dba 2jrj mice (Janvier Labs)
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Dba 2jrj Mice, supplied by Janvier Labs, 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/dba/1+dba+mice/pm42270907-35-2-7
Average 86 stars, based on 1 article reviews
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Sequencing:Article Title: Microbiota-specific serum IgG links gut and joints through immune–endothelial crosstalk in arthritis Article Snippet: Five to six-week-old Article Title: Histamine H3 Receptor as a target for alcohol use disorder: challenging the predictability of animal models for clinical translation in drug development. Article Snippet: 50 μL of Working Detection Solution (19 parts of Cell Assay Buffer, five parts of Substrate Reagent 1 and one-part Substrate Reagent 2, DiscoverX PathHunter detection kit 93-001) were added followed by a 1-hour incubation at room temperature in the dark for the reaction to occur. Endpoint Dilution Assay:Article Title: Microbiota-specific serum IgG links gut and joints through immune–endothelial crosstalk in arthritis Article Snippet: Five to six-week-old Article Title: Histamine H3 Receptor as a target for alcohol use disorder: challenging the predictability of animal models for clinical translation in drug development. Article Snippet: 50 μL of Working Detection Solution (19 parts of Cell Assay Buffer, five parts of Substrate Reagent 1 and one-part Substrate Reagent 2, DiscoverX PathHunter detection kit 93-001) were added followed by a 1-hour incubation at room temperature in the dark for the reaction to occur. Serial Dilution:Article Title: Microbiota-specific serum IgG links gut and joints through immune–endothelial crosstalk in arthritis Article Snippet: Five to six-week-old Article Title: Histamine H3 Receptor as a target for alcohol use disorder: challenging the predictability of animal models for clinical translation in drug development. Article Snippet: 50 μL of Working Detection Solution (19 parts of Cell Assay Buffer, five parts of Substrate Reagent 1 and one-part Substrate Reagent 2, DiscoverX PathHunter detection kit 93-001) were added followed by a 1-hour incubation at room temperature in the dark for the reaction to occur. Enzyme-linked Immunosorbent Assay:Article Title: Microbiota-specific serum IgG links gut and joints through immune–endothelial crosstalk in arthritis Article Snippet: Five to six-week-old Article Title: Histamine H3 Receptor as a target for alcohol use disorder: challenging the predictability of animal models for clinical translation in drug development. Article Snippet: 50 μL of Working Detection Solution (19 parts of Cell Assay Buffer, five parts of Substrate Reagent 1 and one-part Substrate Reagent 2, DiscoverX PathHunter detection kit 93-001) were added followed by a 1-hour incubation at room temperature in the dark for the reaction to occur. Comparison:Article Title: Microbiota-specific serum IgG links gut and joints through immune–endothelial crosstalk in arthritis Article Snippet: Five to six-week-old Article Title: Histamine H3 Receptor as a target for alcohol use disorder: challenging the predictability of animal models for clinical translation in drug development. Article Snippet: 50 μL of Working Detection Solution (19 parts of Cell Assay Buffer, five parts of Substrate Reagent 1 and one-part Substrate Reagent 2, DiscoverX PathHunter detection kit 93-001) were added followed by a 1-hour incubation at room temperature in the dark for the reaction to occur. MANN-WHITNEY:Article Title: Microbiota-specific serum IgG links gut and joints through immune–endothelial crosstalk in arthritis Article Snippet: Five to six-week-old Article Title: Histamine H3 Receptor as a target for alcohol use disorder: challenging the predictability of animal models for clinical translation in drug development. Article Snippet: 50 μL of Working Detection Solution (19 parts of Cell Assay Buffer, five parts of Substrate Reagent 1 and one-part Substrate Reagent 2, DiscoverX PathHunter detection kit 93-001) were added followed by a 1-hour incubation at room temperature in the dark for the reaction to occur. Isolation:Article Title: Microbiota-specific serum IgG links gut and joints through immune–endothelial crosstalk in arthritis Article Snippet: Five to six-week-old Article Title: Histamine H3 Receptor as a target for alcohol use disorder: challenging the predictability of animal models for clinical translation in drug development. Article Snippet: 50 μL of Working Detection Solution (19 parts of Cell Assay Buffer, five parts of Substrate Reagent 1 and one-part Substrate Reagent 2, DiscoverX PathHunter detection kit 93-001) were added followed by a 1-hour incubation at room temperature in the dark for the reaction to occur. Virus:Article Title: Microbiota-specific serum IgG links gut and joints through immune–endothelial crosstalk in arthritis Article Snippet: Five to six-week-old Article Title: Histamine H3 Receptor as a target for alcohol use disorder: challenging the predictability of animal models for clinical translation in drug development. Article Snippet: 50 μL of Working Detection Solution (19 parts of Cell Assay Buffer, five parts of Substrate Reagent 1 and one-part Substrate Reagent 2, DiscoverX PathHunter detection kit 93-001) were added followed by a 1-hour incubation at room temperature in the dark for the reaction to occur. Injection:Article Title: Microbiota-specific serum IgG links gut and joints through immune–endothelial crosstalk in arthritis Article Snippet: Five to six-week-old Article Title: Histamine H3 Receptor as a target for alcohol use disorder: challenging the predictability of animal models for clinical translation in drug development. Article Snippet: 50 μL of Working Detection Solution (19 parts of Cell Assay Buffer, five parts of Substrate Reagent 1 and one-part Substrate Reagent 2, DiscoverX PathHunter detection kit 93-001) were added followed by a 1-hour incubation at room temperature in the dark for the reaction to occur. |
![Phenotypic Characterization of Collagen Induced Arthritis <t>in</t> <t>DBA/1J</t> Mice. DBA/1J mice were immunized with bovine type II collagen (N = 11–55; arthritic: n = 6–18; non-arthritic: n = 5–37) or PBS (N = 4–14). A) Representative photographs and E) 3D-rendered micro-CT radiographs of arthritic (red arrow = bone erosion), non-arthritic, and PBS-injected mouse hind limbs. Changes in B) clinical arthritis score, C) anti-bovine type II collagen (CII) IgG and D) anti-mouse CII IgG over time. Dashed line represents the antibody positivity cut-off, indicating the limit of detection. F) Hind limb bone mineral density and G) bone mineral density of bCII-immunized fore and hind limbs over time. H) Pain-like behaviour at day 47 post primary immunization. Graphs show the median [IQR], with each symbol in F-H) representing an individual mouse. For B-D), statistical analysis was performed using a mixed effects model with the Geisser-Greenhouse correction and Tukey's multiple comparisons test, with resulting p-values shown in the graphs. Kruskal-Wallis with Dunn's multiple comparisons test was used for F) and H), and the resulting p-values were p = 0.0008 and p = 0.0003 respectively, with p-values for pairwise comparisons indicated on the graphs. For G), a Spearman correlation coefficient (r) was calculated and p < 0.05 was considered significant.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_0342/pmc12810342/pmc12810342__gr1.jpg)
