ..

    Real-time Polymerase Chain Reaction:

    Article Title: Impacts of drought and manure fertilization on soil and radish resistomes
    Article Snippet: .. To determine the relative abundances of ARGs and MGE-linked genes, high-throughput quantitative PCR (HT-qPCR) was performed in the Gene Expression Unit of the Genomics Facility of SGIker (University of the Basque Country, Spain), using the BioMark HD Nanofluidic qPCR System combined with 96.96 Dynamic Arrays Integrated Fluidic Circuits (Fluidigm Corporation). ..

    Article Title: Impacts of drought and manure fertilization on soil and radish resistomes.
    Article Snippet: .. To determine the relative abundances of ARGs and MGE-linked genes, high-throughput quantitative PCR (HT-qPCR) was performed in the Gene Expression Unit of the Genomics Facility of SGIker (University of the Basque Country, Spain), using the BioMark HD Nanofluidic qPCR System combined with 96.96 Dynamic Arrays Integrated Fluidic Circuits (Fluidigm Corporation). ..

    Concentration Assay:

    Article Title: A naturalized gut microbiome interacts with dietary fibers to protect against colonic inflammation.
    Article Snippet: Preamplified samples were cleaned with Exonuclease I (4 U/μL, Thermo Scientific, # EN0582) and diluted 10-fold. .. Analysis was performed using 96.96 Dynamic ArrayTM Integrated Fluidic Circuit (IFC, Standard Biotools Inc., #BMK-M-96.96) with a final template concentration of ~800 ng/μL. ..

    Article Title: A naturalized gut microbiome interacts with dietary fibers to protect against colonic inflammation
    Article Snippet: Preamplified samples were cleaned with Exonuclease I (4 U/μL, Thermo Scientific, # EN0582) and diluted 10-fold. .. Analysis was performed using 96.96 Dynamic ArrayTM Integrated Fluidic Circuit (IFC, Standard Biotools Inc., #BMK-M-96.96) with a final template concentration of ~800 ng/μL. ..

    Amplification:

    Article Title: Biomarkers and methods of treating PD-1 and PD-L1 related conditions
    Article Snippet: 96 Taqman primer/probe sets were included in the pre-amplification reaction at a final dilution of 0.2× Taqman assay concentration (Applied Biosystems). .. The thermal cycling conditions were as follows: 1 cycle of 50° C. for 15 min, 1 cycle of 70° C. for 2 min, then 18 cycles of 95° C. for 15 sec and 60° C. for 4 min. Pre-amplified cDNA was diluted 1.94-fold and then amplified using Taqman Universal PCR MasterMix (Applied Biosystems) on the BioMark BMK-M-96.96 platform (Fluidigm) according to the manufacturer's instructions. ..



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    Image Search Results


    Genes analyzed with the  RT 2 Profiler PCR Array—Human  DNA Damage Signaling Pathway kit (Qiagen, Germantown, MD, USA).

    Journal: Current Issues in Molecular Biology

    Article Title: DNA Double-Strand Break Repair Inhibitors: YU238259, A12B4C3 and DDRI-18 Overcome the Cisplatin Resistance in Human Ovarian Cancer Cells, but Not under Hypoxia Conditions

    doi: 10.3390/cimb45100500

    Figure Lengend Snippet: Genes analyzed with the RT 2 Profiler PCR Array—Human DNA Damage Signaling Pathway kit (Qiagen, Germantown, MD, USA).

    Article Snippet: Expression of genes related to cell response to DNA damage was carried out using Real-time PCR using the RT 2 Profiler PCR Array—Human DNA Damage Signaling Pathway gene expression evaluation kit (Qiagen, Germantown, MD, USA).

    Techniques:

    Cross-talk between CoV-2-infected epithelial cells and immune cells activated MAIT and exacerbated inflammation. (A) Heatmap of immunological profile of Caco-2-ACE2-N cells infected with CoV-2 and PBMC cocultured with CoV-2-infected Caco-2-ACE2-N cells. mRNA fold change of immune genes was profiled by RT2 Profiler PCR Array Gene Expression Analysis. Left panel indicated group of CoV-2-infected Caco-2-ACE2-N cells, shortly named with “Caco-2 ACE2-N”; data were presented with mRNA fold change relative to Mock-treated Caco-2-ACE2-N cells. Right panel indicated group of PBMCs cocultured with CoV-2-infected Caco-2-ACE2-N cells, shortly named with “PBMC”; data were presented with mRNA fold change relative to control PBMCs cocultured with Mock-treated Caco-2-ACE2-N cells. (B) CD69 expression profile on MAIT cells in various coculture groups. “Isotype ctr” indicated isotype antibody staining; “Mock” group indicated MAIT cells cocultured with Mock-treated IECs (Caco-2-ACE-2-N); “CoV-2” group indicated MAIT cells cocultured with CoV-2-infected IECs. (C) Representative flow cytometry dot plot of IFNγ expression in NK and MAIT cells after coculture with either Mock or CoV-2 infected IECs (Caco-2-ACE-2-N). (D) Inflammatory cytokine (IFNγ, GrzB, TNFα) expression in MAIT cells determined by FACS with positive population percentage. “Mock” indicated group of MAIT cells cocultured with Mock-treated IECs; “CoV-2” indicated group of MAIT cells cocultured with CoV-2-infected IECs (E) Depletion of IL18 by adding αIL18 Ab into medium at the beginning of coculture. Cytokine expression in MAIT with depletion of IL18 in coculture or with rIL18 addition alone in PBMC culture medium. All data are represented as mean ± SEM of three replicates. Statistical significance is indicated. (ns, not significant, **p<0.01 ***p<0.001, unpaired t test or One-way ANOVA).

    Journal: Frontiers in Cellular and Infection Microbiology

    Article Title: SARS-CoV-2 infection of intestinal epithelia cells sensed by RIG-I and DHX-15 evokes innate immune response and immune cross-talk

    doi: 10.3389/fcimb.2022.1035711

    Figure Lengend Snippet: Cross-talk between CoV-2-infected epithelial cells and immune cells activated MAIT and exacerbated inflammation. (A) Heatmap of immunological profile of Caco-2-ACE2-N cells infected with CoV-2 and PBMC cocultured with CoV-2-infected Caco-2-ACE2-N cells. mRNA fold change of immune genes was profiled by RT2 Profiler PCR Array Gene Expression Analysis. Left panel indicated group of CoV-2-infected Caco-2-ACE2-N cells, shortly named with “Caco-2 ACE2-N”; data were presented with mRNA fold change relative to Mock-treated Caco-2-ACE2-N cells. Right panel indicated group of PBMCs cocultured with CoV-2-infected Caco-2-ACE2-N cells, shortly named with “PBMC”; data were presented with mRNA fold change relative to control PBMCs cocultured with Mock-treated Caco-2-ACE2-N cells. (B) CD69 expression profile on MAIT cells in various coculture groups. “Isotype ctr” indicated isotype antibody staining; “Mock” group indicated MAIT cells cocultured with Mock-treated IECs (Caco-2-ACE-2-N); “CoV-2” group indicated MAIT cells cocultured with CoV-2-infected IECs. (C) Representative flow cytometry dot plot of IFNγ expression in NK and MAIT cells after coculture with either Mock or CoV-2 infected IECs (Caco-2-ACE-2-N). (D) Inflammatory cytokine (IFNγ, GrzB, TNFα) expression in MAIT cells determined by FACS with positive population percentage. “Mock” indicated group of MAIT cells cocultured with Mock-treated IECs; “CoV-2” indicated group of MAIT cells cocultured with CoV-2-infected IECs (E) Depletion of IL18 by adding αIL18 Ab into medium at the beginning of coculture. Cytokine expression in MAIT with depletion of IL18 in coculture or with rIL18 addition alone in PBMC culture medium. All data are represented as mean ± SEM of three replicates. Statistical significance is indicated. (ns, not significant, **p<0.01 ***p<0.001, unpaired t test or One-way ANOVA).

    Article Snippet: After that, PBMC were harvested for immune genes profiling with customized RT2 Profiler PCR Array Gene Expression Kit (Qiagen).

    Techniques: Infection, Gene Expression, Control, Expressing, Staining, Flow Cytometry

    Quality of human ORF features on GMAP chip . (a) Intensity signals from the GMAP array (X-axis) plotted against signals from the Human Gene 1.0 ST array (Y-axis) following amplification of human ORFeome v5.1 pools and hybridization of the resulting probe to each of these arrays. Common features between the two arrays were used to calculate the Pearson correlation coefficient. (b) Distribution of signal intensities from replicate GMAP or Human 1.0 ST arrays as described in (a) for shared features. Hybridization behaviour for the huORF features compared to the (c) huGene features or the (d) 22-mer hairpin features for corresponding genes.

    Journal: BMC Genomics

    Article Title: A comprehensive platform for highly multiplexed mammalian functional genetic screens

    doi: 10.1186/1471-2164-12-213

    Figure Lengend Snippet: Quality of human ORF features on GMAP chip . (a) Intensity signals from the GMAP array (X-axis) plotted against signals from the Human Gene 1.0 ST array (Y-axis) following amplification of human ORFeome v5.1 pools and hybridization of the resulting probe to each of these arrays. Common features between the two arrays were used to calculate the Pearson correlation coefficient. (b) Distribution of signal intensities from replicate GMAP or Human 1.0 ST arrays as described in (a) for shared features. Hybridization behaviour for the huORF features compared to the (c) huGene features or the (d) 22-mer hairpin features for corresponding genes.

    Article Snippet: For comparative purposes, we also included up to three additional features found on the human expression profiling Affymetrix Gene 1.0 ST array for 18,088 of these sequences.

    Techniques: Amplification, Hybridization