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CapitalBio Corporation smartarray chips
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.
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
https://www.bioz.com/product/smartarray+chips/smartarraytm+microarrayer/pmc03650049-90-0-1
Average 90 stars, based on 1 article reviews
smartarray chips - by Bioz Stars, 2026-09
90/100 stars

Images

1) Product Images from "Low Dose Decitabine Treatment Induces CD80 Expression in Cancer Cells and Stimulates Tumor Specific Cytotoxic T Lymphocyte Responses"

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

Journal: PLoS ONE

doi: 10.1371/journal.pone.0062924

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.
Figure Legend 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.

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

Related Articles

other:

Article Title: Microarray-based gene expression profiles in multiple tissues of the domesticated silkworm, Bombyx mori
Article Snippet: The probes were dissolved in EasyArrayTM spotting solution (CapitalBio Corp.) at 40 μM and finally spotted on aminosilane coated slides using a SmartArrayTM microarrayer (CapitalBio Corp.).

Article Title: Comparative and functional genomics reveals genetic diversity and determinants of host specificity among reference strains and a large collection of Chinese isolates of the phytopathogen Xanthomonas campestris pv. campestris
Article Snippet: PCR products and 70-mer oligonucleotides (20 μM) were printed on amino silaned glass slides (CapitalBio Corp.) using a SmartArrayTM microarrayer (CapitalBio Corp.).

Polymerase Chain Reaction:

Article Title: Environmentally Relevant Concentrations of Carbamazepine Caused Endocrine-Disrupting Effects on Nontarget Organisms, Chinese Rare Minnows (Gobiocypris rarus).
Article Snippet: In the present study, Chinese rare minnows (Gobiocypris rarus) were 16 exposed to 1, 10, and 100 μg/L carbamazepine (CBZ) under flow-through conditions 17 for 28 d. A hepatic-specific custom microarray identified 111 and 71 differentially 18 expressed genes in the livers of females and males exposed to 100 μg/L CBZ, 19 respectively (ratio ≥ 2, p ≤ 0.05).. The levels of five differentially expressed genes 20 associated with the hypothalamic-pituitary-gonadal (HPG) axis were quantified by 21 qPCR, and the results indicated the feasibility of screening endocrine-disrupting 22 chemicals using a custom microarray.. The mRNA levels of genes related to the HPG 23 axis differed significantly in different organs of Chinese rare minnow (p<0.05).

Labeling:

Article Title: Differential expression profiles of microRNAs in highly and weakly invasive/metastatic pancreatic cancer cells.
Article Snippet: .. These probes were labeled onto a 75x25 mm chemically-modified plate using the SmartArrayTM microarray system (CapitalBio Technology, Inc.). .. The samples also contained two endogenous controls (U6, tRNA), eight exogenous controls (Zip5, Zip13, Zip15, Zip21, Zip23, Zip25, Y2 and Y3; Ambion; Thermo Fisher Scientific, Inc.), a positive control (HEX), and a hybridization negative control (50% dimethyl sulfoxide).

Article Title: Differential expression profiles of microRNAs in highly and weakly invasive/metastatic pancreatic cancer cells
Article Snippet: .. These probes were labeled onto a 75×25 mm chemically-modified plate using the SmartArray TM microarray system (CapitalBio Technology, Inc.). .. The samples also contained two endogenous controls (U6, tRNA), eight exogenous controls (Zip5, Zip13, Zip15, Zip21, Zip23, Zip25, Y2 and Y3; Ambion; Thermo Fisher Scientific, Inc.), a positive control (HEX), and a hybridization negative control (50% dimethyl sulfoxide).

Microarray:

Article Title: Differential expression profiles of microRNAs in highly and weakly invasive/metastatic pancreatic cancer cells.
Article Snippet: .. These probes were labeled onto a 75x25 mm chemically-modified plate using the SmartArrayTM microarray system (CapitalBio Technology, Inc.). .. The samples also contained two endogenous controls (U6, tRNA), eight exogenous controls (Zip5, Zip13, Zip15, Zip21, Zip23, Zip25, Y2 and Y3; Ambion; Thermo Fisher Scientific, Inc.), a positive control (HEX), and a hybridization negative control (50% dimethyl sulfoxide).

Article Title: Differential expression profiles of microRNAs in highly and weakly invasive/metastatic pancreatic cancer cells
Article Snippet: .. These probes were labeled onto a 75×25 mm chemically-modified plate using the SmartArray TM microarray system (CapitalBio Technology, Inc.). .. The samples also contained two endogenous controls (U6, tRNA), eight exogenous controls (Zip5, Zip13, Zip15, Zip21, Zip23, Zip25, Y2 and Y3; Ambion; Thermo Fisher Scientific, Inc.), a positive control (HEX), and a hybridization negative control (50% dimethyl sulfoxide).

Article Title: Systematical Analysis of the Protein Targets of Lactoferricin B and Histatin-5 Using Yeast Proteome Microarrays
Article Snippet: In a cold room, the individual proteins and landmarks were printed in duplicate on aldehyde-coated glass slides by using CapitalBio SmartArrayerTM 136 (CapitalBio Corporation, Beijing, China). .. CapitalBio SmartArrayer is a high-throughput microarray spotter with 48 pins and print 48 proteins at the same time. ..

Concentration Assay:

Article Title: Comparative Analysis for Glycopatterns and Complex-Type N- Glycans of Glycoprotein in Sera from Chronic Hepatitis B- and C-Infected Patients
Article Snippet: A lectin microarray was produced using 37 lectins [purchased from Vector Laboratories, Sigma-Aldrich (St Louis, MO) and Calbiochem (Billerica, MA)] with different binding preferences covering N- and O- linked glycan according to our previous protocol (Qin et al., ). .. Briefly, 37 lectins were dissolved in the manufacturer's recommended buffer containing 1 mmol/L of the appropriate monosaccharide at a concentration of 1 mg/mL and were spotted on the homemade epoxysilane-coated slides with Stealth micro-spotting pins (SMP-10B; TeleChem, Sunnyvale, CA) by a Capital smart microarrayer (CapitalBio, Beijing, China). ..



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CapitalBio Corporation smartarray microarray chips capitalbio beijing china
<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.
Smartarray Microarray Chips Capitalbio Beijing China, 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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<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.
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
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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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CapitalBio Corporation smartarray chips
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.
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
https://www.bioz.com/product/smartarray+chips/smartarraytm+microarrayer/pmc03650049-90-0-1
Average 90 stars, based on 1 article reviews
smartarray chips - by Bioz Stars, 2026-09
90/100 stars
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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