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microarray analysis suite instrument system  (Thermo Fisher)


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    Thermo Fisher microarray analysis suite instrument system
    Principal component analysis of <t>microarray</t> data to demonstrate similarity of response of the cell types and treatment times. In the plot, each point represents a cell line (NHEK, Leuk1, Leuk2, or 101A) and treatment time (0 h, black circles; 24 h, gray triangles) of CSC exposure (25 μg/ml). The X, Y and Z-axes are PC#1, PC#2 and PC#3, respectively.
    Microarray Analysis Suite Instrument System, supplied by Thermo Fisher, 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/result/microarray analysis suite instrument system/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    microarray analysis suite instrument system - by Bioz Stars, 2026-03
    90/100 stars

    Images

    1) Product Images from "Cigarette smoke condensate induces cytochromes P450 and aldo-keto reductases in oral cancer cells"

    Article Title: Cigarette smoke condensate induces cytochromes P450 and aldo-keto reductases in oral cancer cells

    Journal: Toxicology letters

    doi: 10.1016/j.toxlet.2006.03.008

    Principal component analysis of microarray data to demonstrate similarity of response of the cell types and treatment times. In the plot, each point represents a cell line (NHEK, Leuk1, Leuk2, or 101A) and treatment time (0 h, black circles; 24 h, gray triangles) of CSC exposure (25 μg/ml). The X, Y and Z-axes are PC#1, PC#2 and PC#3, respectively.
    Figure Legend Snippet: Principal component analysis of microarray data to demonstrate similarity of response of the cell types and treatment times. In the plot, each point represents a cell line (NHEK, Leuk1, Leuk2, or 101A) and treatment time (0 h, black circles; 24 h, gray triangles) of CSC exposure (25 μg/ml). The X, Y and Z-axes are PC#1, PC#2 and PC#3, respectively.

    Techniques Used: Microarray

    Comparative quantitative real-time RT-PCR analysis. RNA from control (0 h) and treated (24 h, 25 μg/ml CSC) cells were subjected to quantitative real-time RT-PCR analysis using primers specific for CYP1A1, CYP1B1, AKR1C1, AKR1C3, AKR1B10, and the internal standard β-actin. (A) NHEK; (B) Leuk1; (C) Leuk2; (D) 101A cells; open bars, microarray data; solid bars, RT-PCR data. The fold change levels on the Y-axis are relative to the expression in untreated cells. Results are expressed as the mean and range of duplicate determinations for microarray data, and as mean ± S.D. of four independent experiments for qRT-PCR data: *p < 0.05; **p = 0.01; #non-significant.
    Figure Legend Snippet: Comparative quantitative real-time RT-PCR analysis. RNA from control (0 h) and treated (24 h, 25 μg/ml CSC) cells were subjected to quantitative real-time RT-PCR analysis using primers specific for CYP1A1, CYP1B1, AKR1C1, AKR1C3, AKR1B10, and the internal standard β-actin. (A) NHEK; (B) Leuk1; (C) Leuk2; (D) 101A cells; open bars, microarray data; solid bars, RT-PCR data. The fold change levels on the Y-axis are relative to the expression in untreated cells. Results are expressed as the mean and range of duplicate determinations for microarray data, and as mean ± S.D. of four independent experiments for qRT-PCR data: *p < 0.05; **p = 0.01; #non-significant.

    Techniques Used: Quantitative RT-PCR, Microarray, Reverse Transcription Polymerase Chain Reaction, Expressing

    CSC-induced expression increases for selected target genes. (A) Basal expression levels in untreated cell lines NHEK, Leuk1, Leuk2, and 101A for the indicated target genes, as measured by microarray-derived target intensities. (B) Time course of induction. For each cell line, target intensities after CSC treatment for 0, 5, and 24 h are plotted for the following genes: CYP1A1 (□); CYP1B1 (▲); AKR1C1 (▼); AKR1C3 (■); AKR1B10 (○).
    Figure Legend Snippet: CSC-induced expression increases for selected target genes. (A) Basal expression levels in untreated cell lines NHEK, Leuk1, Leuk2, and 101A for the indicated target genes, as measured by microarray-derived target intensities. (B) Time course of induction. For each cell line, target intensities after CSC treatment for 0, 5, and 24 h are plotted for the following genes: CYP1A1 (□); CYP1B1 (▲); AKR1C1 (▼); AKR1C3 (■); AKR1B10 (○).

    Techniques Used: Expressing, Microarray, Derivative Assay



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    microarray analysis suite instrument system  (Thermo Fisher)
    90
    Thermo Fisher microarray analysis suite instrument system
    Principal component analysis of <t>microarray</t> data to demonstrate similarity of response of the cell types and treatment times. In the plot, each point represents a cell line (NHEK, Leuk1, Leuk2, or 101A) and treatment time (0 h, black circles; 24 h, gray triangles) of CSC exposure (25 μg/ml). The X, Y and Z-axes are PC#1, PC#2 and PC#3, respectively.
    Microarray Analysis Suite Instrument System, supplied by Thermo Fisher, 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/result/microarray analysis suite instrument system/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    microarray analysis suite instrument system - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Principal component analysis of microarray data to demonstrate similarity of response of the cell types and treatment times. In the plot, each point represents a cell line (NHEK, Leuk1, Leuk2, or 101A) and treatment time (0 h, black circles; 24 h, gray triangles) of CSC exposure (25 μg/ml). The X, Y and Z-axes are PC#1, PC#2 and PC#3, respectively.

    Journal: Toxicology letters

    Article Title: Cigarette smoke condensate induces cytochromes P450 and aldo-keto reductases in oral cancer cells

    doi: 10.1016/j.toxlet.2006.03.008

    Figure Lengend Snippet: Principal component analysis of microarray data to demonstrate similarity of response of the cell types and treatment times. In the plot, each point represents a cell line (NHEK, Leuk1, Leuk2, or 101A) and treatment time (0 h, black circles; 24 h, gray triangles) of CSC exposure (25 μg/ml). The X, Y and Z-axes are PC#1, PC#2 and PC#3, respectively.

    Article Snippet: Microarray procedures Micoarray expression analysis was performed on a Microarray Analysis Suite instrument system (Affymetrix, Santa Clara, CA).

    Techniques: Microarray

    Comparative quantitative real-time RT-PCR analysis. RNA from control (0 h) and treated (24 h, 25 μg/ml CSC) cells were subjected to quantitative real-time RT-PCR analysis using primers specific for CYP1A1, CYP1B1, AKR1C1, AKR1C3, AKR1B10, and the internal standard β-actin. (A) NHEK; (B) Leuk1; (C) Leuk2; (D) 101A cells; open bars, microarray data; solid bars, RT-PCR data. The fold change levels on the Y-axis are relative to the expression in untreated cells. Results are expressed as the mean and range of duplicate determinations for microarray data, and as mean ± S.D. of four independent experiments for qRT-PCR data: *p < 0.05; **p = 0.01; #non-significant.

    Journal: Toxicology letters

    Article Title: Cigarette smoke condensate induces cytochromes P450 and aldo-keto reductases in oral cancer cells

    doi: 10.1016/j.toxlet.2006.03.008

    Figure Lengend Snippet: Comparative quantitative real-time RT-PCR analysis. RNA from control (0 h) and treated (24 h, 25 μg/ml CSC) cells were subjected to quantitative real-time RT-PCR analysis using primers specific for CYP1A1, CYP1B1, AKR1C1, AKR1C3, AKR1B10, and the internal standard β-actin. (A) NHEK; (B) Leuk1; (C) Leuk2; (D) 101A cells; open bars, microarray data; solid bars, RT-PCR data. The fold change levels on the Y-axis are relative to the expression in untreated cells. Results are expressed as the mean and range of duplicate determinations for microarray data, and as mean ± S.D. of four independent experiments for qRT-PCR data: *p < 0.05; **p = 0.01; #non-significant.

    Article Snippet: Microarray procedures Micoarray expression analysis was performed on a Microarray Analysis Suite instrument system (Affymetrix, Santa Clara, CA).

    Techniques: Quantitative RT-PCR, Microarray, Reverse Transcription Polymerase Chain Reaction, Expressing

    CSC-induced expression increases for selected target genes. (A) Basal expression levels in untreated cell lines NHEK, Leuk1, Leuk2, and 101A for the indicated target genes, as measured by microarray-derived target intensities. (B) Time course of induction. For each cell line, target intensities after CSC treatment for 0, 5, and 24 h are plotted for the following genes: CYP1A1 (□); CYP1B1 (▲); AKR1C1 (▼); AKR1C3 (■); AKR1B10 (○).

    Journal: Toxicology letters

    Article Title: Cigarette smoke condensate induces cytochromes P450 and aldo-keto reductases in oral cancer cells

    doi: 10.1016/j.toxlet.2006.03.008

    Figure Lengend Snippet: CSC-induced expression increases for selected target genes. (A) Basal expression levels in untreated cell lines NHEK, Leuk1, Leuk2, and 101A for the indicated target genes, as measured by microarray-derived target intensities. (B) Time course of induction. For each cell line, target intensities after CSC treatment for 0, 5, and 24 h are plotted for the following genes: CYP1A1 (□); CYP1B1 (▲); AKR1C1 (▼); AKR1C3 (■); AKR1B10 (○).

    Article Snippet: Microarray procedures Micoarray expression analysis was performed on a Microarray Analysis Suite instrument system (Affymetrix, Santa Clara, CA).

    Techniques: Expressing, Microarray, Derivative Assay