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Fisher Scientific microarray gene analyses
Microarray Gene Analyses, supplied by Fisher Scientific, 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/gene+microarray+analyses/microarray+analysis/10__1096_slash_fj__201700289r-115-12-21
Average 90 stars, based on 1 article reviews
microarray gene analyses - by Bioz Stars, 2026-11
90/100 stars

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Expressing:

Article Title: IL‐17A deficiency mitigates bleomycin‐induced complement activation during lung fibrosis
Article Snippet: .. IL-17A activates C9 by modulating the mRNA and protein expression of the C9 components in vitro Microarray gene analyses (Affymetrix; Thermo Fisher Scientific) of normal primary human SAECs exposed to IL-17A for 24 h revealed a;5- and;1.75-fold induction of C3 and C9 factor B mRNA, respectively (Table 2; N = 5 donor lungs), and ;1.4-fold induction of GRK5. ..

In Vitro:

Article Title: IL‐17A deficiency mitigates bleomycin‐induced complement activation during lung fibrosis
Article Snippet: .. IL-17A activates C9 by modulating the mRNA and protein expression of the C9 components in vitro Microarray gene analyses (Affymetrix; Thermo Fisher Scientific) of normal primary human SAECs exposed to IL-17A for 24 h revealed a;5- and;1.75-fold induction of C3 and C9 factor B mRNA, respectively (Table 2; N = 5 donor lungs), and ;1.4-fold induction of GRK5. ..

Microarray:

Article Title: IL‐17A deficiency mitigates bleomycin‐induced complement activation during lung fibrosis
Article Snippet: .. IL-17A activates C9 by modulating the mRNA and protein expression of the C9 components in vitro Microarray gene analyses (Affymetrix; Thermo Fisher Scientific) of normal primary human SAECs exposed to IL-17A for 24 h revealed a;5- and;1.75-fold induction of C3 and C9 factor B mRNA, respectively (Table 2; N = 5 donor lungs), and ;1.4-fold induction of GRK5. ..

Article Title: Circulating tumor cells reveal early predictors of disease progression in patients with stage III NSCLC undergoing chemoradiation and immunotherapy.
Article Snippet: Affymetrix Clariom S PICO microarray processing After thawing gently on ice, 11mL of the RNA samples were plated into a sterile barcoded PCR plate supplied by Thermo Fisher. .. The samples were then shipped to Fisher scientific for microarray services by their lab. ..

Article Title: IL-17A deficiency mitigates bleomycin-induced complement activation during lung fibrosis
Article Snippet: .. Baseline and pulmonary function characteristics of IPF patients Microarray analysis SAECs were treated with IL-17A (100 ng/ml) for 24 h. RNA was isolated, and cDNA was subjected to microarray analysis (Affymetrix; Thermo Fisher Scientific, Waltham, MA, USA) by the Microarray Core (University of Texas Southwest Medical Center, Dallas, TX, USA). .. Real-time PCR Real-time PCR was performed on cDNA from cell lysates, as reported in several publications ( 3 , 13 , 26 , 30 , 31 ), by using gene-specific Taqman assays (Thermo Fisher Scientific).

Article Title: An integrative proteomics method identifies a regulator of translation during stem cell maintenance and differentiation
Article Snippet: .. The microarray analysis was performed according to the manufacturer’s instructions (Termo Fischer Scientific UserGuide P/N 703174). .. Procedures for cDNA synthesis, target DNA fragmentation, and labelling were carried out according to the GeneChip WT PLUS Reagent Kit (Applied Biosystems) using 500 ng of total RNA as the starting material.

Article Title: Response of peripheral blood basophils in subjects with chronic spontaneous urticaria during treatment with omalizumab.
Article Snippet: Background: Treatment of patients with asthma or food allergy with omalizumab results in several consistent changes in circulating basophils.. The multiple basophil phenotypes observed in patients with chronic spontaneous urticaria (CSU) present some unique attributes that may not respond in a similar fashion to patients with asthma or food allergy.. As part of a clinical study on the therapeutic outcomes of omalizumab treatment in CSU, the basophil compartment was examined for changes in characteristics predicted by prior studies.

Isolation:

Article Title: IL-17A deficiency mitigates bleomycin-induced complement activation during lung fibrosis
Article Snippet: .. Baseline and pulmonary function characteristics of IPF patients Microarray analysis SAECs were treated with IL-17A (100 ng/ml) for 24 h. RNA was isolated, and cDNA was subjected to microarray analysis (Affymetrix; Thermo Fisher Scientific, Waltham, MA, USA) by the Microarray Core (University of Texas Southwest Medical Center, Dallas, TX, USA). .. Real-time PCR Real-time PCR was performed on cDNA from cell lysates, as reported in several publications ( 3 , 13 , 26 , 30 , 31 ), by using gene-specific Taqman assays (Thermo Fisher Scientific).

Article Title: Response of peripheral blood basophils in subjects with chronic spontaneous urticaria during treatment with omalizumab.
Article Snippet: Background: Treatment of patients with asthma or food allergy with omalizumab results in several consistent changes in circulating basophils.. The multiple basophil phenotypes observed in patients with chronic spontaneous urticaria (CSU) present some unique attributes that may not respond in a similar fashion to patients with asthma or food allergy.. As part of a clinical study on the therapeutic outcomes of omalizumab treatment in CSU, the basophil compartment was examined for changes in characteristics predicted by prior studies.



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Image Search Results


A hierarchical heatmap comparing global mRNA levels to RISC-IP mRNA levels in U-87 astrocytoma and primary astrocytes. MRNAs included in the heatmap had a fold change >1.4 and were significantly expressed (p<0.01).

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: A hierarchical heatmap comparing global mRNA levels to RISC-IP mRNA levels in U-87 astrocytoma and primary astrocytes. MRNAs included in the heatmap had a fold change >1.4 and were significantly expressed (p<0.01).

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques:

RISC-immunoprecipitated  mRNA  compared to global cellular  mRNA  in U-87 astrocytoma cells and primary  astrocytes  with a fold change > ±1.8 (p <0.01).

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: RISC-immunoprecipitated mRNA compared to global cellular mRNA in U-87 astrocytoma cells and primary astrocytes with a fold change > ±1.8 (p <0.01).

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: RNA Binding Assay, Sequencing

( A ) MRNA microarray validation with qRT-PCR analysis in grouped RISC-IP U-87 astrocytoma and primary astrocytes samples. Grouped RISC-IP data were compared to the grouped global mRNA from U-87 astrocytoma and primary astrocytes samples. Eight mRNAs were selected from the grouped mRNA microarray dataset and examined by qRT-PCR. Fold change from the mRNA microarray are given by log2 values (left y-axis, light grey bars). Fold change from the qRT-PCR was determined using the 2 -ΔΔCt method and all mRNA expression values were normalized to the beta-actin endogenous control (right y-axis, dark grey bars). Error bars represent the standard deviation of the mean (SD). Importantly, the fold change (y-axis) cannot be directly compared between assays due to differences in calculation methods, but the general trend of up-regulation and down-regulation can be compared. ( B ) MRNAs in RISC compared to the global cellular milieu in U-87 astrocytoma cells. MRNA expression in U-87 astrocytoma cells were normalized to primary astrocytes mRNA expression. All mRNAs had a fold change >2.5 and were significantly expressed (p<0.01). Green and red arrows indicate decreased and increased levels respectively.

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: ( A ) MRNA microarray validation with qRT-PCR analysis in grouped RISC-IP U-87 astrocytoma and primary astrocytes samples. Grouped RISC-IP data were compared to the grouped global mRNA from U-87 astrocytoma and primary astrocytes samples. Eight mRNAs were selected from the grouped mRNA microarray dataset and examined by qRT-PCR. Fold change from the mRNA microarray are given by log2 values (left y-axis, light grey bars). Fold change from the qRT-PCR was determined using the 2 -ΔΔCt method and all mRNA expression values were normalized to the beta-actin endogenous control (right y-axis, dark grey bars). Error bars represent the standard deviation of the mean (SD). Importantly, the fold change (y-axis) cannot be directly compared between assays due to differences in calculation methods, but the general trend of up-regulation and down-regulation can be compared. ( B ) MRNAs in RISC compared to the global cellular milieu in U-87 astrocytoma cells. MRNA expression in U-87 astrocytoma cells were normalized to primary astrocytes mRNA expression. All mRNAs had a fold change >2.5 and were significantly expressed (p<0.01). Green and red arrows indicate decreased and increased levels respectively.

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: Microarray, Quantitative RT-PCR, Expressing, Standard Deviation

RISC-immunoprecipitated  mRNA  in human U-87 astrocytoma cells compared to RISC-immunoprecipitated  mRNA  in primary human  astrocytes  with a fold change >±2.6 (p <0.01).

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: RISC-immunoprecipitated mRNA in human U-87 astrocytoma cells compared to RISC-immunoprecipitated mRNA in primary human astrocytes with a fold change >±2.6 (p <0.01).

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques:

Bar charts display the relative number (-log(p-value)) of mRNAs with a fold change >2.5 and were considered significant (p<0.01). RISC-IP mRNA were indicated with dark blue bars and the global mRNA were indicated with light blue bars. The threshold (yellow lines) were set at p<0.01 and were calculated using Fischer's exact p-value test using IPA software.

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: Bar charts display the relative number (-log(p-value)) of mRNAs with a fold change >2.5 and were considered significant (p<0.01). RISC-IP mRNA were indicated with dark blue bars and the global mRNA were indicated with light blue bars. The threshold (yellow lines) were set at p<0.01 and were calculated using Fischer's exact p-value test using IPA software.

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: Software

Bar charts display the relative number (-log(p-value)) of mRNAs with a fold change >2.5 and were considered significant (p<0.01). RISC-IP mRNA were indicated with dark blue bars and the global mRNA were indicated with light blue bars. The threshold (yellow lines) were set at p<0.01 and were calculated using Fischer's exact p-value test using IPA software.

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: Bar charts display the relative number (-log(p-value)) of mRNAs with a fold change >2.5 and were considered significant (p<0.01). RISC-IP mRNA were indicated with dark blue bars and the global mRNA were indicated with light blue bars. The threshold (yellow lines) were set at p<0.01 and were calculated using Fischer's exact p-value test using IPA software.

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: Software

Specific  messenger RNA  fold change linked to the increased levels of miR-34a in U-87  astrocytoma  RISC.

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: Specific messenger RNA fold change linked to the increased levels of miR-34a in U-87 astrocytoma RISC.

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: Permeability, Migration, Expressing, Binding Assay, Isolation

Specific  messenger RNA  fold change linked to increased levels of miR-195 in U-87  astrocytoma  RISC.

Journal: PLoS ONE

Article Title: The MicroRNA and MessengerRNA Profile of the RNA-Induced Silencing Complex in Human Primary Astrocyte and Astrocytoma Cells

doi: 10.1371/journal.pone.0013445

Figure Lengend Snippet: Specific messenger RNA fold change linked to increased levels of miR-195 in U-87 astrocytoma RISC.

Article Snippet: Gene expression microarray analyses of global mRNA and RISC-immunoprecipitated mRNA in primary human astrocytes and U-87 astrocytoma cells were outsourced to LC Sciences who are partnered with an Affymetrix® Authorized Service Provider, SeqWright DNA Technology Services (Houston, TX).

Techniques: Transduction

Target recognition by the miR-142-3p/−1 and miR-K10a/+1 5′-isomiRs. ( A , B ) Overlap of binding sites for the miR-142-3p and miR-K10a 5′-isomiRs identified in Ago2-PAR-CLIP data from ( A ) BC-1 and ( B ) BC-3 PEL cell lines . ( C ) Minimum base-pairing required for the miR-142-3p ( upper panel) and miR-K10a ( lower panel) 5′-isomiRs to share canonical binding sites. ( D ) Principal component analysis of microarray data of HEK293T cells transfected with individual 5′-isomiRs. ( E – I ) Sylamer enrichment landscape plots for 7mer 3′-UTR matches to miR-142-3p and miR-K10a 5′-isomiRs using microarray data from 293T cells transfected with individual miRNA mimics ( E – H , this study) or from published microarray data from miR-142 −/− mouse megakaryocytes (GEO data set GSE52141, ). The x -axis represents the ranked gene lists. miR-155 sites (pink and black lines) served as negative controls in addition to all random 7mers (gray). Enrichment plots for hexamer motifs are shown in Supplemental Figure S2.

Journal: RNA

Article Title: Divergent target recognition by coexpressed 5′-isomiRs of miR-142-3p and selective viral mimicry

doi: 10.1261/rna.048876.114

Figure Lengend Snippet: Target recognition by the miR-142-3p/−1 and miR-K10a/+1 5′-isomiRs. ( A , B ) Overlap of binding sites for the miR-142-3p and miR-K10a 5′-isomiRs identified in Ago2-PAR-CLIP data from ( A ) BC-1 and ( B ) BC-3 PEL cell lines . ( C ) Minimum base-pairing required for the miR-142-3p ( upper panel) and miR-K10a ( lower panel) 5′-isomiRs to share canonical binding sites. ( D ) Principal component analysis of microarray data of HEK293T cells transfected with individual 5′-isomiRs. ( E – I ) Sylamer enrichment landscape plots for 7mer 3′-UTR matches to miR-142-3p and miR-K10a 5′-isomiRs using microarray data from 293T cells transfected with individual miRNA mimics ( E – H , this study) or from published microarray data from miR-142 −/− mouse megakaryocytes (GEO data set GSE52141, ). The x -axis represents the ranked gene lists. miR-155 sites (pink and black lines) served as negative controls in addition to all random 7mers (gray). Enrichment plots for hexamer motifs are shown in Supplemental Figure S2.

Article Snippet: For an unbiased comparison of the regulatory potential of these isomiRs, we therefore performed Illumina microarray gene expression analyses of HEK293T cells transfected with mimics of the individual isomiRs.

Techniques: Binding Assay, Microarray, Transfection