Review



strand specific transcriptome library preparation  (Novogene)

 
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 86

    Structured Review

    Novogene strand specific transcriptome library preparation
    Strand Specific Transcriptome Library Preparation, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transcriptomic+libraries/library+preparation+specific+strand+transcriptome/pmc12787643-361-0-7
    Average 86 stars, based on 1 article reviews
    strand specific transcriptome library preparation - by Bioz Stars, 2026-10
    86/100 stars

    Images

    Related Articles

    Construct:

    Article Title: The microbial tryptophan metabolite indole acts on the gastrointestinal tract to improve glucose homeostasis in a mouse model of diabetes by enhancing GLP-1 secretion and L cell differentiation.
    Article Snippet: RNA sequencing Purified total RNA samples were analysed using Nanodrop (A260/A280 >1.8, suggesting good RNA purity), and RNA integrity was checked using an Agilent Bioanalyzer RNA 6000 Nano assay (RNA integrity number [RIN] >7). .. Strand-specific mRNA (polyA) libraries were constructed at Novogene UK, and sequenced using an Illumina NovaSeq 6000 sequencing system with 5.8–7.9 billion bases per sample. .. Adapters were trimmed using Novogene’s bioinformatics pipeline, and alignments were performed using HISAT2 [18] and mouse genome GRCm38 Ensembl version 102.

    Sequencing:

    Article Title: The microbial tryptophan metabolite indole acts on the gastrointestinal tract to improve glucose homeostasis in a mouse model of diabetes by enhancing GLP-1 secretion and L cell differentiation.
    Article Snippet: RNA sequencing Purified total RNA samples were analysed using Nanodrop (A260/A280 >1.8, suggesting good RNA purity), and RNA integrity was checked using an Agilent Bioanalyzer RNA 6000 Nano assay (RNA integrity number [RIN] >7). .. Strand-specific mRNA (polyA) libraries were constructed at Novogene UK, and sequenced using an Illumina NovaSeq 6000 sequencing system with 5.8–7.9 billion bases per sample. .. Adapters were trimmed using Novogene’s bioinformatics pipeline, and alignments were performed using HISAT2 [18] and mouse genome GRCm38 Ensembl version 102.

    Article Title: Genotype‐Dependent Transcriptome Divergence Associated With Variation at vgll3 in Juvenile Gilthead Seabream ( Sparus aurata )
    Article Snippet: RNA quality and integrity were confirmed by electrophoresis in 1.5% agarose gels and spectrophotometric quantification (Nanodrop 2000, Thermo Fisher Scientific, Waltham, USA). .. The RNA samples were outsourced (Novogene, Europe, UK) for strand‐specific mRNA library preparation using poly‐A selection, followed by paired‐end sequencing (150‐bp reads) on the Illumina NovaSeq platforms. ..

    Article Title: Two LEAFY homologues regulate floral patterning and development without affecting flowering time in kiwifruit.
    Article Snippet: 14 For RNA-seq, the quantity and quality of RNA samples were checked using a Bioanalyzer 2100 15 (Agilent Technologies, USA) with the RIN score above 7. .. RNA was sent to Novogene (Hong 16 Kong) for directional strand-specific mRNA library preparation and NovaSeq 6000 PE150 17 sequencing. ..

    Article Title: Genotype-Dependent Transcriptome Divergence Associated With Variation at vgll3 in Juvenile Gilthead Seabream (Sparus aurata).
    Article Snippet: RNA quality and integrity were confirmed by electrophoresis in 1.5% agarose gels and spectrophotometric quantification (Nanodrop 2000, Thermo Fisher Scientific, Waltham, USA). .. The RNA samples were outsourced (Novogene, Europe, UK) for strand- specific mRNA library preparation using poly- A selection, followed by paired- end sequencing (150- bp reads) on the Illumina NovaSeq platforms. ..

    cDNA Synthesis:

    Article Title: Comparative Analysis of Insect Resistance in Transgenic Populus × euramericana cv. Neva Expressing Dual Bt Genes from Different Sources
    Article Snippet: RNA quality was verified via NanoDrop 2000 (Thermo Fisher Scientific, Waltham, MA, USA) and Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA), with an RNA integrity number (RIN) ≥ 7.0 required for library construction [ ]. .. Strand-specific transcriptome library preparation was performed by Novogene (Beijing, China) following their standard protocol for insect samples [ , ], which included mRNA enrichment, fragmentation, cDNA synthesis, end repair, adapter ligation, size selection, and PCR amplification. .. The qualified library was sequenced on an Illumina NovaSeq 6000 platform to generate paired-end reads [ ].

    Adapter Ligation:

    Article Title: Comparative Analysis of Insect Resistance in Transgenic Populus × euramericana cv. Neva Expressing Dual Bt Genes from Different Sources
    Article Snippet: RNA quality was verified via NanoDrop 2000 (Thermo Fisher Scientific, Waltham, MA, USA) and Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA), with an RNA integrity number (RIN) ≥ 7.0 required for library construction [ ]. .. Strand-specific transcriptome library preparation was performed by Novogene (Beijing, China) following their standard protocol for insect samples [ , ], which included mRNA enrichment, fragmentation, cDNA synthesis, end repair, adapter ligation, size selection, and PCR amplification. .. The qualified library was sequenced on an Illumina NovaSeq 6000 platform to generate paired-end reads [ ].

    Size Selection:

    Article Title: Comparative Analysis of Insect Resistance in Transgenic Populus × euramericana cv. Neva Expressing Dual Bt Genes from Different Sources
    Article Snippet: RNA quality was verified via NanoDrop 2000 (Thermo Fisher Scientific, Waltham, MA, USA) and Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA), with an RNA integrity number (RIN) ≥ 7.0 required for library construction [ ]. .. Strand-specific transcriptome library preparation was performed by Novogene (Beijing, China) following their standard protocol for insect samples [ , ], which included mRNA enrichment, fragmentation, cDNA synthesis, end repair, adapter ligation, size selection, and PCR amplification. .. The qualified library was sequenced on an Illumina NovaSeq 6000 platform to generate paired-end reads [ ].

    Polymerase Chain Reaction:

    Article Title: Comparative Analysis of Insect Resistance in Transgenic Populus × euramericana cv. Neva Expressing Dual Bt Genes from Different Sources
    Article Snippet: RNA quality was verified via NanoDrop 2000 (Thermo Fisher Scientific, Waltham, MA, USA) and Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA), with an RNA integrity number (RIN) ≥ 7.0 required for library construction [ ]. .. Strand-specific transcriptome library preparation was performed by Novogene (Beijing, China) following their standard protocol for insect samples [ , ], which included mRNA enrichment, fragmentation, cDNA synthesis, end repair, adapter ligation, size selection, and PCR amplification. .. The qualified library was sequenced on an Illumina NovaSeq 6000 platform to generate paired-end reads [ ].

    Amplification:

    Article Title: Comparative Analysis of Insect Resistance in Transgenic Populus × euramericana cv. Neva Expressing Dual Bt Genes from Different Sources
    Article Snippet: RNA quality was verified via NanoDrop 2000 (Thermo Fisher Scientific, Waltham, MA, USA) and Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA), with an RNA integrity number (RIN) ≥ 7.0 required for library construction [ ]. .. Strand-specific transcriptome library preparation was performed by Novogene (Beijing, China) following their standard protocol for insect samples [ , ], which included mRNA enrichment, fragmentation, cDNA synthesis, end repair, adapter ligation, size selection, and PCR amplification. .. The qualified library was sequenced on an Illumina NovaSeq 6000 platform to generate paired-end reads [ ].

    Selection:

    Article Title: Genotype‐Dependent Transcriptome Divergence Associated With Variation at vgll3 in Juvenile Gilthead Seabream ( Sparus aurata )
    Article Snippet: RNA quality and integrity were confirmed by electrophoresis in 1.5% agarose gels and spectrophotometric quantification (Nanodrop 2000, Thermo Fisher Scientific, Waltham, USA). .. The RNA samples were outsourced (Novogene, Europe, UK) for strand‐specific mRNA library preparation using poly‐A selection, followed by paired‐end sequencing (150‐bp reads) on the Illumina NovaSeq platforms. ..

    Article Title: Genotype-Dependent Transcriptome Divergence Associated With Variation at vgll3 in Juvenile Gilthead Seabream (Sparus aurata).
    Article Snippet: RNA quality and integrity were confirmed by electrophoresis in 1.5% agarose gels and spectrophotometric quantification (Nanodrop 2000, Thermo Fisher Scientific, Waltham, USA). .. The RNA samples were outsourced (Novogene, Europe, UK) for strand- specific mRNA library preparation using poly- A selection, followed by paired- end sequencing (150- bp reads) on the Illumina NovaSeq platforms. ..

    RNA Sequencing:

    Article Title: Hyperuricemia aggravates acute pancreatitis through CNR1-mediated inflammatory signaling and gut-pancreas axis dysregulation: a multi-omics and clinical study.
    Article Snippet: RNA quality was assessed using the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA) to ensure integrity and purity. .. Strand-specific RNA-seq libraries were prepared by Novogene Co., Ltd. (Beijing, China) following standard protocols. .. The clustering of indexcoded samples was performed on the cBot Cluster Generation System using the TruSeq PE Cluster Kit v3-cBot-HS (Illumina, CA, USA) according to the manufacturer's guidelines.

    Article Title: FACT depletion results in a temporal cascade of chromatin disruption preceding transcriptional collapse in stem cells
    Article Snippet: .. Purified steady-state RNA samples were used as an input for strand specific RNA-seq library builds using Novogene. .. Libraries were pooled and paired end sequencing was performed using Illumina Novaseq platform to a depth of ∼30 million reads.

    RNA sequencing:

    Article Title: Metabolic stress reveals widespread accumulation of cap-unmethylated RNAs
    Article Snippet: 300 ng poly(A)+ RNA was added to the beads in 200 μL RIP buffer with 0.1U/μL SUPERase·In (ThermoFisher, AM2696), and incubated at 4°C overnight with rotation. .. The RNA pellet was resuspended in 20 μL water and two biological replicates were subjected to strand-specific RNA-sequencing with Novogene. ..

    Purification:

    Article Title: FACT depletion results in a temporal cascade of chromatin disruption preceding transcriptional collapse in stem cells
    Article Snippet: .. Purified steady-state RNA samples were used as an input for strand specific RNA-seq library builds using Novogene. .. Libraries were pooled and paired end sequencing was performed using Illumina Novaseq platform to a depth of ∼30 million reads.



    Similar Products

    96
    Twist Bioscience whole transcriptome library preparation kit
    Whole Transcriptome Library Preparation Kit, supplied by Twist Bioscience, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transcriptomic+libraries/Twist+Library+Preparation+Kit%2C+Mechanical+Fragmentation/med_rxiv__64898__2026__06__23__26355479-54-16-15
    Average 96 stars, based on 1 article reviews
    whole transcriptome library preparation kit - by Bioz Stars, 2026-10
    96/100 stars
      Buy from Supplier

    98
    Complete Genomics Inc transcriptome library construction
    Changes in intestinal short chain fatty acids and spleen <t>transcriptome</t> in mice treated with SYD. (A) The boxplot of acetic acid abundance among three groups; (B) The boxplot of isobutyric acid abundance among three groups; (C) Differences in PISA scores among the three groups; (D) Differences in body weight among three groups of mice; (E) and (F) The difference in thickness between the left and right ears of mice among the three groups; (G) The correlation between short chain fatty acids and phenotype indicators in mice, yellow represents positive correlation, blue represents negative correlation, and darker colors indicate higher correlation coefficients; (H) The volcano plot of transcriptome between Psoriasis and SYD Treatment groups; (I) The heatmap of inflammation related genes among significant differentially expressed genes; (J) The dot plot of GO enrichment analysis of upregulated genes; (K) The GSEA analysis of the G protein-coupled receptor signaling pathway; (L) The analysis of CIBERSORT, which displayed the relative abundance of different cell subpopulations in three groups; (M) The box plot shows significant differences in the abundance of plasma, Treg, and Tfh cell subpopulations among the three groups.
    Transcriptome Library Construction, supplied by Complete Genomics Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transcriptomic+libraries/MGIEasy+Fast+RNA+Library+Prep+Set/pmc13132127-59-6-15
    Average 98 stars, based on 1 article reviews
    transcriptome library construction - by Bioz Stars, 2026-10
    98/100 stars
      Buy from Supplier

    86
    Novogene 104 transcriptome library preparation
    Changes in intestinal short chain fatty acids and spleen <t>transcriptome</t> in mice treated with SYD. (A) The boxplot of acetic acid abundance among three groups; (B) The boxplot of isobutyric acid abundance among three groups; (C) Differences in PISA scores among the three groups; (D) Differences in body weight among three groups of mice; (E) and (F) The difference in thickness between the left and right ears of mice among the three groups; (G) The correlation between short chain fatty acids and phenotype indicators in mice, yellow represents positive correlation, blue represents negative correlation, and darker colors indicate higher correlation coefficients; (H) The volcano plot of transcriptome between Psoriasis and SYD Treatment groups; (I) The heatmap of inflammation related genes among significant differentially expressed genes; (J) The dot plot of GO enrichment analysis of upregulated genes; (K) The GSEA analysis of the G protein-coupled receptor signaling pathway; (L) The analysis of CIBERSORT, which displayed the relative abundance of different cell subpopulations in three groups; (M) The box plot shows significant differences in the abundance of plasma, Treg, and Tfh cell subpopulations among the three groups.
    104 Transcriptome Library Preparation, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transcriptomic+libraries/104+library+preparation+transcriptome/10__1016_slash_j__hpj__2025__09__016-57-0-10
    Average 86 stars, based on 1 article reviews
    104 transcriptome library preparation - by Bioz Stars, 2026-10
    86/100 stars
      Buy from Supplier

    99
    Complete Genomics Inc sequencing stomics libraries
    Changes in intestinal short chain fatty acids and spleen <t>transcriptome</t> in mice treated with SYD. (A) The boxplot of acetic acid abundance among three groups; (B) The boxplot of isobutyric acid abundance among three groups; (C) Differences in PISA scores among the three groups; (D) Differences in body weight among three groups of mice; (E) and (F) The difference in thickness between the left and right ears of mice among the three groups; (G) The correlation between short chain fatty acids and phenotype indicators in mice, yellow represents positive correlation, blue represents negative correlation, and darker colors indicate higher correlation coefficients; (H) The volcano plot of transcriptome between Psoriasis and SYD Treatment groups; (I) The heatmap of inflammation related genes among significant differentially expressed genes; (J) The dot plot of GO enrichment analysis of upregulated genes; (K) The GSEA analysis of the G protein-coupled receptor signaling pathway; (L) The analysis of CIBERSORT, which displayed the relative abundance of different cell subpopulations in three groups; (M) The box plot shows significant differences in the abundance of plasma, Treg, and Tfh cell subpopulations among the three groups.
    Sequencing Stomics Libraries, supplied by Complete Genomics Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transcriptomic+libraries/Stereo-seq+Transcriptomics+Set+for+FFPE/pm41723140-256-4-5
    Average 99 stars, based on 1 article reviews
    sequencing stomics libraries - by Bioz Stars, 2026-10
    99/100 stars
      Buy from Supplier

    86
    Annoroad Gene Technology Co Ltd spatial transcriptome analysis stereo seq library preparation stereo seq library construction
    Changes in intestinal short chain fatty acids and spleen <t>transcriptome</t> in mice treated with SYD. (A) The boxplot of acetic acid abundance among three groups; (B) The boxplot of isobutyric acid abundance among three groups; (C) Differences in PISA scores among the three groups; (D) Differences in body weight among three groups of mice; (E) and (F) The difference in thickness between the left and right ears of mice among the three groups; (G) The correlation between short chain fatty acids and phenotype indicators in mice, yellow represents positive correlation, blue represents negative correlation, and darker colors indicate higher correlation coefficients; (H) The volcano plot of transcriptome between Psoriasis and SYD Treatment groups; (I) The heatmap of inflammation related genes among significant differentially expressed genes; (J) The dot plot of GO enrichment analysis of upregulated genes; (K) The GSEA analysis of the G protein-coupled receptor signaling pathway; (L) The analysis of CIBERSORT, which displayed the relative abundance of different cell subpopulations in three groups; (M) The box plot shows significant differences in the abundance of plasma, Treg, and Tfh cell subpopulations among the three groups.
    Spatial Transcriptome Analysis Stereo Seq Library Preparation Stereo Seq Library Construction, supplied by Annoroad Gene Technology Co Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transcriptomic+libraries/construction+library+scrna+seq/pm41715200-176-0-13
    Average 86 stars, based on 1 article reviews
    spatial transcriptome analysis stereo seq library preparation stereo seq library construction - by Bioz Stars, 2026-10
    86/100 stars
      Buy from Supplier

    86
    Novogene transcriptome sequencing library preparation
    Changes in intestinal short chain fatty acids and spleen <t>transcriptome</t> in mice treated with SYD. (A) The boxplot of acetic acid abundance among three groups; (B) The boxplot of isobutyric acid abundance among three groups; (C) Differences in PISA scores among the three groups; (D) Differences in body weight among three groups of mice; (E) and (F) The difference in thickness between the left and right ears of mice among the three groups; (G) The correlation between short chain fatty acids and phenotype indicators in mice, yellow represents positive correlation, blue represents negative correlation, and darker colors indicate higher correlation coefficients; (H) The volcano plot of transcriptome between Psoriasis and SYD Treatment groups; (I) The heatmap of inflammation related genes among significant differentially expressed genes; (J) The dot plot of GO enrichment analysis of upregulated genes; (K) The GSEA analysis of the G protein-coupled receptor signaling pathway; (L) The analysis of CIBERSORT, which displayed the relative abundance of different cell subpopulations in three groups; (M) The box plot shows significant differences in the abundance of plasma, Treg, and Tfh cell subpopulations among the three groups.
    Transcriptome Sequencing Library Preparation, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transcriptomic+libraries/library+preparation+sequencing+transcriptome/pm41747444-104-3-15
    Average 86 stars, based on 1 article reviews
    transcriptome sequencing library preparation - by Bioz Stars, 2026-10
    86/100 stars
      Buy from Supplier

    86
    Novogene whole retina transcriptome libraries
    Changes in intestinal short chain fatty acids and spleen <t>transcriptome</t> in mice treated with SYD. (A) The boxplot of acetic acid abundance among three groups; (B) The boxplot of isobutyric acid abundance among three groups; (C) Differences in PISA scores among the three groups; (D) Differences in body weight among three groups of mice; (E) and (F) The difference in thickness between the left and right ears of mice among the three groups; (G) The correlation between short chain fatty acids and phenotype indicators in mice, yellow represents positive correlation, blue represents negative correlation, and darker colors indicate higher correlation coefficients; (H) The volcano plot of transcriptome between Psoriasis and SYD Treatment groups; (I) The heatmap of inflammation related genes among significant differentially expressed genes; (J) The dot plot of GO enrichment analysis of upregulated genes; (K) The GSEA analysis of the G protein-coupled receptor signaling pathway; (L) The analysis of CIBERSORT, which displayed the relative abundance of different cell subpopulations in three groups; (M) The box plot shows significant differences in the abundance of plasma, Treg, and Tfh cell subpopulations among the three groups.
    Whole Retina Transcriptome Libraries, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transcriptomic+libraries/libraries+retina+transcriptome+whole/pm41671374-166-8-18
    Average 86 stars, based on 1 article reviews
    whole retina transcriptome libraries - by Bioz Stars, 2026-10
    86/100 stars
      Buy from Supplier

    99
    Illumina Inc rna sequencing transcriptome library
    a Schematic illustration of the <t>RNA-seq</t> and metabolomics analyses. b Gene cluster trend in different groups ( n = 3 mice). c GO enrichment analysis of genes in cluster 1. d GO enrichment analysis of genes in cluster 3. e GO enrichment analysis of genes in cluster 4. GO enrichment analysis was performed using a one-sided hypergeo metric test. Terms with a p < 0.05 were considered significantly enriched. f Heatmap o f the relative abundance of proinflammatory cytokines and purine metabolic genes in the three groups ( n = 3 mice). g PCA score plot of different groups subjected to metabolic analysis. h Pathway enrichment analysis of the DEMs enriched in ALI mice treated with ND@Monos (vs. the ALI group). Significance of enrichment was determined by a hypergeometric test with an FDR-corrected p -value ( q -value) threshold of 0.05. i , j Western blot analysis and quantification of IL-1β, P-creb and P-P65 levels ( n = 5 mice). Data are presented as mean ± SD. NC group indicates normal mice, and PBS indicates mice treated with vehicle. Statistical analysis was performed by one-way ANOVA with Tukey’s multiple comparison test. Source data are provided as a Source Data file.
    Rna Sequencing Transcriptome Library, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transcriptomic+libraries/TruSeq+RNA+Library+Prep/pmc12946169-402-1-16
    Average 99 stars, based on 1 article reviews
    rna sequencing transcriptome library - by Bioz Stars, 2026-10
    99/100 stars
      Buy from Supplier

    86
    Novogene strand specific transcriptome library preparation
    a Schematic illustration of the <t>RNA-seq</t> and metabolomics analyses. b Gene cluster trend in different groups ( n = 3 mice). c GO enrichment analysis of genes in cluster 1. d GO enrichment analysis of genes in cluster 3. e GO enrichment analysis of genes in cluster 4. GO enrichment analysis was performed using a one-sided hypergeo metric test. Terms with a p < 0.05 were considered significantly enriched. f Heatmap o f the relative abundance of proinflammatory cytokines and purine metabolic genes in the three groups ( n = 3 mice). g PCA score plot of different groups subjected to metabolic analysis. h Pathway enrichment analysis of the DEMs enriched in ALI mice treated with ND@Monos (vs. the ALI group). Significance of enrichment was determined by a hypergeometric test with an FDR-corrected p -value ( q -value) threshold of 0.05. i , j Western blot analysis and quantification of IL-1β, P-creb and P-P65 levels ( n = 5 mice). Data are presented as mean ± SD. NC group indicates normal mice, and PBS indicates mice treated with vehicle. Statistical analysis was performed by one-way ANOVA with Tukey’s multiple comparison test. Source data are provided as a Source Data file.
    Strand Specific Transcriptome Library Preparation, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transcriptomic+libraries/library+preparation+specific+strand+transcriptome/pmc12787643-361-0-7
    Average 86 stars, based on 1 article reviews
    strand specific transcriptome library preparation - by Bioz Stars, 2026-10
    86/100 stars
      Buy from Supplier

    Image Search Results


    Changes in intestinal short chain fatty acids and spleen transcriptome in mice treated with SYD. (A) The boxplot of acetic acid abundance among three groups; (B) The boxplot of isobutyric acid abundance among three groups; (C) Differences in PISA scores among the three groups; (D) Differences in body weight among three groups of mice; (E) and (F) The difference in thickness between the left and right ears of mice among the three groups; (G) The correlation between short chain fatty acids and phenotype indicators in mice, yellow represents positive correlation, blue represents negative correlation, and darker colors indicate higher correlation coefficients; (H) The volcano plot of transcriptome between Psoriasis and SYD Treatment groups; (I) The heatmap of inflammation related genes among significant differentially expressed genes; (J) The dot plot of GO enrichment analysis of upregulated genes; (K) The GSEA analysis of the G protein-coupled receptor signaling pathway; (L) The analysis of CIBERSORT, which displayed the relative abundance of different cell subpopulations in three groups; (M) The box plot shows significant differences in the abundance of plasma, Treg, and Tfh cell subpopulations among the three groups.

    Journal: Frontiers in Microbiology

    Article Title: Sanyin decoction alleviates psoriasis by reshaping gut microbiota and modulating the gut–spleen–skin axis

    doi: 10.3389/fmicb.2026.1799928

    Figure Lengend Snippet: Changes in intestinal short chain fatty acids and spleen transcriptome in mice treated with SYD. (A) The boxplot of acetic acid abundance among three groups; (B) The boxplot of isobutyric acid abundance among three groups; (C) Differences in PISA scores among the three groups; (D) Differences in body weight among three groups of mice; (E) and (F) The difference in thickness between the left and right ears of mice among the three groups; (G) The correlation between short chain fatty acids and phenotype indicators in mice, yellow represents positive correlation, blue represents negative correlation, and darker colors indicate higher correlation coefficients; (H) The volcano plot of transcriptome between Psoriasis and SYD Treatment groups; (I) The heatmap of inflammation related genes among significant differentially expressed genes; (J) The dot plot of GO enrichment analysis of upregulated genes; (K) The GSEA analysis of the G protein-coupled receptor signaling pathway; (L) The analysis of CIBERSORT, which displayed the relative abundance of different cell subpopulations in three groups; (M) The box plot shows significant differences in the abundance of plasma, Treg, and Tfh cell subpopulations among the three groups.

    Article Snippet: High-quality RNA was subsequently used for transcriptome library construction using the MGIEasy Fast RNA Reagent (MGI, 940-002921-00), mRNA was enriched using oligo (dT) magnetic beads, followed by fragmentation with fragmentation buffer at a controlled temperature.

    Techniques: Clinical Proteomics

    Changes in transcriptome of mouse skin after SYD treatment. (A) The volcano of differentially expressed genes; (B) The GO bioprocess (BP) analysis of significant upregulated genes; (C) The KEGG analysis of significant upregulated genes; (D) The GO molecular function (MF) analysis of significant upregulated genes; (E)-(H) The GSEA enrichment of significant regulated genes, NES < 0, represents downregulated signaling pathway, adjusted p value < 0.05, represents statistically significant; (I) The GSEA enrichment of upregulated signaling pathway; (J) The result of skin immune infiltration between Psoriasis group and Treatment group using CIBERSORT; (K) Boxplot of significant differences in immune cell subpopulations (Macrophage_M2, Neutrophils, Dendritic resting_cells).

    Journal: Frontiers in Microbiology

    Article Title: Sanyin decoction alleviates psoriasis by reshaping gut microbiota and modulating the gut–spleen–skin axis

    doi: 10.3389/fmicb.2026.1799928

    Figure Lengend Snippet: Changes in transcriptome of mouse skin after SYD treatment. (A) The volcano of differentially expressed genes; (B) The GO bioprocess (BP) analysis of significant upregulated genes; (C) The KEGG analysis of significant upregulated genes; (D) The GO molecular function (MF) analysis of significant upregulated genes; (E)-(H) The GSEA enrichment of significant regulated genes, NES < 0, represents downregulated signaling pathway, adjusted p value < 0.05, represents statistically significant; (I) The GSEA enrichment of upregulated signaling pathway; (J) The result of skin immune infiltration between Psoriasis group and Treatment group using CIBERSORT; (K) Boxplot of significant differences in immune cell subpopulations (Macrophage_M2, Neutrophils, Dendritic resting_cells).

    Article Snippet: High-quality RNA was subsequently used for transcriptome library construction using the MGIEasy Fast RNA Reagent (MGI, 940-002921-00), mRNA was enriched using oligo (dT) magnetic beads, followed by fragmentation with fragmentation buffer at a controlled temperature.

    Techniques:

    a Schematic illustration of the RNA-seq and metabolomics analyses. b Gene cluster trend in different groups ( n = 3 mice). c GO enrichment analysis of genes in cluster 1. d GO enrichment analysis of genes in cluster 3. e GO enrichment analysis of genes in cluster 4. GO enrichment analysis was performed using a one-sided hypergeo metric test. Terms with a p < 0.05 were considered significantly enriched. f Heatmap o f the relative abundance of proinflammatory cytokines and purine metabolic genes in the three groups ( n = 3 mice). g PCA score plot of different groups subjected to metabolic analysis. h Pathway enrichment analysis of the DEMs enriched in ALI mice treated with ND@Monos (vs. the ALI group). Significance of enrichment was determined by a hypergeometric test with an FDR-corrected p -value ( q -value) threshold of 0.05. i , j Western blot analysis and quantification of IL-1β, P-creb and P-P65 levels ( n = 5 mice). Data are presented as mean ± SD. NC group indicates normal mice, and PBS indicates mice treated with vehicle. Statistical analysis was performed by one-way ANOVA with Tukey’s multiple comparison test. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: A DNA-based nanodevice senses purinergic signaling and drives an immune switch for resolving inflammation

    doi: 10.1038/s41467-026-68879-2

    Figure Lengend Snippet: a Schematic illustration of the RNA-seq and metabolomics analyses. b Gene cluster trend in different groups ( n = 3 mice). c GO enrichment analysis of genes in cluster 1. d GO enrichment analysis of genes in cluster 3. e GO enrichment analysis of genes in cluster 4. GO enrichment analysis was performed using a one-sided hypergeo metric test. Terms with a p < 0.05 were considered significantly enriched. f Heatmap o f the relative abundance of proinflammatory cytokines and purine metabolic genes in the three groups ( n = 3 mice). g PCA score plot of different groups subjected to metabolic analysis. h Pathway enrichment analysis of the DEMs enriched in ALI mice treated with ND@Monos (vs. the ALI group). Significance of enrichment was determined by a hypergeometric test with an FDR-corrected p -value ( q -value) threshold of 0.05. i , j Western blot analysis and quantification of IL-1β, P-creb and P-P65 levels ( n = 5 mice). Data are presented as mean ± SD. NC group indicates normal mice, and PBS indicates mice treated with vehicle. Statistical analysis was performed by one-way ANOVA with Tukey’s multiple comparison test. Source data are provided as a Source Data file.

    Article Snippet: The RNA sequencing transcriptome library was generated with a TruSeq TM RNA sample preparation kit from Illumina (San Diego, CA). cDNA was synthesized via a SuperScript double-stranded cDNA synthesis kit (Invitrogen) with random hexamer primers (Illumina).

    Techniques: RNA Sequencing, Western Blot, Comparison