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Arraystar inc human gene expression microarray
Human Gene Expression Microarray, supplied by Arraystar inc, 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/microarray+for+gene+expression+analysis/human+gene+expression+microarray/pm39881131-132-35-45
Average 90 stars, based on 1 article reviews
human gene expression microarray - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Labeling:

Article Title: KIF26B, a novel oncogene, promotes proliferation and metastasis by activating the VEGF pathway in gastric cancer.
Article Snippet: Tumor metastasis is the main reason of cancer-related death for gastric cancer (GC) patients and gene expression microarray data indicate that kinesin family member 26B (KIF26B) is one of the most upregulated genes in metastatic GC samples.. Specifically, KIF26B expression was upregulated in a stepwise manner from non-tumorous gastric mucosa, primary GC tissues without metastasis, via primary GC tissues with metastasis, to secondary lymph node metastatic (LNM) foci.. Increased expression of KIF26B was correlated with tumor size, positive LNM or distant metastases and poor prognosis.

Gene Expression:

Article Title: KIF26B, a novel oncogene, promotes proliferation and metastasis by activating the VEGF pathway in gastric cancer.
Article Snippet: Tumor metastasis is the main reason of cancer-related death for gastric cancer (GC) patients and gene expression microarray data indicate that kinesin family member 26B (KIF26B) is one of the most upregulated genes in metastatic GC samples.. Specifically, KIF26B expression was upregulated in a stepwise manner from non-tumorous gastric mucosa, primary GC tissues without metastasis, via primary GC tissues with metastasis, to secondary lymph node metastatic (LNM) foci.. Increased expression of KIF26B was correlated with tumor size, positive LNM or distant metastases and poor prognosis.

Article Title: LncRNA PCAT1 and its genetic variant rs1902432 are associated with prostate cancer risk
Article Snippet: Total RNA was extracted from DU145 PCa cells using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's instructions. .. The mRNA of three pairs of DU145 cells transfected with PCAT1 overexpression vector or corresponding NC vector was profiled with Arraystar Human Gene Expression Array. ..

Article Title: SP-1-activated LINC01016 overexpression promotes gastric cancer invasion and metastasis through inhibiting EIF4A3-mediated MMP9 mRNA decay
Article Snippet: .. First, differential gene expression analysis of lncRNAs was performed between five cases of gastric cancers with LNM and another five cases without LNM using the Human Gene Expression Microarray (Human 8×60 K LncRNA Microarray v2.0; Arraystar, Rockville, USA). ..

Article Title: SP-1-activated LINC01016 overexpression promotes gastric cancer invasion and metastasis through inhibiting EIF4A3-mediated MMP9 mRNA decay.
Article Snippet: .. RESULTS LINC01016 is upregulated in GC with lymph node metastasis First, differential gene expression analysis of lncRNAs was performed between five cases of gastric cancers with LNM and another five cases without LNM using the Human Gene Expression Microarray (Human 8×60 K LncRNA Microarray v2.0; Arraystar, Rockville, USA). ..

Article Title: LncRNA PCAT1 and its genetic variant rs1902432 are associated with prostate cancer risk
Article Snippet: .. Arraystar Human Gene Expression Array was conducted to assess the genome-wide profiling of gene expression from PCa cell DU145 transfected with PCAT1 overexpression vector or NC vector. ..

Article Title: Long noncoding RNA lnc-LEMGC combines with DNA-PKcs to suppress gastric cancer metastasis.
Article Snippet: Long non-coding RNAs (lncRNAs) play important roles in cancer development and progression; however, their contributions to gastric cancer metastasis remain largely unknown.. By lncRNA microarray screening, our study showed that 453 lncRNAs are dysregulated in gastric cancer tissues with or without lymph node metastasis, of which lnc-LEMGC ranks as one of the most significantly downregulated lncRNAs.. Lnc-LEMGC inhibited cell migration and invasion both in vitro and in vivo, by combining with protein DNA-PKcs.

Article Title: PIN1P1 is activated by CREB1 and promotes gastric cancer progression via interacting with YBX1 and upregulating PIN1.
Article Snippet: .. Differential lncRNA screening was performed using the Human Gene Expression Microarray (Human 8 × 60 K LncRNA Microarray v2.0; Arraystar). ..

Microarray:

Article Title: KIF26B, a novel oncogene, promotes proliferation and metastasis by activating the VEGF pathway in gastric cancer.
Article Snippet: Tumor metastasis is the main reason of cancer-related death for gastric cancer (GC) patients and gene expression microarray data indicate that kinesin family member 26B (KIF26B) is one of the most upregulated genes in metastatic GC samples.. Specifically, KIF26B expression was upregulated in a stepwise manner from non-tumorous gastric mucosa, primary GC tissues without metastasis, via primary GC tissues with metastasis, to secondary lymph node metastatic (LNM) foci.. Increased expression of KIF26B was correlated with tumor size, positive LNM or distant metastases and poor prognosis.

Article Title: SP-1-activated LINC01016 overexpression promotes gastric cancer invasion and metastasis through inhibiting EIF4A3-mediated MMP9 mRNA decay
Article Snippet: .. First, differential gene expression analysis of lncRNAs was performed between five cases of gastric cancers with LNM and another five cases without LNM using the Human Gene Expression Microarray (Human 8×60 K LncRNA Microarray v2.0; Arraystar, Rockville, USA). ..

Article Title: SP-1-activated LINC01016 overexpression promotes gastric cancer invasion and metastasis through inhibiting EIF4A3-mediated MMP9 mRNA decay.
Article Snippet: .. RESULTS LINC01016 is upregulated in GC with lymph node metastasis First, differential gene expression analysis of lncRNAs was performed between five cases of gastric cancers with LNM and another five cases without LNM using the Human Gene Expression Microarray (Human 8×60 K LncRNA Microarray v2.0; Arraystar, Rockville, USA). ..

Article Title: Long noncoding RNA lnc-LEMGC combines with DNA-PKcs to suppress gastric cancer metastasis.
Article Snippet: Long non-coding RNAs (lncRNAs) play important roles in cancer development and progression; however, their contributions to gastric cancer metastasis remain largely unknown.. By lncRNA microarray screening, our study showed that 453 lncRNAs are dysregulated in gastric cancer tissues with or without lymph node metastasis, of which lnc-LEMGC ranks as one of the most significantly downregulated lncRNAs.. Lnc-LEMGC inhibited cell migration and invasion both in vitro and in vivo, by combining with protein DNA-PKcs.

Article Title: PIN1P1 is activated by CREB1 and promotes gastric cancer progression via interacting with YBX1 and upregulating PIN1.
Article Snippet: .. Differential lncRNA screening was performed using the Human Gene Expression Microarray (Human 8 × 60 K LncRNA Microarray v2.0; Arraystar). ..

Transfection:

Article Title: LncRNA PCAT1 and its genetic variant rs1902432 are associated with prostate cancer risk
Article Snippet: Total RNA was extracted from DU145 PCa cells using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's instructions. .. The mRNA of three pairs of DU145 cells transfected with PCAT1 overexpression vector or corresponding NC vector was profiled with Arraystar Human Gene Expression Array. ..

Article Title: LncRNA PCAT1 and its genetic variant rs1902432 are associated with prostate cancer risk
Article Snippet: .. Arraystar Human Gene Expression Array was conducted to assess the genome-wide profiling of gene expression from PCa cell DU145 transfected with PCAT1 overexpression vector or NC vector. ..

Over Expression:

Article Title: LncRNA PCAT1 and its genetic variant rs1902432 are associated with prostate cancer risk
Article Snippet: Total RNA was extracted from DU145 PCa cells using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's instructions. .. The mRNA of three pairs of DU145 cells transfected with PCAT1 overexpression vector or corresponding NC vector was profiled with Arraystar Human Gene Expression Array. ..

Article Title: LncRNA PCAT1 and its genetic variant rs1902432 are associated with prostate cancer risk
Article Snippet: .. Arraystar Human Gene Expression Array was conducted to assess the genome-wide profiling of gene expression from PCa cell DU145 transfected with PCAT1 overexpression vector or NC vector. ..

Plasmid Preparation:

Article Title: LncRNA PCAT1 and its genetic variant rs1902432 are associated with prostate cancer risk
Article Snippet: Total RNA was extracted from DU145 PCa cells using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's instructions. .. The mRNA of three pairs of DU145 cells transfected with PCAT1 overexpression vector or corresponding NC vector was profiled with Arraystar Human Gene Expression Array. ..

Article Title: LncRNA PCAT1 and its genetic variant rs1902432 are associated with prostate cancer risk
Article Snippet: .. Arraystar Human Gene Expression Array was conducted to assess the genome-wide profiling of gene expression from PCa cell DU145 transfected with PCAT1 overexpression vector or NC vector. ..

Genome Wide:

Article Title: LncRNA PCAT1 and its genetic variant rs1902432 are associated with prostate cancer risk
Article Snippet: .. Arraystar Human Gene Expression Array was conducted to assess the genome-wide profiling of gene expression from PCa cell DU145 transfected with PCAT1 overexpression vector or NC vector. ..



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NAC61 expression analysis. (A) NAC61 expression behavior in grapevine organs throughout development (bar plot) and compared in the heatmap (logarithmic value) with that of NAC60 and NAC33. The data were retrieved from the atlas transcriptomic dataset of cv. ‘Corvina’ ( Fasoli et al ., 2012 ). Each value represents the mean ±SD of three biological replicates. (B) Correlation between NAC61 expression level and sugar content in grape berries sampled from fruit set to maturity in cv. ‘Cabernet Sauvignon’ and cv. ‘Pinot noir’ ( Fasoli et al ., 2018 ). The black line represents the trend of the averaged values of the two varieties. The R 2 values shown correspond to the fitting of different polynomial regressions to each corresponding group of samples (orange for cv. ‘Cabernet Sauvignon’ samples, blue for cv. ‘Pinot noir’ samples, and black for the entire set of samples). (C) Correlation between NAC61 expression level and sugar content in grape berries sampled during post-harvest dehydration in six different varieties ( Zenoni et al ., 2016 ). (D) Correlation between NAC61 expression level and berry weight loss in cv. ‘Corvina’ berries sampled during traditional long and forced short post-harvest dehydration processes ( Zenoni et al ., 2020 ). Expression values were determined by <t>microarray</t> analysis and each value represents the mean ±SD from three biological replicates. (E) NAC61 GCNs based on berry, leaf, and tissue-independent (TI) datasets. Left, Venn diagram showing exclusive and shared genes based on the three datasets; right, three-dimensional plot of co-expressed genes in which NAC, WRKY, and ZIP family members already described as having involvement in berry ripening and/or stress responses are indicated.
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Summary of apoptosis pathways in human and Oncopig cells. Summarized apoptotic pathways altered by gemcitabine treatment in Oncopig BCCL and 5637 cells evaluated by <t>microarray.</t> There were multiple possible cellular pathways involved in apoptosis induction, such as: TP53INP1/P53/BCL/BAX/CASPASE mitochondrial intrinsical pathway; TP53INP1/TP73 activation; FAS/RB1/GADD45B/CASPASE pathway and cell rounding up by RND1 and/or ZMYM6.
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Image Search Results


NAC61 expression analysis. (A) NAC61 expression behavior in grapevine organs throughout development (bar plot) and compared in the heatmap (logarithmic value) with that of NAC60 and NAC33. The data were retrieved from the atlas transcriptomic dataset of cv. ‘Corvina’ ( Fasoli et al ., 2012 ). Each value represents the mean ±SD of three biological replicates. (B) Correlation between NAC61 expression level and sugar content in grape berries sampled from fruit set to maturity in cv. ‘Cabernet Sauvignon’ and cv. ‘Pinot noir’ ( Fasoli et al ., 2018 ). The black line represents the trend of the averaged values of the two varieties. The R 2 values shown correspond to the fitting of different polynomial regressions to each corresponding group of samples (orange for cv. ‘Cabernet Sauvignon’ samples, blue for cv. ‘Pinot noir’ samples, and black for the entire set of samples). (C) Correlation between NAC61 expression level and sugar content in grape berries sampled during post-harvest dehydration in six different varieties ( Zenoni et al ., 2016 ). (D) Correlation between NAC61 expression level and berry weight loss in cv. ‘Corvina’ berries sampled during traditional long and forced short post-harvest dehydration processes ( Zenoni et al ., 2020 ). Expression values were determined by microarray analysis and each value represents the mean ±SD from three biological replicates. (E) NAC61 GCNs based on berry, leaf, and tissue-independent (TI) datasets. Left, Venn diagram showing exclusive and shared genes based on the three datasets; right, three-dimensional plot of co-expressed genes in which NAC, WRKY, and ZIP family members already described as having involvement in berry ripening and/or stress responses are indicated.

Journal: Journal of Experimental Botany

Article Title: NAC61 regulates late- and post-ripening osmotic, oxidative, and biotic stress responses in grapevine

doi: 10.1093/jxb/erad507

Figure Lengend Snippet: NAC61 expression analysis. (A) NAC61 expression behavior in grapevine organs throughout development (bar plot) and compared in the heatmap (logarithmic value) with that of NAC60 and NAC33. The data were retrieved from the atlas transcriptomic dataset of cv. ‘Corvina’ ( Fasoli et al ., 2012 ). Each value represents the mean ±SD of three biological replicates. (B) Correlation between NAC61 expression level and sugar content in grape berries sampled from fruit set to maturity in cv. ‘Cabernet Sauvignon’ and cv. ‘Pinot noir’ ( Fasoli et al ., 2018 ). The black line represents the trend of the averaged values of the two varieties. The R 2 values shown correspond to the fitting of different polynomial regressions to each corresponding group of samples (orange for cv. ‘Cabernet Sauvignon’ samples, blue for cv. ‘Pinot noir’ samples, and black for the entire set of samples). (C) Correlation between NAC61 expression level and sugar content in grape berries sampled during post-harvest dehydration in six different varieties ( Zenoni et al ., 2016 ). (D) Correlation between NAC61 expression level and berry weight loss in cv. ‘Corvina’ berries sampled during traditional long and forced short post-harvest dehydration processes ( Zenoni et al ., 2020 ). Expression values were determined by microarray analysis and each value represents the mean ±SD from three biological replicates. (E) NAC61 GCNs based on berry, leaf, and tissue-independent (TI) datasets. Left, Venn diagram showing exclusive and shared genes based on the three datasets; right, three-dimensional plot of co-expressed genes in which NAC, WRKY, and ZIP family members already described as having involvement in berry ripening and/or stress responses are indicated.

Article Snippet: The cDNA synthesis, labelling, hybridization, and washing steps were performed according to the Agilent Microarray-Based Gene Expression Analysis Guide ( https://www.agilent.com/cs/library/usermanuals/Public/G4140-90040_GeneExpression_OneColor_6.9.pdf ).

Techniques: Expressing, Microarray

Summary of apoptosis pathways in human and Oncopig cells. Summarized apoptotic pathways altered by gemcitabine treatment in Oncopig BCCL and 5637 cells evaluated by microarray. There were multiple possible cellular pathways involved in apoptosis induction, such as: TP53INP1/P53/BCL/BAX/CASPASE mitochondrial intrinsical pathway; TP53INP1/TP73 activation; FAS/RB1/GADD45B/CASPASE pathway and cell rounding up by RND1 and/or ZMYM6.

Journal: Frontiers in Oncology

Article Title: Oncopig bladder cancer cells recapitulate human bladder cancer treatment responses in vitro

doi: 10.3389/fonc.2024.1323422

Figure Lengend Snippet: Summary of apoptosis pathways in human and Oncopig cells. Summarized apoptotic pathways altered by gemcitabine treatment in Oncopig BCCL and 5637 cells evaluated by microarray. There were multiple possible cellular pathways involved in apoptosis induction, such as: TP53INP1/P53/BCL/BAX/CASPASE mitochondrial intrinsical pathway; TP53INP1/TP73 activation; FAS/RB1/GADD45B/CASPASE pathway and cell rounding up by RND1 and/or ZMYM6.

Article Snippet: To obtain the gene transcription panel of treated and untreated human and Oncopig cells, the Two-Color Microarray-Based Gene Expression Analysis microarrays (Agilent Technologies Inc, Santa Clara, CA, USA) were used according to the manufacturer’s instructions.

Techniques: Microarray, Activation Assay