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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+array/arraystar+human+circrna+microarray/pm39317084-68-24-28
    Average 90 stars, based on 1 article reviews
    arraystar mouse circrna array v2 - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Microarray:

    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.

    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.



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    Differentially expressed circRNAs and mRNAs in PGs of db/db mice comparing to db/m mice. ( A ) Volcano plots presenting differences in the expression of circRNAs between db/db and db/m mice. ( B ) Volcano plots presenting differences in the expression of mRNAs between db/db and db/m mice. ( C ) Heat map of top 30 upregulated and downregulated circRNAs with raw intensity higher than 500. ( D ) Heat map of top 30 upregulated and downregulated mRNAs with raw intensity higher than 500. Values plotted on the x- and y-axes represent the averaged normalized signal values of each group (log2-scaled). <t>CircRNA,</t> circular RNA; PGs, parotid glands; mRNA, massage RNA
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    Image Search Results


    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

    Differentially expressed circRNAs and mRNAs in PGs of db/db mice comparing to db/m mice. ( A ) Volcano plots presenting differences in the expression of circRNAs between db/db and db/m mice. ( B ) Volcano plots presenting differences in the expression of mRNAs between db/db and db/m mice. ( C ) Heat map of top 30 upregulated and downregulated circRNAs with raw intensity higher than 500. ( D ) Heat map of top 30 upregulated and downregulated mRNAs with raw intensity higher than 500. Values plotted on the x- and y-axes represent the averaged normalized signal values of each group (log2-scaled). CircRNA, circular RNA; PGs, parotid glands; mRNA, massage RNA

    Journal: BMC Genomics

    Article Title: Identification of circRNAs expression profiles and functional networks in parotid gland of type 2 diabetes mouse

    doi: 10.1186/s12864-024-10290-6

    Figure Lengend Snippet: Differentially expressed circRNAs and mRNAs in PGs of db/db mice comparing to db/m mice. ( A ) Volcano plots presenting differences in the expression of circRNAs between db/db and db/m mice. ( B ) Volcano plots presenting differences in the expression of mRNAs between db/db and db/m mice. ( C ) Heat map of top 30 upregulated and downregulated circRNAs with raw intensity higher than 500. ( D ) Heat map of top 30 upregulated and downregulated mRNAs with raw intensity higher than 500. Values plotted on the x- and y-axes represent the averaged normalized signal values of each group (log2-scaled). CircRNA, circular RNA; PGs, parotid glands; mRNA, massage RNA

    Article Snippet: The labelled cRNAs were hybridized onto the Arraystar Mouse circRNA Array (8 × 15 K; Arraystar).

    Techniques: Expressing

    Validation of DE circRNAs and mRNAs by qRT-PCR. ( A ) Expression of 5 selected upregulated circRNAs in db/db mice and db/m mice. ( B ) Expression of 9 selected downregulated circRNAs in db/db mice and db/m mice. ( C ) Expression of 10 selected upregulated mRNAs in db/db mice and db/m mice. ( D ) Expression of 10 selected downregulated mRNAs in db/db mice and db/m mice. * P < 0.05 and ** P < 0.01, versus db/m mice, n = 4. DE, differently expressed; circRNA, circular RNA; mRNA, massage RNA

    Journal: BMC Genomics

    Article Title: Identification of circRNAs expression profiles and functional networks in parotid gland of type 2 diabetes mouse

    doi: 10.1186/s12864-024-10290-6

    Figure Lengend Snippet: Validation of DE circRNAs and mRNAs by qRT-PCR. ( A ) Expression of 5 selected upregulated circRNAs in db/db mice and db/m mice. ( B ) Expression of 9 selected downregulated circRNAs in db/db mice and db/m mice. ( C ) Expression of 10 selected upregulated mRNAs in db/db mice and db/m mice. ( D ) Expression of 10 selected downregulated mRNAs in db/db mice and db/m mice. * P < 0.05 and ** P < 0.01, versus db/m mice, n = 4. DE, differently expressed; circRNA, circular RNA; mRNA, massage RNA

    Article Snippet: The labelled cRNAs were hybridized onto the Arraystar Mouse circRNA Array (8 × 15 K; Arraystar).

    Techniques: Quantitative RT-PCR, Expressing

    GO and KEGG pathway analysis based on CNC analysis of 7 selected circRNAs. ( A ) GO analysis of co-expressed mRNAs on cellular component (CC), biological process (BP), and molecular function (MF). ( B ) KEGG pathway analysis of co-expressed mRNAs of 7 selected circRNAs. GO, gene ontology; KEGG, kyoto encyclopedia of genes and genomes; CNC, coding–non-coding gene co-expression; mRNA, massage RNA; circRNA, circular RNA

    Journal: BMC Genomics

    Article Title: Identification of circRNAs expression profiles and functional networks in parotid gland of type 2 diabetes mouse

    doi: 10.1186/s12864-024-10290-6

    Figure Lengend Snippet: GO and KEGG pathway analysis based on CNC analysis of 7 selected circRNAs. ( A ) GO analysis of co-expressed mRNAs on cellular component (CC), biological process (BP), and molecular function (MF). ( B ) KEGG pathway analysis of co-expressed mRNAs of 7 selected circRNAs. GO, gene ontology; KEGG, kyoto encyclopedia of genes and genomes; CNC, coding–non-coding gene co-expression; mRNA, massage RNA; circRNA, circular RNA

    Article Snippet: The labelled cRNAs were hybridized onto the Arraystar Mouse circRNA Array (8 × 15 K; Arraystar).

    Techniques: Expressing

    Coding and non-coding co-expression network involving in PPAR signaling pathway, NF-kappa B signaling pathway, and cytokine-cytokine receptor interaction. Red nodes represent circRNAs; blue nodes represent mRNAs. Positive correlation is a solid line, negative correlation is a dashed line. PPAR, peroxisome proliferator-activated receptor; NF-kappa B, nuclear factor-kappa B; circRNA, circular RNA; mRNA, massage RNA

    Journal: BMC Genomics

    Article Title: Identification of circRNAs expression profiles and functional networks in parotid gland of type 2 diabetes mouse

    doi: 10.1186/s12864-024-10290-6

    Figure Lengend Snippet: Coding and non-coding co-expression network involving in PPAR signaling pathway, NF-kappa B signaling pathway, and cytokine-cytokine receptor interaction. Red nodes represent circRNAs; blue nodes represent mRNAs. Positive correlation is a solid line, negative correlation is a dashed line. PPAR, peroxisome proliferator-activated receptor; NF-kappa B, nuclear factor-kappa B; circRNA, circular RNA; mRNA, massage RNA

    Article Snippet: The labelled cRNAs were hybridized onto the Arraystar Mouse circRNA Array (8 × 15 K; Arraystar).

    Techniques: Expressing

    GO and KEGG pathway analysis based on ceRNA analysis of 7 selected circRNAs. ( A ) GO analysis of ceRNA function-related mRNAs on cellular component (CC), biological process (BP), and molecular function (MF). ( B ) KEGG pathway analysis of ceRNA function-related mRNAs. GO, gene ontology; KEGG, kyoto encyclopedia of genes and genomes; ceRNA, competing endogenous RNA; circRNA, circular RNA; mRNA, massage RNA

    Journal: BMC Genomics

    Article Title: Identification of circRNAs expression profiles and functional networks in parotid gland of type 2 diabetes mouse

    doi: 10.1186/s12864-024-10290-6

    Figure Lengend Snippet: GO and KEGG pathway analysis based on ceRNA analysis of 7 selected circRNAs. ( A ) GO analysis of ceRNA function-related mRNAs on cellular component (CC), biological process (BP), and molecular function (MF). ( B ) KEGG pathway analysis of ceRNA function-related mRNAs. GO, gene ontology; KEGG, kyoto encyclopedia of genes and genomes; ceRNA, competing endogenous RNA; circRNA, circular RNA; mRNA, massage RNA

    Article Snippet: The labelled cRNAs were hybridized onto the Arraystar Mouse circRNA Array (8 × 15 K; Arraystar).

    Techniques:

    CircRNA-miRNA-mRNA network involving in the regulation of actin cytoskeleton, leukocyte trans-endothelial migration, and PPAR signaling pathways. Green node represents upregulated circRNAs; yellow nodes represent downregulated circRNAs; red nodes represent miRNAs; blue nodes represent mRNAs. Purple lines with T-shape arrow represent directed relationships; orange lines without arrow represent undirected relationships. CircRNA, circular RNA; miRNA, microRNA; mRNA, massage RNA; PPAR, peroxisome proliferator-activated receptor

    Journal: BMC Genomics

    Article Title: Identification of circRNAs expression profiles and functional networks in parotid gland of type 2 diabetes mouse

    doi: 10.1186/s12864-024-10290-6

    Figure Lengend Snippet: CircRNA-miRNA-mRNA network involving in the regulation of actin cytoskeleton, leukocyte trans-endothelial migration, and PPAR signaling pathways. Green node represents upregulated circRNAs; yellow nodes represent downregulated circRNAs; red nodes represent miRNAs; blue nodes represent mRNAs. Purple lines with T-shape arrow represent directed relationships; orange lines without arrow represent undirected relationships. CircRNA, circular RNA; miRNA, microRNA; mRNA, massage RNA; PPAR, peroxisome proliferator-activated receptor

    Article Snippet: The labelled cRNAs were hybridized onto the Arraystar Mouse circRNA Array (8 × 15 K; Arraystar).

    Techniques: Migration

    The DE circRNAs, miRNAs, and mRNAs involved in the regulation of actin cytoskeleton signaling pathway

    Journal: BMC Genomics

    Article Title: Identification of circRNAs expression profiles and functional networks in parotid gland of type 2 diabetes mouse

    doi: 10.1186/s12864-024-10290-6

    Figure Lengend Snippet: The DE circRNAs, miRNAs, and mRNAs involved in the regulation of actin cytoskeleton signaling pathway

    Article Snippet: The labelled cRNAs were hybridized onto the Arraystar Mouse circRNA Array (8 × 15 K; Arraystar).

    Techniques:

    Primers for validated circRNAs

    Journal: BMC Genomics

    Article Title: Identification of circRNAs expression profiles and functional networks in parotid gland of type 2 diabetes mouse

    doi: 10.1186/s12864-024-10290-6

    Figure Lengend Snippet: Primers for validated circRNAs

    Article Snippet: The labelled cRNAs were hybridized onto the Arraystar Mouse circRNA Array (8 × 15 K; Arraystar).

    Techniques: