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sham-operated adx mice  (Jackson Laboratory)

 
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    Jackson Laboratory sham-operated adx mice
    (A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from <t>CD45.2</t> + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).
    Sham Operated Adx Mice, supplied by Jackson Laboratory, 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/result/sham-operated adx mice/product/Jackson Laboratory
    Average 90 stars, based on 1 article reviews
    sham-operated adx mice - by Bioz Stars, 2026-02
    90/100 stars

    Images

    1) Product Images from "Genomic Analysis of Progenitors in Viral Infection Implicates Glucocorticoids as Suppressors of Plasmacytoid Dendritic Cell Generation"

    Article Title: Genomic Analysis of Progenitors in Viral Infection Implicates Glucocorticoids as Suppressors of Plasmacytoid Dendritic Cell Generation

    Journal: bioRxiv

    doi: 10.1101/2024.10.28.620771

    (A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from CD45.2 + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).
    Figure Legend Snippet: (A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from CD45.2 + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).

    Techniques Used: Isolation, Infection, Flow Cytometry, Purification, RNA Sequencing Assay



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    (A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from <t>CD45.2</t> + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).
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    (A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from <t>CD45.2</t> + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).
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    (A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from <t>CD45.2</t> + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).
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    Image Search Results


    (A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from CD45.2 + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).

    Journal: bioRxiv

    Article Title: Genomic Analysis of Progenitors in Viral Infection Implicates Glucocorticoids as Suppressors of Plasmacytoid Dendritic Cell Generation

    doi: 10.1101/2024.10.28.620771

    Figure Lengend Snippet: (A) Conceptual and non-proportional diagram of the continuous model of DC hematopoiesis. Lin − c-kit int/lo Flt3 + progenitors are outlined in red. Classically defined progenitor populations (CD115+ CDP (CDP M+ ), CD115-CDP (CDP M- ), CLP, black boxes) partially overlap in potential. (B) Lin − c-kit int/lo Flt3 + progenitors were isolated from CD45.2 + mice infected with LCMV Cl13 at day 8 p.i., or mice that were left uninfected (Un) and transferred into infection matched or Un controls, respectively. Eight days after transfer, spleens were harvested, and DC development assessed by flow cytometry. (C-H) C57BL6/J mice were infected with LCMV ARM or Cl13 or left uninfected (Un), sacrificed at day 8 p.i., and Lin − c-kit int/lo Flt3 + progenitors were FACS-purified from BM for RNA-seq (D-E) and ATAC-seq (F-H) analyses. Data are representative of three independent repeats, each with 3-5 mice pooled per group. (D) Hierarchical clustering of RNA-seq profiles on the whole transcriptome by using Pearson correlation. (E) Venn diagram showing overlap between differentially expressed genes (DEGs) from Cl13 vs. Un and ARM vs. Un comparisons. (F) Hierarchical clustering of ATAC-seq profiles by using Pearson correlation. (G) Venn diagram showing overlap between differentially accessible (DA) chromatin regions from Cl13 vs. Un and ARM vs. Un comparisons. (H) Number of differential peaks that opened (left, red; right, green) or closed (blue) during infection. Graphs depict means ± SEM and symbols represent individual mice. (B) Data are pooled from two independent experiments with 2– 4 mice/group. (D-H) Data are representative of three independent repeats, each with 3-5 mice pooled per group. * p < 0.05, ****p < 0.0001. Statistical significance was determined by unpaired student’s t-test (B).

    Article Snippet: C57BL6/J mice, CD45.1 + mice, sham-operated and ADX mice (7-8 weeks old) were purchased from The Jackson Laboratory.

    Techniques: Isolation, Infection, Flow Cytometry, Purification, RNA Sequencing Assay