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gene chip 7g microarray scanner  (Thermo Fisher)


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    Structured Review

    Thermo Fisher gene chip 7g microarray scanner
    Selected transcripts clustered and validated with real-time PCR. After pathway analysis, we selected genes involved in major pathways (the common pathways in Tables and ). First, selected genes were clustered using Cluster 3.0 according to the LOG value ((a)–(c)). Red is relatively upregulated and green is relatively downregulated in different samples. The three “Cs” are the three blank control samples. The three “Ms” are the model control samples. The three “Es” are the EA + model samples. Then, to verify the reliability of the <t>microarray</t> analysis, we verified these selected genes from the clustering diagram using quantitative real-time RT-PCR. Gene expressions in blank control group, model control group, and EA + model group were presented in ((d)–(g)). These transcripts analyzed here showed coherent profiles with cluster ((a)–(c)). Note: ★★ P < 0.01, versus blank control group; ☆ P < 0.05 and ☆☆ P < 0.01, versus model control group.
    Gene Chip 7g Microarray Scanner, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/gene chip 7g microarray scanner/product/Thermo Fisher
    Average 86 stars, based on 1 article reviews
    gene chip 7g microarray scanner - by Bioz Stars, 2026-02
    86/100 stars

    Images

    1) Product Images from "A Study on Effect of Electroacupuncture on Gene Expression in Hypothalamus of Rats with Stress-Induced Prehypertension Based on Gene Chip Technology"

    Article Title: A Study on Effect of Electroacupuncture on Gene Expression in Hypothalamus of Rats with Stress-Induced Prehypertension Based on Gene Chip Technology

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    doi: 10.1155/2015/621237

    Selected transcripts clustered and validated with real-time PCR. After pathway analysis, we selected genes involved in major pathways (the common pathways in Tables and ). First, selected genes were clustered using Cluster 3.0 according to the LOG value ((a)–(c)). Red is relatively upregulated and green is relatively downregulated in different samples. The three “Cs” are the three blank control samples. The three “Ms” are the model control samples. The three “Es” are the EA + model samples. Then, to verify the reliability of the microarray analysis, we verified these selected genes from the clustering diagram using quantitative real-time RT-PCR. Gene expressions in blank control group, model control group, and EA + model group were presented in ((d)–(g)). These transcripts analyzed here showed coherent profiles with cluster ((a)–(c)). Note: ★★ P < 0.01, versus blank control group; ☆ P < 0.05 and ☆☆ P < 0.01, versus model control group.
    Figure Legend Snippet: Selected transcripts clustered and validated with real-time PCR. After pathway analysis, we selected genes involved in major pathways (the common pathways in Tables and ). First, selected genes were clustered using Cluster 3.0 according to the LOG value ((a)–(c)). Red is relatively upregulated and green is relatively downregulated in different samples. The three “Cs” are the three blank control samples. The three “Ms” are the model control samples. The three “Es” are the EA + model samples. Then, to verify the reliability of the microarray analysis, we verified these selected genes from the clustering diagram using quantitative real-time RT-PCR. Gene expressions in blank control group, model control group, and EA + model group were presented in ((d)–(g)). These transcripts analyzed here showed coherent profiles with cluster ((a)–(c)). Note: ★★ P < 0.01, versus blank control group; ☆ P < 0.05 and ☆☆ P < 0.01, versus model control group.

    Techniques Used: Real-time Polymerase Chain Reaction, Microarray, Quantitative RT-PCR



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    gene chip 7g microarray scanner  (Thermo Fisher)
    86
    Thermo Fisher gene chip 7g microarray scanner
    Selected transcripts clustered and validated with real-time PCR. After pathway analysis, we selected genes involved in major pathways (the common pathways in Tables and ). First, selected genes were clustered using Cluster 3.0 according to the LOG value ((a)–(c)). Red is relatively upregulated and green is relatively downregulated in different samples. The three “Cs” are the three blank control samples. The three “Ms” are the model control samples. The three “Es” are the EA + model samples. Then, to verify the reliability of the <t>microarray</t> analysis, we verified these selected genes from the clustering diagram using quantitative real-time RT-PCR. Gene expressions in blank control group, model control group, and EA + model group were presented in ((d)–(g)). These transcripts analyzed here showed coherent profiles with cluster ((a)–(c)). Note: ★★ P < 0.01, versus blank control group; ☆ P < 0.05 and ☆☆ P < 0.01, versus model control group.
    Gene Chip 7g Microarray Scanner, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/gene chip 7g microarray scanner/product/Thermo Fisher
    Average 86 stars, based on 1 article reviews
    gene chip 7g microarray scanner - by Bioz Stars, 2026-02
    86/100 stars
    		  Buy from Supplier

    Image Search Results


    Selected transcripts clustered and validated with real-time PCR. After pathway analysis, we selected genes involved in major pathways (the common pathways in Tables and ). First, selected genes were clustered using Cluster 3.0 according to the LOG value ((a)–(c)). Red is relatively upregulated and green is relatively downregulated in different samples. The three “Cs” are the three blank control samples. The three “Ms” are the model control samples. The three “Es” are the EA + model samples. Then, to verify the reliability of the microarray analysis, we verified these selected genes from the clustering diagram using quantitative real-time RT-PCR. Gene expressions in blank control group, model control group, and EA + model group were presented in ((d)–(g)). These transcripts analyzed here showed coherent profiles with cluster ((a)–(c)). Note: ★★ P < 0.01, versus blank control group; ☆ P < 0.05 and ☆☆ P < 0.01, versus model control group.

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    Article Title: A Study on Effect of Electroacupuncture on Gene Expression in Hypothalamus of Rats with Stress-Induced Prehypertension Based on Gene Chip Technology

    doi: 10.1155/2015/621237

    Figure Lengend Snippet: Selected transcripts clustered and validated with real-time PCR. After pathway analysis, we selected genes involved in major pathways (the common pathways in Tables and ). First, selected genes were clustered using Cluster 3.0 according to the LOG value ((a)–(c)). Red is relatively upregulated and green is relatively downregulated in different samples. The three “Cs” are the three blank control samples. The three “Ms” are the model control samples. The three “Es” are the EA + model samples. Then, to verify the reliability of the microarray analysis, we verified these selected genes from the clustering diagram using quantitative real-time RT-PCR. Gene expressions in blank control group, model control group, and EA + model group were presented in ((d)–(g)). These transcripts analyzed here showed coherent profiles with cluster ((a)–(c)). Note: ★★ P < 0.01, versus blank control group; ☆ P < 0.05 and ☆☆ P < 0.01, versus model control group.

    Article Snippet: Total RNA of each sample was used for labeling and array hybridization in the following steps. (1) Prepare the poly-A RNA controls. (2) Synthesize first-strand cDNA. (3) Synthesize second-strand cDNA. (4) Synthesize cRNA by in vitro transcription. (5) Synthesize 2nd-cycle cDNA. (6) Hydrolyze using RNase H. (7) Fragment and label the single-stranded cDNA. (8) Array hybridization using the Affymetrix Gene Chip 645 System followed by washing with the Affymetrix Gene Chip 450 System. (9) Array scanning using the Affymetrix Gene Chip 7G microarray scanner (Affymetrix, USA).

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