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KangChen Inc arraystar mouse circrna array v2
Arraystar Mouse Circrna Array V2, supplied by KangChen 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/arraystar+circrnas+array/arraystar+human+circrna+microarray/pm39317084-68-24-28
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Related Articles

Microarray:

Article Title: Downregulation of hsa_circ_0006220 and its correlation with clinicopathological factors in human breast cancer
Article Snippet: MDA-MB-231 cellswere cultured in DMEM (Gibco, Carlsbad, CA, USA), containing 10% fetal bovine serum (Hyclone, Logan, USA), and were maintained at 37 °C with 5% CO 2 in a humidified incubator. .. A total of 2,465 circRNAs in three breast cancer tissues and paired noncancerous tissues were analysed using an Arraystar Human circRNA Microarray (KangChen Bio-tech, Shanghai, China). .. A NanoDrop ND-1000 spectrophotometer (Thermo Scientific, Waltham, MA, USA) was used to quantify total RNA in each sample, and microarray hybridization was performed according to the Arraystar standard protocol.

Article Title: Skin wound repairing effects of adipose mesenchymal stem cells is promoted by the combined application of insulin-like growth factor 1: The key role of miR-21-5p-mediated signaling transduction.
Article Snippet: Mesenchymal stem cells (ADMSCs) have been applied to the treatment of skin injuries and the co-administration of cytokines can enhance the effects.. In the current study, the promoting effects of insulin-like growth factor 1 (IGF-1) on the skin wound healing effects of adipose-derived MSCs (ADMSCs) were assessed and the associated mechanism was explored by focusing on miR-21-5p mediated pathways.. ADMSCs were isolated from epididymis rats, and skin wounded rats were employed as the in vivo model for evaluating the effect of ADMCs on skin healing and secretion of cytokines.

Article Title: Downregulation of hsa_circ_0006220 and its correlation with clinicopathological factors in human breast cancer
Article Snippet: MDA-MB-231 cellswere cultured in DMEM (Gibco, Carlsbad, CA, USA), containing 10% fetal bovine serum (Hyclone, Logan, USA), and were maintained at 37 °C with 5% CO 2 in a humidified incubator. .. CircRNA microarray A total of 2,465 circRNAs in three breast cancer tissues and paired noncancerous tissues were analysed using an Arraystar Human circRNA Microarray (KangChen Bio-tech, Shanghai, China). .. A NanoDrop ND-1000 spectrophotometer (Thermo Scientific, Waltham, MA, USA) was used to quantify total RNA in each sample, and microarray hybridization was performed according to the Arraystar standard protocol.

Article Title: The decreased expression of hsa_circ_0043278 and its relationship with clinicopathological features of breast cancer
Article Snippet: .. The Arraystar Human circRNA Microarray (KangChen Biotech, Shanghai, China), which covered 2465 human circRNAs, was used to identify the differential expression of circRNAs among three pairs of breast cancer tissues and paired noncancerous tissues. .. The total number of RNA samples was quantified by NanoDrop ND-1000 (Thermo, USA).

Article Title: Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect
Article Snippet: .. Arraystar circRNA Microarray Technology (KANGCHEN, Shanghai, China) was used to analyze the differential expression of circRNAs. .. Total RNA was extracted from the samples using TRIzol Reagent (Invitrogen, Carlsbad CA, USA), according to manufacturer's instructions.

Article Title: The decreased expression of hsa_circ_0043278 and its relationship with clinicopathological features of breast cancer
Article Snippet: .. Written informed consent was retrieved from all participants in the study. circRNA microarray The Arraystar Human circRNA Microarray (KangChen Biotech, Shanghai, China), which covered 2465 human circRNAs, was used to identify the differential expression of circRNAs among three pairs of breast cancer tissues and paired noncancerous tissues. .. The total number of RNA samples was quantified by NanoDrop ND-1000 (Thermo, USA).

Mouse Assay:

Article Title: Circular RNA cVIM promotes hepatic stellate cell activation in liver fibrosis via miR-122-5p/miR-9-5p-mediated TGF-β signaling cascade
Article Snippet: .. To examine liver circRNAs that were differentially expressed between CCl 4 -treated mice ( n = 3) and healthy control mice ( n = 3), we employed the Arraystar Mouse circRNA Array V2 (manufactured by KangChen Bio-tech in Shanghai, China). .. The measurement of total RNA from each sample was performed utilizing the NanoDrop ND-1000 spectrophotometer.

Control:

Article Title: Circular RNA cVIM promotes hepatic stellate cell activation in liver fibrosis via miR-122-5p/miR-9-5p-mediated TGF-β signaling cascade
Article Snippet: .. To examine liver circRNAs that were differentially expressed between CCl 4 -treated mice ( n = 3) and healthy control mice ( n = 3), we employed the Arraystar Mouse circRNA Array V2 (manufactured by KangChen Bio-tech in Shanghai, China). .. The measurement of total RNA from each sample was performed utilizing the NanoDrop ND-1000 spectrophotometer.

Quantitative Proteomics:

Article Title: The decreased expression of hsa_circ_0043278 and its relationship with clinicopathological features of breast cancer
Article Snippet: .. The Arraystar Human circRNA Microarray (KangChen Biotech, Shanghai, China), which covered 2465 human circRNAs, was used to identify the differential expression of circRNAs among three pairs of breast cancer tissues and paired noncancerous tissues. .. The total number of RNA samples was quantified by NanoDrop ND-1000 (Thermo, USA).

Article Title: Differential Expression of CircRNAs in Embryonic Heart Tissue Associated with Ventricular Septal Defect
Article Snippet: .. Arraystar circRNA Microarray Technology (KANGCHEN, Shanghai, China) was used to analyze the differential expression of circRNAs. .. Total RNA was extracted from the samples using TRIzol Reagent (Invitrogen, Carlsbad CA, USA), according to manufacturer's instructions.

Article Title: The decreased expression of hsa_circ_0043278 and its relationship with clinicopathological features of breast cancer
Article Snippet: .. Written informed consent was retrieved from all participants in the study. circRNA microarray The Arraystar Human circRNA Microarray (KangChen Biotech, Shanghai, China), which covered 2465 human circRNAs, was used to identify the differential expression of circRNAs among three pairs of breast cancer tissues and paired noncancerous tissues. .. The total number of RNA samples was quantified by NanoDrop ND-1000 (Thermo, USA).



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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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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