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27k rat genome array chips smartarray tm  (CapitalBio Corporation)

 
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    CapitalBio Corporation 27k rat genome array chips smartarray tm
    27k Rat Genome Array Chips Smartarray Tm, supplied by CapitalBio Corporation, 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/smartarray+chips/27+k+rat+genome+oligo+arrays/pmc04237099-91-1-9
    Average 90 stars, based on 1 article reviews
    27k rat genome array chips smartarray tm - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Labeling:

    Article Title: Gene Expression Profiles at Moxibustioned Site (ST36): A Microarray Analysis
    Article Snippet: Universal rat reference RNA purchased from Stratagene was also labeled as common reference control. .. RNA from sample and common reference were fluorescently labeled by Cy5 or Cy3, respectively, and then were hybridized paired to 27K Rat Genome Array (CapitalBio, China). ..

    other:

    Article Title: Microvascular endothelial cells play potential immunoregulatory roles in the immune response to foot-and-mouth disease vaccines.
    Article Snippet: Microvascular endothelial cells (MVECs) have been documented to have important immunoregulatory effects.. Exploring their roles in the immune response to foot‐and‐mouth disease (FMD) vaccines would help to improve their efficacy.. In this study, the effects of FMD vaccine 146s antigens on gene expression profiles of rat intestinal mucosal and myocardial MVECs were analysed using microarray, and their effects on transendothelial migration (TEM) of peripheral blood mononuclear cells (PBMC) were investigated by the Transwell migration assay.

    Article Title: Hippocampal gene expression in a rat model of depression after electroacupuncture at the Baihui and Yintang acupoints
    Article Snippet: The labeled sample was dissolved in 80 μL hybridization solution (3 × SSC, 0.2% SDS, 5 × Denhardt's solution, 25% fluoroamine) and hybridized to a 27K Rat Genome Array gene-chip (CapitalBio Corporation; Rat Genome Version 3.0.5) at 42°C overnight.

    Gene Expression:

    Article Title: Systematic profiling of mRNA and miRNA expression in the pancreatic islets of spontaneously diabetic Goto-Kakizaki rats
    Article Snippet: .. The 27K Rat Genome Array chips (SmartArray TM , CapitalBio Corp), were used to profile gene expression in islets from GK/Wistar rats according to the manufacturer’s instructions. .. Briefly, RNA from three GK or Wistar rat islets was mixed into a pool, respectively and the total RNA samples (100 ng) were reversely transcribed using Moloney Murine leukemia virus (Takara Chemicals, Shiga, Japan) and amplified by an in vitro transcription based method.

    Article Title: A microarray gene analysis of peripheral whole blood in normal adult male rats after long-term GH gene therapy
    Article Snippet: .. We determined the global gene expression profile of peripheral whole blood from normal adult male rats after long-term GH gene therapy using CapitalBio 27 K Rat Genome Oligo Arrays. .. Sixty one genes were found to be differentially expressed in GH gene-treated rats 24 weeks after receiving GH gene therapy, at a two-fold higher or lower level compared to the empty vector group (p < 0.05).

    Microarray:

    Article Title: Transcriptome Analysis of the Hippocampus in Novel Rat Model of Febrile Seizures
    Article Snippet: Samples were purified using a Qiagen RNeasy Kit (Qiagen, Germany). .. Microarray analysis was performed at CapitalBio Corporation (SBC, China) using Whole Rat Genome Oligo nucleotide 4×44 k Microarrays (Agilent, CA, USA). .. The quality of cyanine-labeled cRNA samples, including yield, concentration, amplification efficiency and abundance of cyanine fluorophore, was determined by an ND-1000 spectrophotometer (Nanodrop, USA) at A260 and A280.

    Article Title: Hnrnpk, a protein differentially expressed in immature rat ovarian development, is required for normal primordial follicle assembly and development.
    Article Snippet: .. To compare the differentially expressed genes in the ovaries treated with the three individual Hnrnpk siRNAs and the control, a twochannel microarray was performed at CapitalBio Corp. (Bejing, China) using the 22K Rat Genome Array (30). .. Briefly, Hnrnpk siRNAs cDNA labeled by Cy5-camptothecin and the controls labeled by Cy3-camptothecin (Takara, Otsu, Japan).

    Control:

    Article Title: Hnrnpk, a protein differentially expressed in immature rat ovarian development, is required for normal primordial follicle assembly and development.
    Article Snippet: .. To compare the differentially expressed genes in the ovaries treated with the three individual Hnrnpk siRNAs and the control, a twochannel microarray was performed at CapitalBio Corp. (Bejing, China) using the 22K Rat Genome Array (30). .. Briefly, Hnrnpk siRNAs cDNA labeled by Cy5-camptothecin and the controls labeled by Cy3-camptothecin (Takara, Otsu, Japan).

    Generated:

    Article Title: Xueshuan Xinmaining Tablet Treats Blood Stasis through Regulating the Expression of F13a1, Car1, and Tbxa2r
    Article Snippet: .. The rat genome oligonucleotide set was generated using 27K Rat Genome Array (CapitalBio's prespotted high-density pairwise oligonucleotide microarrays, version 3.0 CapitalBio Corp., Beijing, China). ..



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    smartarray microarray chips capitalbio beijing china  (CapitalBio Corporation)
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    <t>Microarray</t> analysis uncovered an altered and specific transcriptional profile underlying the cell shape change and the suppression of the metastatic potential by Runx3. ( A ) Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) annotations assigned different repertoires of differentially expressed genes (DEGs) that were regulated by Runx3 in B16-F10 cells and, in the case of B16-F0 cells vs. B16-F10 cells, to the terms relevant to the actin cytoskeleton and adhesion. Each GO/KEGG annotation term is inscribed as a caption. The number of DEGs within a repertoire is described at x axis. The columns for the downregulated and the upregulated DEGs are shown in different colors as explained at the top of the figure., Down/Up by Runx3 indicates the appearance of DEGs in the case of B16-F10/Runx3 cells vs. mock control B16-F10 cells. Down/Up in B16-F0 indicates the appearance of DEGs in the case of B16-F0 cells vs. B16-F10 cells. Down/Up in common indicates the appearance of same DEGs in both cases. ( B ) Runx3 upregulated the expression of extracellular matrix (ECM) genes. The summary table indicates the gene names and their corresponding fold changes. ( C ) Runx3 regulated the expression of a list of DEGs that were inversely associated with an increase in the metastatic potential of B16-F10 cells compared to B16-F0 cells. The heatmap shows the gene names and their fold changes in the cases of B16-F10/Runx3 cells vs. mock control B16-F10 cells and B16-F0 cells vs. B16-F10 cells, respectively.
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    27k rat genome array chips smartarray tm  (CapitalBio Corporation)
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    <t>Microarray</t> analysis uncovered an altered and specific transcriptional profile underlying the cell shape change and the suppression of the metastatic potential by Runx3. ( A ) Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) annotations assigned different repertoires of differentially expressed genes (DEGs) that were regulated by Runx3 in B16-F10 cells and, in the case of B16-F0 cells vs. B16-F10 cells, to the terms relevant to the actin cytoskeleton and adhesion. Each GO/KEGG annotation term is inscribed as a caption. The number of DEGs within a repertoire is described at x axis. The columns for the downregulated and the upregulated DEGs are shown in different colors as explained at the top of the figure., Down/Up by Runx3 indicates the appearance of DEGs in the case of B16-F10/Runx3 cells vs. mock control B16-F10 cells. Down/Up in B16-F0 indicates the appearance of DEGs in the case of B16-F0 cells vs. B16-F10 cells. Down/Up in common indicates the appearance of same DEGs in both cases. ( B ) Runx3 upregulated the expression of extracellular matrix (ECM) genes. The summary table indicates the gene names and their corresponding fold changes. ( C ) Runx3 regulated the expression of a list of DEGs that were inversely associated with an increase in the metastatic potential of B16-F10 cells compared to B16-F0 cells. The heatmap shows the gene names and their fold changes in the cases of B16-F10/Runx3 cells vs. mock control B16-F10 cells and B16-F0 cells vs. B16-F10 cells, respectively.
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    dual-channel smartarray chips  (CapitalBio Corporation)
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    <t>Microarray</t> analysis uncovered an altered and specific transcriptional profile underlying the cell shape change and the suppression of the metastatic potential by Runx3. ( A ) Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) annotations assigned different repertoires of differentially expressed genes (DEGs) that were regulated by Runx3 in B16-F10 cells and, in the case of B16-F0 cells vs. B16-F10 cells, to the terms relevant to the actin cytoskeleton and adhesion. Each GO/KEGG annotation term is inscribed as a caption. The number of DEGs within a repertoire is described at x axis. The columns for the downregulated and the upregulated DEGs are shown in different colors as explained at the top of the figure., Down/Up by Runx3 indicates the appearance of DEGs in the case of B16-F10/Runx3 cells vs. mock control B16-F10 cells. Down/Up in B16-F0 indicates the appearance of DEGs in the case of B16-F0 cells vs. B16-F10 cells. Down/Up in common indicates the appearance of same DEGs in both cases. ( B ) Runx3 upregulated the expression of extracellular matrix (ECM) genes. The summary table indicates the gene names and their corresponding fold changes. ( C ) Runx3 regulated the expression of a list of DEGs that were inversely associated with an increase in the metastatic potential of B16-F10 cells compared to B16-F0 cells. The heatmap shows the gene names and their fold changes in the cases of B16-F10/Runx3 cells vs. mock control B16-F10 cells and B16-F0 cells vs. B16-F10 cells, respectively.
    Dual Channel Smartarray Chips, supplied by CapitalBio Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    smartarray chips  (CapitalBio Corporation)
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    The mouse <t>SmartArray</t> chips were hybridized with RNA derived from DAC or PBS treated EL4 cells. (A) Heatmap of some upregulated genes by DAC treatment. Columns represent microarray data obtained from 3 independent biological replicates. (B) RT-PCR was used to validate the up-regulated genes. (C) qRT-PCR was used to quantify up-regulated genes in DAC and PBS treated EL4 cells.
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    Image Search Results


    Microarray analysis uncovered an altered and specific transcriptional profile underlying the cell shape change and the suppression of the metastatic potential by Runx3. ( A ) Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) annotations assigned different repertoires of differentially expressed genes (DEGs) that were regulated by Runx3 in B16-F10 cells and, in the case of B16-F0 cells vs. B16-F10 cells, to the terms relevant to the actin cytoskeleton and adhesion. Each GO/KEGG annotation term is inscribed as a caption. The number of DEGs within a repertoire is described at x axis. The columns for the downregulated and the upregulated DEGs are shown in different colors as explained at the top of the figure., Down/Up by Runx3 indicates the appearance of DEGs in the case of B16-F10/Runx3 cells vs. mock control B16-F10 cells. Down/Up in B16-F0 indicates the appearance of DEGs in the case of B16-F0 cells vs. B16-F10 cells. Down/Up in common indicates the appearance of same DEGs in both cases. ( B ) Runx3 upregulated the expression of extracellular matrix (ECM) genes. The summary table indicates the gene names and their corresponding fold changes. ( C ) Runx3 regulated the expression of a list of DEGs that were inversely associated with an increase in the metastatic potential of B16-F10 cells compared to B16-F0 cells. The heatmap shows the gene names and their fold changes in the cases of B16-F10/Runx3 cells vs. mock control B16-F10 cells and B16-F0 cells vs. B16-F10 cells, respectively.

    Journal: International Journal of Molecular Sciences

    Article Title: Runx3 Induces a Cell Shape Change and Suppresses Migration and Metastasis of Melanoma Cells by Altering a Transcriptional Profile

    doi: 10.3390/ijms22042219

    Figure Lengend Snippet: Microarray analysis uncovered an altered and specific transcriptional profile underlying the cell shape change and the suppression of the metastatic potential by Runx3. ( A ) Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) annotations assigned different repertoires of differentially expressed genes (DEGs) that were regulated by Runx3 in B16-F10 cells and, in the case of B16-F0 cells vs. B16-F10 cells, to the terms relevant to the actin cytoskeleton and adhesion. Each GO/KEGG annotation term is inscribed as a caption. The number of DEGs within a repertoire is described at x axis. The columns for the downregulated and the upregulated DEGs are shown in different colors as explained at the top of the figure., Down/Up by Runx3 indicates the appearance of DEGs in the case of B16-F10/Runx3 cells vs. mock control B16-F10 cells. Down/Up in B16-F0 indicates the appearance of DEGs in the case of B16-F0 cells vs. B16-F10 cells. Down/Up in common indicates the appearance of same DEGs in both cases. ( B ) Runx3 upregulated the expression of extracellular matrix (ECM) genes. The summary table indicates the gene names and their corresponding fold changes. ( C ) Runx3 regulated the expression of a list of DEGs that were inversely associated with an increase in the metastatic potential of B16-F10 cells compared to B16-F0 cells. The heatmap shows the gene names and their fold changes in the cases of B16-F10/Runx3 cells vs. mock control B16-F10 cells and B16-F0 cells vs. B16-F10 cells, respectively.

    Article Snippet: SmartArray microarray chips (CapitalBio, Beijing, China) were prepared from 32K Mouse Genome Array version 4.0 ( http://www.Operon.com , accessed on 25 April 2011).

    Techniques: Microarray, Control, Expressing

    The mouse SmartArray chips were hybridized with RNA derived from DAC or PBS treated EL4 cells. (A) Heatmap of some upregulated genes by DAC treatment. Columns represent microarray data obtained from 3 independent biological replicates. (B) RT-PCR was used to validate the up-regulated genes. (C) qRT-PCR was used to quantify up-regulated genes in DAC and PBS treated EL4 cells.

    Journal: PLoS ONE

    Article Title: Low Dose Decitabine Treatment Induces CD80 Expression in Cancer Cells and Stimulates Tumor Specific Cytotoxic T Lymphocyte Responses

    doi: 10.1371/journal.pone.0062924

    Figure Lengend Snippet: The mouse SmartArray chips were hybridized with RNA derived from DAC or PBS treated EL4 cells. (A) Heatmap of some upregulated genes by DAC treatment. Columns represent microarray data obtained from 3 independent biological replicates. (B) RT-PCR was used to validate the up-regulated genes. (C) qRT-PCR was used to quantify up-regulated genes in DAC and PBS treated EL4 cells.

    Article Snippet: SmartArray (CapitalBio, Beijing, China) chips containing about 25000 mouse genes were hybridized with labeled cDNA probes on a GeneChip system.

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