mouse serum innovative research inc Search Results


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(A) Bacterial recovery of the indicated strains from the kidneys and peritoneal cavity of <t>Swiss</t> <t>Webster</t> <t>mice</t> 24 h after intraperitoneal injection ( n = 24). * p < 0.05 and ***, p < 0.001, calculated by the Kruskal-Wallis test with Dunn’s multiple comparisons test. (B) Bacterial recovery of the indicated strains from the kidneys of C57BL/6 mice 24 h after bloodstream infection ( n = 16). * p < 0.05 and ** p < 0.01 by Kruskal-Wallis test with Dunn’s multiple comparisons test. (C) Bacterial recovery of the indicated strains from the peritoneal cavity of C57BL/6 and Cybb − mice 24 h after intraperitoneal injection with 1 × 10 8 CFUs ( n = 20) or 1 × 10 7 CFUs ( n = 10). ** p < 0.01, *** p < 0.001 by unpaired t test (1 × 10 8 CFUs) or Mann-Whitney test (1 × 10 7 CFUs). (D) Outgrowth of the indicated strains after infection with isolated macrophages from Swiss Webster mice. (E) Outgrowth of the indicated strains after infection with isolated macrophages from Swiss Webster mice that were treated with vehicle control (water) or the NADPH oxidase inhibitor gp91ds-tat (50 μM). (F) Outgrowth of the indicated strains after infection with isolated macrophages from C57BL/6 and Cybb − mice. ** p < 0.01, *** p < 0.001, **** p < 0.0001 by two-way ANOVA with Tukey’s post hoc test (D–F). Data are represented as individual values with the median indicated as a solid line.
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Innovative Research Inc mouse serum complement
Figure 1. Preparation of the positive control. The positive control was used as quality control in the enzyme-linked immunosorbent assay (ELISA). Mouse serum con- taining mouse immunoglobulin (Ig) and inactivated <t>complement</t> was incubated with heat-aggregated human IgG (“Complement Activator”) to stimulate complement activation by the classical complement pathway. Monomeric mouse IgG was able to bind to aggregated human IgG, leading to formation of complement bound hIgG-mIgG complexes. HRP (horse radish peroxidase) signal.
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Innovative Research Inc alysis buffer cd 1 mouse serum innovativeresearch
Figure 1. Preparation of the positive control. The positive control was used as quality control in the enzyme-linked immunosorbent assay (ELISA). Mouse serum con- taining mouse immunoglobulin (Ig) and inactivated <t>complement</t> was incubated with heat-aggregated human IgG (“Complement Activator”) to stimulate complement activation by the classical complement pathway. Monomeric mouse IgG was able to bind to aggregated human IgG, leading to formation of complement bound hIgG-mIgG complexes. HRP (horse radish peroxidase) signal.
Alysis Buffer Cd 1 Mouse Serum Innovativeresearch, supplied by Innovative Research Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Figure 1. Preparation of the positive control. The positive control was used as quality control in the enzyme-linked immunosorbent assay (ELISA). Mouse serum con- taining mouse immunoglobulin (Ig) and inactivated <t>complement</t> was incubated with heat-aggregated human IgG (“Complement Activator”) to stimulate complement activation by the classical complement pathway. Monomeric mouse IgG was able to bind to aggregated human IgG, leading to formation of complement bound hIgG-mIgG complexes. HRP (horse radish peroxidase) signal.
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Figure 1. Preparation of the positive control. The positive control was used as quality control in the enzyme-linked immunosorbent assay (ELISA). Mouse serum con- taining mouse immunoglobulin (Ig) and inactivated <t>complement</t> was incubated with heat-aggregated human IgG (“Complement Activator”) to stimulate complement activation by the classical complement pathway. Monomeric mouse IgG was able to bind to aggregated human IgG, leading to formation of complement bound hIgG-mIgG complexes. HRP (horse radish peroxidase) signal.
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Innovative Research Inc mouse serum albumin
Figure 1. Preparation of the positive control. The positive control was used as quality control in the enzyme-linked immunosorbent assay (ELISA). Mouse serum con- taining mouse immunoglobulin (Ig) and inactivated <t>complement</t> was incubated with heat-aggregated human IgG (“Complement Activator”) to stimulate complement activation by the classical complement pathway. Monomeric mouse IgG was able to bind to aggregated human IgG, leading to formation of complement bound hIgG-mIgG complexes. HRP (horse radish peroxidase) signal.
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Image Search Results


(A) Bacterial recovery of the indicated strains from the kidneys and peritoneal cavity of Swiss Webster mice 24 h after intraperitoneal injection ( n = 24). * p < 0.05 and ***, p < 0.001, calculated by the Kruskal-Wallis test with Dunn’s multiple comparisons test. (B) Bacterial recovery of the indicated strains from the kidneys of C57BL/6 mice 24 h after bloodstream infection ( n = 16). * p < 0.05 and ** p < 0.01 by Kruskal-Wallis test with Dunn’s multiple comparisons test. (C) Bacterial recovery of the indicated strains from the peritoneal cavity of C57BL/6 and Cybb − mice 24 h after intraperitoneal injection with 1 × 10 8 CFUs ( n = 20) or 1 × 10 7 CFUs ( n = 10). ** p < 0.01, *** p < 0.001 by unpaired t test (1 × 10 8 CFUs) or Mann-Whitney test (1 × 10 7 CFUs). (D) Outgrowth of the indicated strains after infection with isolated macrophages from Swiss Webster mice. (E) Outgrowth of the indicated strains after infection with isolated macrophages from Swiss Webster mice that were treated with vehicle control (water) or the NADPH oxidase inhibitor gp91ds-tat (50 μM). (F) Outgrowth of the indicated strains after infection with isolated macrophages from C57BL/6 and Cybb − mice. ** p < 0.01, *** p < 0.001, **** p < 0.0001 by two-way ANOVA with Tukey’s post hoc test (D–F). Data are represented as individual values with the median indicated as a solid line.

Journal: Cell reports

Article Title: Staphylococcus aureus exploits lipoic acid salvage to combat host oxidative stress

doi: 10.1016/j.celrep.2025.116095

Figure Lengend Snippet: (A) Bacterial recovery of the indicated strains from the kidneys and peritoneal cavity of Swiss Webster mice 24 h after intraperitoneal injection ( n = 24). * p < 0.05 and ***, p < 0.001, calculated by the Kruskal-Wallis test with Dunn’s multiple comparisons test. (B) Bacterial recovery of the indicated strains from the kidneys of C57BL/6 mice 24 h after bloodstream infection ( n = 16). * p < 0.05 and ** p < 0.01 by Kruskal-Wallis test with Dunn’s multiple comparisons test. (C) Bacterial recovery of the indicated strains from the peritoneal cavity of C57BL/6 and Cybb − mice 24 h after intraperitoneal injection with 1 × 10 8 CFUs ( n = 20) or 1 × 10 7 CFUs ( n = 10). ** p < 0.01, *** p < 0.001 by unpaired t test (1 × 10 8 CFUs) or Mann-Whitney test (1 × 10 7 CFUs). (D) Outgrowth of the indicated strains after infection with isolated macrophages from Swiss Webster mice. (E) Outgrowth of the indicated strains after infection with isolated macrophages from Swiss Webster mice that were treated with vehicle control (water) or the NADPH oxidase inhibitor gp91ds-tat (50 μM). (F) Outgrowth of the indicated strains after infection with isolated macrophages from C57BL/6 and Cybb − mice. ** p < 0.01, *** p < 0.001, **** p < 0.0001 by two-way ANOVA with Tukey’s post hoc test (D–F). Data are represented as individual values with the median indicated as a solid line.

Article Snippet: Mouse Swiss Webster serum , Innovative Research Inc , Cat # 50-203-5738.

Techniques: Injection, Infection, MANN-WHITNEY, Isolation, Control

Figure 1. Preparation of the positive control. The positive control was used as quality control in the enzyme-linked immunosorbent assay (ELISA). Mouse serum con- taining mouse immunoglobulin (Ig) and inactivated complement was incubated with heat-aggregated human IgG (“Complement Activator”) to stimulate complement activation by the classical complement pathway. Monomeric mouse IgG was able to bind to aggregated human IgG, leading to formation of complement bound hIgG-mIgG complexes. HRP (horse radish peroxidase) signal.

Journal: Journal of Immunotoxicology

Article Title: An ELISA for detection of complement-bound circulating immune complexes in mice

doi: 10.1080/1547691x.2019.1599471

Figure Lengend Snippet: Figure 1. Preparation of the positive control. The positive control was used as quality control in the enzyme-linked immunosorbent assay (ELISA). Mouse serum con- taining mouse immunoglobulin (Ig) and inactivated complement was incubated with heat-aggregated human IgG (“Complement Activator”) to stimulate complement activation by the classical complement pathway. Monomeric mouse IgG was able to bind to aggregated human IgG, leading to formation of complement bound hIgG-mIgG complexes. HRP (horse radish peroxidase) signal.

Article Snippet: In brief, mouse serum complement (Innovative Research, Novi, MI, cat. no IMS-C57BL6-COMPL) was incubated at 37 C for 90min with 1:100 HAGG (Complement Activator, Quidel, San Diego, CA, cat. #A114), followed by inactivation by addition of ice-cold 500mM ethylenediamine-tetraacetic acid (EDTA; to final concentration of 20mM) and storage (undiluted) at 80 C until analysis.

Techniques: Positive Control, Control, Enzyme-linked Immunosorbent Assay, Incubation, Activation Assay