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Arraystar inc rat circrna array
Validation of <t>circRNA</t> and mRNA expression. A, The relative expression levels of selected circRNAs, as detected by RT‐qPCR. B, The relative expression levels of selected mRNAs, as detected by RT‐qPCR. β‐actin was used as a housekeeping gene for normalizing changes in specific gene expression. * P < .05 and ** P < .01 vs control group, n = 5 per group. RT‐PCR, real‐time quantitative polymerase chain reaction
Rat Circrna Array, 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
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1) Product Images from "Identification of circRNA and mRNA expression profiles and functional networks of vascular tissue in lipopolysaccharide‐induced sepsis"

Article Title: Identification of circRNA and mRNA expression profiles and functional networks of vascular tissue in lipopolysaccharide‐induced sepsis

Journal: Journal of Cellular and Molecular Medicine

doi: 10.1111/jcmm.15424

Validation of circRNA and mRNA expression. A, The relative expression levels of selected circRNAs, as detected by RT‐qPCR. B, The relative expression levels of selected mRNAs, as detected by RT‐qPCR. β‐actin was used as a housekeeping gene for normalizing changes in specific gene expression. * P < .05 and ** P < .01 vs control group, n = 5 per group. RT‐PCR, real‐time quantitative polymerase chain reaction
Figure Legend Snippet: Validation of circRNA and mRNA expression. A, The relative expression levels of selected circRNAs, as detected by RT‐qPCR. B, The relative expression levels of selected mRNAs, as detected by RT‐qPCR. β‐actin was used as a housekeeping gene for normalizing changes in specific gene expression. * P < .05 and ** P < .01 vs control group, n = 5 per group. RT‐PCR, real‐time quantitative polymerase chain reaction

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

Related Articles

Labeling:

Article Title: Therapeutic Target MicroRNA Identification Based on Circular RNA Expression Signature After Intracerebral Hemorrhage.
Article Snippet: Intracerebral hemorrhage (ICH) is a devastating stroke subtype with grave neurological outcome [1].. A specific therapeutic modality for ICH does not exist so far and diverse clinical trials with hemostatic agent, platelet transfusion, surgical hematoma evacuation, and blood pressure lowering have failed to improve functional outcome after ICH [2].. Thus, it is necessary to develop novel therapeutic strategy based on thorough understanding of neuronal injury mechanism following ICH [2].

Microarray:

Article Title: Therapeutic Target MicroRNA Identification Based on Circular RNA Expression Signature After Intracerebral Hemorrhage.
Article Snippet: Intracerebral hemorrhage (ICH) is a devastating stroke subtype with grave neurological outcome [1].. A specific therapeutic modality for ICH does not exist so far and diverse clinical trials with hemostatic agent, platelet transfusion, surgical hematoma evacuation, and blood pressure lowering have failed to improve functional outcome after ICH [2].. Thus, it is necessary to develop novel therapeutic strategy based on thorough understanding of neuronal injury mechanism following ICH [2].

Expressing:

Article Title: CircMAP3K5 promotes cardiomyocyte apoptosis in diabetic cardiomyopathy by regulating miR ‐22‐3p/ DAPK2 Axis
Article Snippet: .. To investigate the circRNA expression profile of DCM, we have applied the Arraystar Rat circRNA Array analysis of specimen from three DCM samples and three normal controls. .. A total of 14139 circRNAs were detected by Arraystar Rat circRNA Microarray.

Article Title: CircMAP3K5 promotes cardiomyocyte apoptosis in diabetic cardiomyopathy by regulating miR-22-3p/DAPK2 Axis.
Article Snippet: .. To investigate the circRNA expression profile of DCM, we have applied the Arraystar Rat circRNA Array analysis of specimen from three DCM samples and three normal controls. .. A total of 14139 circRNAs were detected by Arraystar Rat circRNA Microarray.

other:

Article Title: CircMAP3K5 promotes cardiomyocyte apoptosis in diabetic cardiomyopathy by regulating miR-22-3p/DAPK2 Axis.
Article Snippet: These circRNAs were amplified and transcribed into fluorescent cRNA using a random primer method (Arraystar Super RNA Labeling Kit; Arraystar). labeled cRNAs that were hybridized to Arraystar Rat circRNA Array V2.0 (8 15 K) with a total of 14 145 circRNA probes on the chip.

Article Title: CircMAP3K5 promotes cardiomyocyte apoptosis in diabetic cardiomyopathy by regulating miR ‐22‐3p/ DAPK2 Axis
Article Snippet: These circRNAs were amplified and transcribed into fluorescent cRNA using a random primer method (Arraystar Super RNA Labeling Kit; Arraystar). labeled cRNAs that were hybridized to Arraystar Rat circRNA Array V2.0 (8 × 15 K) with a total of 14 145 circRNA probes on the chip.

Article Title: Circular RNA expression profile and functional analysis of circUvrag in light-induced photoreceptor degeneration.
Article Snippet: Funding information National Natrual Science Foundation of China, Grant/Award Numbers: 81570855, 81790641 Abstract Background: Circular RNAs (circRNAs) are implicated in retinal pathophysiology; however, their expression profiles and functions in photoreceptor apoptosis are largely unknown.. We explored circRNA-expression profiles and circUvrag (host gene: Uvrag, ultraviolet radiation resistance associated gene) function in light-induced photoreceptor apoptosis.. Methods: Sprague–Dawley rats and 661 W photoreceptor cells were exposed to blue light to establish light-induced photoreceptor degeneration.



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Differentially expressed <t>circRNAs</t> in MS patients versus HCs, circRNA array analysis. ( A ) Volcano plots, used to visualize up- and downregulated genes across MS samples as compared to HCs. The red (up) and green (down) dots in the plot represent the significative differentially expressed circRNAs. ( B ) Clustered heatmap of the differentially expressed circRNAs showing the relationships among the expression levels of samples. Upregulation is shown in red, and downregulation is in green. ( C ) Table showing the list of circRNAs differentially expressed, depicting the top 7 upregulated and 10 downregulated.
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Differentially expressed <t>circRNAs</t> in MS patients versus HCs, circRNA array analysis. ( A ) Volcano plots, used to visualize up- and downregulated genes across MS samples as compared to HCs. The red (up) and green (down) dots in the plot represent the significative differentially expressed circRNAs. ( B ) Clustered heatmap of the differentially expressed circRNAs showing the relationships among the expression levels of samples. Upregulation is shown in red, and downregulation is in green. ( C ) Table showing the list of circRNAs differentially expressed, depicting the top 7 upregulated and 10 downregulated.
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Differentially expressed <t>circRNAs</t> in MS patients versus HCs, circRNA array analysis. ( A ) Volcano plots, used to visualize up- and downregulated genes across MS samples as compared to HCs. The red (up) and green (down) dots in the plot represent the significative differentially expressed circRNAs. ( B ) Clustered heatmap of the differentially expressed circRNAs showing the relationships among the expression levels of samples. Upregulation is shown in red, and downregulation is in green. ( C ) Table showing the list of circRNAs differentially expressed, depicting the top 7 upregulated and 10 downregulated.
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Circular RNAs are deregulated in human abdominal aortic aneurysm (A) Volcano plot depicting downregulated (51, blue) and upregulated (40, red). Circular RNAs <t>(circRNAs)</t> in human elective human abdominal aortic aneurysm (eAAA, n = 11) vs . control (CTRL, n = 6) aorta specimens, as resulted by array experiments. Log2 fold change and -log10 p value are plotted on the x and y axes, respectively. IDs of circRNAs meant for a first round of validation are highlighted. Statistics: unpaired t test; p values <0.05 are considered significant. (B) Pie chart illustrating the proportion of exonic (89.8%), intronic (5.7%), sense overlapping (3.4%), and antisense (1.1%) array-identified differentially expressed circRNAs. Absolute numbers are further indicated for each group. (C) Real-time quantitative PCR (qPCR) validation of hsa_circ_0005660 (c NFIX ), hsa_circ_0003641 (c ATM ), hsa_circ0042103 (c MYOCD ), hsa_circ003218 (c BMPR2 ), hsa_circ0004771 (c NRIP1 ), and hsa_circ0005615 (c NFATC3 ) differential expression in human eAAA (N = 8) and CTRL (N = 4) aortas. 2 –ddCT was calculated by normalizing on RPLPO . Data are represented as mean ± SEM. Statistics: unpaired t test; p values <0.05 are considered significant. NS, not significant; eAAA, elective AAA.
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Circular RNAs are deregulated in human abdominal aortic aneurysm (A) Volcano plot depicting downregulated (51, blue) and upregulated (40, red). Circular RNAs <t>(circRNAs)</t> in human elective human abdominal aortic aneurysm (eAAA, n = 11) vs . control (CTRL, n = 6) aorta specimens, as resulted by array experiments. Log2 fold change and -log10 p value are plotted on the x and y axes, respectively. IDs of circRNAs meant for a first round of validation are highlighted. Statistics: unpaired t test; p values <0.05 are considered significant. (B) Pie chart illustrating the proportion of exonic (89.8%), intronic (5.7%), sense overlapping (3.4%), and antisense (1.1%) array-identified differentially expressed circRNAs. Absolute numbers are further indicated for each group. (C) Real-time quantitative PCR (qPCR) validation of hsa_circ_0005660 (c NFIX ), hsa_circ_0003641 (c ATM ), hsa_circ0042103 (c MYOCD ), hsa_circ003218 (c BMPR2 ), hsa_circ0004771 (c NRIP1 ), and hsa_circ0005615 (c NFATC3 ) differential expression in human eAAA (N = 8) and CTRL (N = 4) aortas. 2 –ddCT was calculated by normalizing on RPLPO . Data are represented as mean ± SEM. Statistics: unpaired t test; p values <0.05 are considered significant. NS, not significant; eAAA, elective AAA.
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Image Search Results


Differentially expressed circRNAs in MS patients versus HCs, circRNA array analysis. ( A ) Volcano plots, used to visualize up- and downregulated genes across MS samples as compared to HCs. The red (up) and green (down) dots in the plot represent the significative differentially expressed circRNAs. ( B ) Clustered heatmap of the differentially expressed circRNAs showing the relationships among the expression levels of samples. Upregulation is shown in red, and downregulation is in green. ( C ) Table showing the list of circRNAs differentially expressed, depicting the top 7 upregulated and 10 downregulated.

Journal: Cells

Article Title: Identification of hsa_circ_0018905 as a New Potential Biomarker for Multiple Sclerosis

doi: 10.3390/cells13191668

Figure Lengend Snippet: Differentially expressed circRNAs in MS patients versus HCs, circRNA array analysis. ( A ) Volcano plots, used to visualize up- and downregulated genes across MS samples as compared to HCs. The red (up) and green (down) dots in the plot represent the significative differentially expressed circRNAs. ( B ) Clustered heatmap of the differentially expressed circRNAs showing the relationships among the expression levels of samples. Upregulation is shown in red, and downregulation is in green. ( C ) Table showing the list of circRNAs differentially expressed, depicting the top 7 upregulated and 10 downregulated.

Article Snippet: The Arraystar circRNAs Array was designed to identify 13,617 circRNAs, which were analyzed using the Agilent Feature Extraction software.

Techniques: Expressing

Characteristics of the circRNAs identified in PBMCs of MS patients versus HCs. ( A ) Distribution of significantly upregulated circRNAs according to the chromosomal location. ( B ) Class distribution of upregulated circRNAs based on the genomic origins. ( C ) Distribution of significantly downregulated circRNAs according to the chromosomal location. ( D ) Class distribution of downregulated circRNAs based on the genomic origins.

Journal: Cells

Article Title: Identification of hsa_circ_0018905 as a New Potential Biomarker for Multiple Sclerosis

doi: 10.3390/cells13191668

Figure Lengend Snippet: Characteristics of the circRNAs identified in PBMCs of MS patients versus HCs. ( A ) Distribution of significantly upregulated circRNAs according to the chromosomal location. ( B ) Class distribution of upregulated circRNAs based on the genomic origins. ( C ) Distribution of significantly downregulated circRNAs according to the chromosomal location. ( D ) Class distribution of downregulated circRNAs based on the genomic origins.

Article Snippet: The Arraystar circRNAs Array was designed to identify 13,617 circRNAs, which were analyzed using the Agilent Feature Extraction software.

Techniques:

Validation of the circRNAs identified in PBMCs of MS patients versus HCs. Expression levels in PBMCs of five upregulated and four downregulated circRNAs ( A ) and the corresponding cognate linear mRNAs ( B ) were measured by qPCR analysis. The levels of circRNAs and mRNAs were normalized to GAPDH mRNA levels. Data are the means and standard deviation (+SD) from at least three independent experiments. ** p < 0.01, *** p < 0.001.

Journal: Cells

Article Title: Identification of hsa_circ_0018905 as a New Potential Biomarker for Multiple Sclerosis

doi: 10.3390/cells13191668

Figure Lengend Snippet: Validation of the circRNAs identified in PBMCs of MS patients versus HCs. Expression levels in PBMCs of five upregulated and four downregulated circRNAs ( A ) and the corresponding cognate linear mRNAs ( B ) were measured by qPCR analysis. The levels of circRNAs and mRNAs were normalized to GAPDH mRNA levels. Data are the means and standard deviation (+SD) from at least three independent experiments. ** p < 0.01, *** p < 0.001.

Article Snippet: The Arraystar circRNAs Array was designed to identify 13,617 circRNAs, which were analyzed using the Agilent Feature Extraction software.

Techniques: Biomarker Discovery, Expressing, Standard Deviation

Validation of the circRNAs in serum of MS patients versus HCs. The levels in serum of five upregulated and four downregulated circRNAs ( A ) and the corresponding mRNAs ( B ) were measured by qPCR analysis. The levels of circRNAs and mRNAs were normalized to GAPDH mRNA levels. Data are the means and standard deviation (+SD) from at least three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001.

Journal: Cells

Article Title: Identification of hsa_circ_0018905 as a New Potential Biomarker for Multiple Sclerosis

doi: 10.3390/cells13191668

Figure Lengend Snippet: Validation of the circRNAs in serum of MS patients versus HCs. The levels in serum of five upregulated and four downregulated circRNAs ( A ) and the corresponding mRNAs ( B ) were measured by qPCR analysis. The levels of circRNAs and mRNAs were normalized to GAPDH mRNA levels. Data are the means and standard deviation (+SD) from at least three independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: The Arraystar circRNAs Array was designed to identify 13,617 circRNAs, which were analyzed using the Agilent Feature Extraction software.

Techniques: Biomarker Discovery, Standard Deviation

Identification of the miRNAs and RBP Targets. ( A ) Schematic representation of circRNAs with putative miRNA binding site (MRE) and RNA-binding protein binding site (RBP-bs). ( B , C ) Tables showing list of human circRNA identified from our studies and target miRNAs and interacting RNA-binding proteins as determined by analysis performed using miRanda and circInteractome, respectively.

Journal: Cells

Article Title: Identification of hsa_circ_0018905 as a New Potential Biomarker for Multiple Sclerosis

doi: 10.3390/cells13191668

Figure Lengend Snippet: Identification of the miRNAs and RBP Targets. ( A ) Schematic representation of circRNAs with putative miRNA binding site (MRE) and RNA-binding protein binding site (RBP-bs). ( B , C ) Tables showing list of human circRNA identified from our studies and target miRNAs and interacting RNA-binding proteins as determined by analysis performed using miRanda and circInteractome, respectively.

Article Snippet: The Arraystar circRNAs Array was designed to identify 13,617 circRNAs, which were analyzed using the Agilent Feature Extraction software.

Techniques: Binding Assay, RNA Binding Assay, Protein Binding

Network of circRNA-miRNA-mRNA for MS-associated genes. ( A ) Network of upregulated circRNAs and ( B ) downregulated circRNAs. CircRNAs are represented as red or green diamonds, miRNAs as red or green circles, and mRNAs as light red or light green rectangles. Red represents network generated from upregulated circRNAs and green from downregulated circRNAs.

Journal: Cells

Article Title: Identification of hsa_circ_0018905 as a New Potential Biomarker for Multiple Sclerosis

doi: 10.3390/cells13191668

Figure Lengend Snippet: Network of circRNA-miRNA-mRNA for MS-associated genes. ( A ) Network of upregulated circRNAs and ( B ) downregulated circRNAs. CircRNAs are represented as red or green diamonds, miRNAs as red or green circles, and mRNAs as light red or light green rectangles. Red represents network generated from upregulated circRNAs and green from downregulated circRNAs.

Article Snippet: The Arraystar circRNAs Array was designed to identify 13,617 circRNAs, which were analyzed using the Agilent Feature Extraction software.

Techniques: Generated

Validation of the circRNA expression in PBMCs and correlation with disease severity. ( A ) Expression levels in PBMCs of five upregulated and three downregulated circRNAs in MS with different disease severity measured by RT-qPCR analysis. The levels of circRNAs were normalized to GAPDH mRNA levels. ( B ) Receiver operating characteristic (ROC) curve of differentially expressed circRNAs in MS vs. HCs. Green line, hsa_circ_0003445 and blue line, hsa_circ_0018905. Data are represented as the means and standard deviation (+SD) from at least three independent experiments. ** p < 0.01, *** p < 0.001.

Journal: Cells

Article Title: Identification of hsa_circ_0018905 as a New Potential Biomarker for Multiple Sclerosis

doi: 10.3390/cells13191668

Figure Lengend Snippet: Validation of the circRNA expression in PBMCs and correlation with disease severity. ( A ) Expression levels in PBMCs of five upregulated and three downregulated circRNAs in MS with different disease severity measured by RT-qPCR analysis. The levels of circRNAs were normalized to GAPDH mRNA levels. ( B ) Receiver operating characteristic (ROC) curve of differentially expressed circRNAs in MS vs. HCs. Green line, hsa_circ_0003445 and blue line, hsa_circ_0018905. Data are represented as the means and standard deviation (+SD) from at least three independent experiments. ** p < 0.01, *** p < 0.001.

Article Snippet: The Arraystar circRNAs Array was designed to identify 13,617 circRNAs, which were analyzed using the Agilent Feature Extraction software.

Techniques: Biomarker Discovery, Expressing, Quantitative RT-PCR, Standard Deviation

Circular RNAs are deregulated in human abdominal aortic aneurysm (A) Volcano plot depicting downregulated (51, blue) and upregulated (40, red). Circular RNAs (circRNAs) in human elective human abdominal aortic aneurysm (eAAA, n = 11) vs . control (CTRL, n = 6) aorta specimens, as resulted by array experiments. Log2 fold change and -log10 p value are plotted on the x and y axes, respectively. IDs of circRNAs meant for a first round of validation are highlighted. Statistics: unpaired t test; p values <0.05 are considered significant. (B) Pie chart illustrating the proportion of exonic (89.8%), intronic (5.7%), sense overlapping (3.4%), and antisense (1.1%) array-identified differentially expressed circRNAs. Absolute numbers are further indicated for each group. (C) Real-time quantitative PCR (qPCR) validation of hsa_circ_0005660 (c NFIX ), hsa_circ_0003641 (c ATM ), hsa_circ0042103 (c MYOCD ), hsa_circ003218 (c BMPR2 ), hsa_circ0004771 (c NRIP1 ), and hsa_circ0005615 (c NFATC3 ) differential expression in human eAAA (N = 8) and CTRL (N = 4) aortas. 2 –ddCT was calculated by normalizing on RPLPO . Data are represented as mean ± SEM. Statistics: unpaired t test; p values <0.05 are considered significant. NS, not significant; eAAA, elective AAA.

Journal: Molecular Therapy. Nucleic Acids

Article Title: The circular RNA Ataxia Telangiectasia Mutated regulates oxidative stress in smooth muscle cells in expanding abdominal aortic aneurysms

doi: 10.1016/j.omtn.2023.08.017

Figure Lengend Snippet: Circular RNAs are deregulated in human abdominal aortic aneurysm (A) Volcano plot depicting downregulated (51, blue) and upregulated (40, red). Circular RNAs (circRNAs) in human elective human abdominal aortic aneurysm (eAAA, n = 11) vs . control (CTRL, n = 6) aorta specimens, as resulted by array experiments. Log2 fold change and -log10 p value are plotted on the x and y axes, respectively. IDs of circRNAs meant for a first round of validation are highlighted. Statistics: unpaired t test; p values <0.05 are considered significant. (B) Pie chart illustrating the proportion of exonic (89.8%), intronic (5.7%), sense overlapping (3.4%), and antisense (1.1%) array-identified differentially expressed circRNAs. Absolute numbers are further indicated for each group. (C) Real-time quantitative PCR (qPCR) validation of hsa_circ_0005660 (c NFIX ), hsa_circ_0003641 (c ATM ), hsa_circ0042103 (c MYOCD ), hsa_circ003218 (c BMPR2 ), hsa_circ0004771 (c NRIP1 ), and hsa_circ0005615 (c NFATC3 ) differential expression in human eAAA (N = 8) and CTRL (N = 4) aortas. 2 –ddCT was calculated by normalizing on RPLPO . Data are represented as mean ± SEM. Statistics: unpaired t test; p values <0.05 are considered significant. NS, not significant; eAAA, elective AAA.

Article Snippet: The resulting labeled cDNA was then purified and 1 μg was fragmented, heated, and subsequently hybridized with an 8 × 15k commercially available array chip displaying 13,617 human circRNAs (Arraystar, no. AS-S-CR-H-V2.0) for 17 h at 65°C in an Agilent Hybridization Oven.

Techniques: Control, Biomarker Discovery, Real-time Polymerase Chain Reaction, Quantitative Proteomics