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arraystar mouse circrna array v2  (KangChen Inc)

 
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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/mouse+circrna/arraystar+human+circrna+microarray/pm39317084-68-24-28
    Average 90 stars, based on 1 article reviews
    arraystar mouse circrna array v2 - by Bioz Stars, 2026-10
    90/100 stars

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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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    HFD-modulated gut microbiota regulates the expression of circRNAs. A, The <t>circRNA</t> expression profiles of intestinal tumors from CTL, HFD, and HFD+Abx AOM/DSS model mice were compared via high-throughput circRNA microarray sequencing. B, Mmu_circ_017841, mmu_circ_006689, mmu_circ_32011, circ_38945, mmu_circ_19191, mmu_circ_41893, and mmu_circ_45525, which appeared simultaneously in the upregulated circRNAs of the HFD vs. CTL and HFD+Abx groups. C–E , RT-qPCR was used to verify the differential expression of target mmu_circRNAs (mmu_circ_38945, mmu_circ_32011, mmu_circ_19191, and mmu_circ_45525) in groups of mice generated via three different modeling methods. F, Sanger sequencing results for circ_38945 and circ_0126925. G, Divergent and convergent primers were used to amplify circ_0126925, gDNA, and cDNA with or without RNase treatment before RT-qPCR. H, FISH analysis of the subcellular localization of circ_0126925. I, The proportions of cells in which circ_0126925 was expressed in the nucleus and cytoplasm. J and K, RT-qPCR and ISH were used to detect the expression of circ_0126925 in cancer and adjacent tissues. L, KM curve of the overall survival rate of patients with different expression levels of circ_0126925. In C–E , J , and K , unpaired and paired t tests were used for statistical analyses. In K , the differences between the KM curves were tested for significance by the log-rank test. *, P < 0.05; **, P < 0.01; ***, P < 0.001. ns indicates no significant difference between the two indicated groups.
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    HFD-modulated gut microbiota regulates the expression of circRNAs. A, The <t>circRNA</t> expression profiles of intestinal tumors from CTL, HFD, and HFD+Abx AOM/DSS model mice were compared via high-throughput circRNA microarray sequencing. B, Mmu_circ_017841, mmu_circ_006689, mmu_circ_32011, circ_38945, mmu_circ_19191, mmu_circ_41893, and mmu_circ_45525, which appeared simultaneously in the upregulated circRNAs of the HFD vs. CTL and HFD+Abx groups. C–E , RT-qPCR was used to verify the differential expression of target mmu_circRNAs (mmu_circ_38945, mmu_circ_32011, mmu_circ_19191, and mmu_circ_45525) in groups of mice generated via three different modeling methods. F, Sanger sequencing results for circ_38945 and circ_0126925. G, Divergent and convergent primers were used to amplify circ_0126925, gDNA, and cDNA with or without RNase treatment before RT-qPCR. H, FISH analysis of the subcellular localization of circ_0126925. I, The proportions of cells in which circ_0126925 was expressed in the nucleus and cytoplasm. J and K, RT-qPCR and ISH were used to detect the expression of circ_0126925 in cancer and adjacent tissues. L, KM curve of the overall survival rate of patients with different expression levels of circ_0126925. In C–E , J , and K , unpaired and paired t tests were used for statistical analyses. In K , the differences between the KM curves were tested for significance by the log-rank test. *, P < 0.05; **, P < 0.01; ***, P < 0.001. ns indicates no significant difference between the two indicated groups.
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    HFD-modulated gut microbiota regulates the expression of circRNAs. A, The circRNA expression profiles of intestinal tumors from CTL, HFD, and HFD+Abx AOM/DSS model mice were compared via high-throughput circRNA microarray sequencing. B, Mmu_circ_017841, mmu_circ_006689, mmu_circ_32011, circ_38945, mmu_circ_19191, mmu_circ_41893, and mmu_circ_45525, which appeared simultaneously in the upregulated circRNAs of the HFD vs. CTL and HFD+Abx groups. C–E , RT-qPCR was used to verify the differential expression of target mmu_circRNAs (mmu_circ_38945, mmu_circ_32011, mmu_circ_19191, and mmu_circ_45525) in groups of mice generated via three different modeling methods. F, Sanger sequencing results for circ_38945 and circ_0126925. G, Divergent and convergent primers were used to amplify circ_0126925, gDNA, and cDNA with or without RNase treatment before RT-qPCR. H, FISH analysis of the subcellular localization of circ_0126925. I, The proportions of cells in which circ_0126925 was expressed in the nucleus and cytoplasm. J and K, RT-qPCR and ISH were used to detect the expression of circ_0126925 in cancer and adjacent tissues. L, KM curve of the overall survival rate of patients with different expression levels of circ_0126925. In C–E , J , and K , unpaired and paired t tests were used for statistical analyses. In K , the differences between the KM curves were tested for significance by the log-rank test. *, P < 0.05; **, P < 0.01; ***, P < 0.001. ns indicates no significant difference between the two indicated groups.

    Journal: Molecular Cancer Research

    Article Title: Gut Microbiota–Mediated hsa_circ_0126925 Targets BCAA Metabolic Enzyme BCAT2 to Exacerbate Colorectal Cancer Progression

    doi: 10.1158/1541-7786.MCR-24-0434

    Figure Lengend Snippet: HFD-modulated gut microbiota regulates the expression of circRNAs. A, The circRNA expression profiles of intestinal tumors from CTL, HFD, and HFD+Abx AOM/DSS model mice were compared via high-throughput circRNA microarray sequencing. B, Mmu_circ_017841, mmu_circ_006689, mmu_circ_32011, circ_38945, mmu_circ_19191, mmu_circ_41893, and mmu_circ_45525, which appeared simultaneously in the upregulated circRNAs of the HFD vs. CTL and HFD+Abx groups. C–E , RT-qPCR was used to verify the differential expression of target mmu_circRNAs (mmu_circ_38945, mmu_circ_32011, mmu_circ_19191, and mmu_circ_45525) in groups of mice generated via three different modeling methods. F, Sanger sequencing results for circ_38945 and circ_0126925. G, Divergent and convergent primers were used to amplify circ_0126925, gDNA, and cDNA with or without RNase treatment before RT-qPCR. H, FISH analysis of the subcellular localization of circ_0126925. I, The proportions of cells in which circ_0126925 was expressed in the nucleus and cytoplasm. J and K, RT-qPCR and ISH were used to detect the expression of circ_0126925 in cancer and adjacent tissues. L, KM curve of the overall survival rate of patients with different expression levels of circ_0126925. In C–E , J , and K , unpaired and paired t tests were used for statistical analyses. In K , the differences between the KM curves were tested for significance by the log-rank test. *, P < 0.05; **, P < 0.01; ***, P < 0.001. ns indicates no significant difference between the two indicated groups.

    Article Snippet: Then, the labeled circRNA was hybridized onto an Arraystar Mouse circRNA Array (8 × 15 K, Arraystar) and incubated in an Agilent Hybridization Incubator (Agilent) at 65°C for 17 hours.

    Techniques: Expressing, High Throughput Screening Assay, Microarray, Sequencing, Quantitative RT-PCR, Quantitative Proteomics, Generated