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mouse ige elisa quantification kit  (Beijing Solarbio Science)


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    Beijing Solarbio Science mouse ige elisa quantification kit
    Mouse Ige Elisa Quantification Kit, supplied by Beijing Solarbio Science, 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+ige+quantification+kit/mouse+ige+elisa+kit+sekm+0095/pm33692106-329-7-13
    Average 90 stars, based on 1 article reviews
    mouse ige elisa quantification kit - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Isolation of the novel phage SAP71 and its potential use against Staphylococcus aureus in an atopic dermatitis mouse model.
    Article Snippet: Atopic dermatitis (AD) is accompanied by changes in skin microbiota, in which abnormal colonization of Staphylococcus aureus is particularly common.. The antibiotic treatment is prone to destroy the commensal bacterial community, further exacerbating the microbiome dysbiosis.. Elimination of S. aureus through phage-targeted therapies presents a promising method in the treatment strategy of AD.

    Article Title: Macrophage-derived amphiregulin promoted the osteogenic differentiation of chondrocytes through EGFR/Yap axis and TGF-β activation.
    Article Snippet: Endochondral ossification represents a crucial biological process in skeletal development and bone defect repair.. Macrophages, recognized as key players in the immune system, are now acknowledged for their substantial role in promoting endochondral ossification within cartilage.. Concurrently, the epidermal growth factor receptor (EGFR) ligand amphiregulin (Areg) has been documented for its contributory role in restoring bone tissue homeostasis post-injury.

    Article Title: In vivo immunological activity of chitosan-derived nanoparticles.
    Article Snippet: Chitosan has been studied as an immunomodulator, but few studies have used chitosan derivatives as adjuvants alone.. After a preliminary study, we found that nanoparticles prepared from chitosan derivatives had better cellular immune activity when used as an adjuvant.. Therefore, animal experiments were conducted to further investigate the performance and mechanism of these nanoparticles as immune adjuvants.

    Article Title: Operation-friendly and accurate naked-eye observation assay for fast zoonotic echinococcosis and pulmonary tuberculosis monitoring in clinics.
    Article Snippet: • Construct an operation-friendly ELISA integrating magnetic separation and plasma luminescence.. • Simplify the time-consuming and equipment-intensive processes of con-

    Article Title: Usp11 maintained the survival of marginal zone B cells under ionizing radiation by deubiquitinating DLL1 and JAG2
    Article Snippet: .. Serum IgM and IgG were validated by mouse IgM ELISA assay (Solarbio, China) and IgG ELISA assay (Neobioscience, China) according to manufacturer’s protocols [ ]. .. Antibodies used for flow cytometry staining include anti-CD45-Alexa Fluor 700 (1:400 BioLegend, USA), anti-CD19-APC (1:400 BioLegend, USA), anti-CD23-PE-Cy7 (1:400 eBioscience, USA), anti-CD21-FITC (1:400 BioLegend, USA), and anti-CD45R(B220) (1:400 BioLegend, USA), anti-IgM-FITC (1: 400 eBioscience, USA) (Supplementary Table ).

    other:

    Article Title: Helicobacter mastomyrinus infection induces autoimmune hepatitis in mice
    Article Snippet: In order to determine the IgG content, the mouse sera were initially diluted 100-fold and subsequently employed in the mouse IgG (total) ELISA kit (Solarbio, Beijing, China).

    Article Title: Contriving a novel of CHB therapeutic vaccine based on IgV_CTLA-4 and L protein via immunoinformatics approach.
    Article Snippet: The Mouse IgG (Total) ELISA kit (SEKM-0098, Solarbio, Beijing, China) was used to this experiment, and the experiment operation strictly followed the kit instruction.

    Article Title: Design a novel of Brucellosis preventive vaccine based on IgV_CTLA-4 and multiple epitopes via immunoinformatics approach.
    Article Snippet: Brucellosis is a zoonotic disease caused by Brucella, which is difficult to eliminate by conventional drugs.. Therefore, a novel multi-epitope vaccine (MEV) was designed to prevent human Brucella infection.. Based on the method of “reverse vaccinology”, cytotoxic T lymphocyte epitopes (CTLEs), helper T lymphocyte epitopes (HTLEs), linear B-cell epitopes (LBEs) and conformational B-cell epitopes (CBEs) of four Brucella proteins (VirB9, VirB10, Omp 19 and Omp 25) were obtained.

    Clinical Proteomics:

    Article Title: Operation-friendly and accurate naked-eye observation assay for fast zoonotic echinococcosis and pulmonary tuberculosis monitoring in clinics.
    Article Snippet: • Construct an operation-friendly ELISA integrating magnetic separation and plasma luminescence.. • Simplify the time-consuming and equipment-intensive processes of con-



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    Figure 4 Sensitization of GF and Lmix-colonized mice with the major birch pollen allergen Bet v 1. (a) The experimental design was as follows: 8-week- old GF mice (n512) were divided into two groups. The first group (Lmix) received an equal-part mixture (23108 CFU/ml) of L. rhamnosus LOCK0900, L. rhamnosus LOCK0908 and L. casei LOCK0919 by intragastric tubing. The second group was kept GF. Mice were sensitized three times intra- peritoneally with recombinant Bet v 1 (1 mg in alum) on days 77, 87 and 97. One week after the last immunization (day 104), tissue samples were collected for further analyses. Bacterial colonization of the Lmix-colonized mice was evaluated on the first 2 days and then at weekly intervals throughout the experiment. At the species level, bacteria were distinguished based on colony morphology by the cultivation of appropriate serial dilutions of the fecal samples. (b) L. casei LOCK0919 (full circles, solid line), L. rhamnosus LOCK0900 and LOCK0908 (open squares, dotted line). L. rhamnosus strain- specific discrimination was performed by qPCR using DNA isolated from the fecal samples at the indicated time points (c) L. rhamnosus LOCK0900 (gray bars) and L. rhamnosus LOCK0908 (black bars). The data are shown as a percentage of each strain out of all detected L. rhamnosus bacteria on the indicated day after colonization. Bet v 1-specific antibodies were measured in the sera of GF (white bars) and Lmix-colonized mice (black <t>bars).</t> <t>IgE</t> was measured by Bet v 1-mediated b-hexosaminidase release from rat basophil leukemia cells (d). Levels of IgG1 (e) and IgG2a (f) were evaluated by <t>ELISA</t> and expressed as OD units. The data are shown as the mean6s.e.m. One representative out of two experiments is shown; n56/group. *P,0.05 and **P,0.01. GF, germ-free; Ig, immunoglobulin; i.p., intraperitoneally; Lmix, Lactobacillus mixture; OD, optical density.
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    Figure 4 Sensitization of GF and Lmix-colonized mice with the major birch pollen allergen Bet v 1. (a) The experimental design was as follows: 8-week- old GF mice (n512) were divided into two groups. The first group (Lmix) received an equal-part mixture (23108 CFU/ml) of L. rhamnosus LOCK0900, L. rhamnosus LOCK0908 and L. casei LOCK0919 by intragastric tubing. The second group was kept GF. Mice were sensitized three times intra- peritoneally with recombinant Bet v 1 (1 mg in alum) on days 77, 87 and 97. One week after the last immunization (day 104), tissue samples were collected for further analyses. Bacterial colonization of the Lmix-colonized mice was evaluated on the first 2 days and then at weekly intervals throughout the experiment. At the species level, bacteria were distinguished based on colony morphology by the cultivation of appropriate serial dilutions of the fecal samples. (b) L. casei LOCK0919 (full circles, solid line), L. rhamnosus LOCK0900 and LOCK0908 (open squares, dotted line). L. rhamnosus strain- specific discrimination was performed by qPCR using DNA isolated from the fecal samples at the indicated time points (c) L. rhamnosus LOCK0900 (gray bars) and L. rhamnosus LOCK0908 (black bars). The data are shown as a percentage of each strain out of all detected L. rhamnosus bacteria on the indicated day after colonization. Bet v 1-specific antibodies were measured in the sera of GF (white bars) and Lmix-colonized mice (black <t>bars).</t> <t>IgE</t> was measured by Bet v 1-mediated b-hexosaminidase release from rat basophil leukemia cells (d). Levels of IgG1 (e) and IgG2a (f) were evaluated by <t>ELISA</t> and expressed as OD units. The data are shown as the mean6s.e.m. One representative out of two experiments is shown; n56/group. *P,0.05 and **P,0.01. GF, germ-free; Ig, immunoglobulin; i.p., intraperitoneally; Lmix, Lactobacillus mixture; OD, optical density.
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    Image Search Results


    Levels of OVA ‐specific IgE (A), IgG2a (B), IgG1 (C) and IgA (D) antibodies in serum, as measured by ELISA . Pooled values of two repeat experiments, each with four to six mice per group, are expressed as means ± SEM ; * P < 0.05, *** P < 0.001, **** P < 0.0001.

    Journal: Microbial Biotechnology

    Article Title: Polysaccharides L900/2 and L900/3 isolated from Lactobacillus rhamnosus LOCK 0900 modulate allergic sensitization to ovalbumin in a mouse model

    doi: 10.1111/1751-7915.12606

    Figure Lengend Snippet: Levels of OVA ‐specific IgE (A), IgG2a (B), IgG1 (C) and IgA (D) antibodies in serum, as measured by ELISA . Pooled values of two repeat experiments, each with four to six mice per group, are expressed as means ± SEM ; * P < 0.05, *** P < 0.001, **** P < 0.0001.

    Article Snippet: The serum levels of total IgA and IgE were measured using a mouse IgA and IgE ELISA quantification kit (Bethyl, Montgomery, TX, USA) according to the manufacturer's instructions.

    Techniques: Enzyme-linked Immunosorbent Assay

    Levels of total IgE (A) and IgA (B) in serum, as measured by ELISA . Pooled values of two repeat experiments, each with four to six mice per group.

    Journal: Microbial Biotechnology

    Article Title: Polysaccharides L900/2 and L900/3 isolated from Lactobacillus rhamnosus LOCK 0900 modulate allergic sensitization to ovalbumin in a mouse model

    doi: 10.1111/1751-7915.12606

    Figure Lengend Snippet: Levels of total IgE (A) and IgA (B) in serum, as measured by ELISA . Pooled values of two repeat experiments, each with four to six mice per group.

    Article Snippet: The serum levels of total IgA and IgE were measured using a mouse IgA and IgE ELISA quantification kit (Bethyl, Montgomery, TX, USA) according to the manufacturer's instructions.

    Techniques: Enzyme-linked Immunosorbent Assay

    Figure 4 Sensitization of GF and Lmix-colonized mice with the major birch pollen allergen Bet v 1. (a) The experimental design was as follows: 8-week- old GF mice (n512) were divided into two groups. The first group (Lmix) received an equal-part mixture (23108 CFU/ml) of L. rhamnosus LOCK0900, L. rhamnosus LOCK0908 and L. casei LOCK0919 by intragastric tubing. The second group was kept GF. Mice were sensitized three times intra- peritoneally with recombinant Bet v 1 (1 mg in alum) on days 77, 87 and 97. One week after the last immunization (day 104), tissue samples were collected for further analyses. Bacterial colonization of the Lmix-colonized mice was evaluated on the first 2 days and then at weekly intervals throughout the experiment. At the species level, bacteria were distinguished based on colony morphology by the cultivation of appropriate serial dilutions of the fecal samples. (b) L. casei LOCK0919 (full circles, solid line), L. rhamnosus LOCK0900 and LOCK0908 (open squares, dotted line). L. rhamnosus strain- specific discrimination was performed by qPCR using DNA isolated from the fecal samples at the indicated time points (c) L. rhamnosus LOCK0900 (gray bars) and L. rhamnosus LOCK0908 (black bars). The data are shown as a percentage of each strain out of all detected L. rhamnosus bacteria on the indicated day after colonization. Bet v 1-specific antibodies were measured in the sera of GF (white bars) and Lmix-colonized mice (black bars). IgE was measured by Bet v 1-mediated b-hexosaminidase release from rat basophil leukemia cells (d). Levels of IgG1 (e) and IgG2a (f) were evaluated by ELISA and expressed as OD units. The data are shown as the mean6s.e.m. One representative out of two experiments is shown; n56/group. *P,0.05 and **P,0.01. GF, germ-free; Ig, immunoglobulin; i.p., intraperitoneally; Lmix, Lactobacillus mixture; OD, optical density.

    Journal: Cellular & molecular immunology

    Article Title: Colonization of germ-free mice with a mixture of three lactobacillus strains enhances the integrity of gut mucosa and ameliorates allergic sensitization.

    doi: 10.1038/cmi.2015.09

    Figure Lengend Snippet: Figure 4 Sensitization of GF and Lmix-colonized mice with the major birch pollen allergen Bet v 1. (a) The experimental design was as follows: 8-week- old GF mice (n512) were divided into two groups. The first group (Lmix) received an equal-part mixture (23108 CFU/ml) of L. rhamnosus LOCK0900, L. rhamnosus LOCK0908 and L. casei LOCK0919 by intragastric tubing. The second group was kept GF. Mice were sensitized three times intra- peritoneally with recombinant Bet v 1 (1 mg in alum) on days 77, 87 and 97. One week after the last immunization (day 104), tissue samples were collected for further analyses. Bacterial colonization of the Lmix-colonized mice was evaluated on the first 2 days and then at weekly intervals throughout the experiment. At the species level, bacteria were distinguished based on colony morphology by the cultivation of appropriate serial dilutions of the fecal samples. (b) L. casei LOCK0919 (full circles, solid line), L. rhamnosus LOCK0900 and LOCK0908 (open squares, dotted line). L. rhamnosus strain- specific discrimination was performed by qPCR using DNA isolated from the fecal samples at the indicated time points (c) L. rhamnosus LOCK0900 (gray bars) and L. rhamnosus LOCK0908 (black bars). The data are shown as a percentage of each strain out of all detected L. rhamnosus bacteria on the indicated day after colonization. Bet v 1-specific antibodies were measured in the sera of GF (white bars) and Lmix-colonized mice (black bars). IgE was measured by Bet v 1-mediated b-hexosaminidase release from rat basophil leukemia cells (d). Levels of IgG1 (e) and IgG2a (f) were evaluated by ELISA and expressed as OD units. The data are shown as the mean6s.e.m. One representative out of two experiments is shown; n56/group. *P,0.05 and **P,0.01. GF, germ-free; Ig, immunoglobulin; i.p., intraperitoneally; Lmix, Lactobacillus mixture; OD, optical density.

    Article Snippet: Total IgA and IgE responses Total IgA and IgE were measured in the sera and gut lavages (IgA only) with a mouse IgA and IgE ELISA quantification kit (Bethyl, Montgomery, TX, USA) according to manufacturer’s instructions.

    Techniques: Recombinant, Bacteria, Isolation, Enzyme-linked Immunosorbent Assay

    Figure 5 Local and systemic humoral responses in sensitized GF and Lmix-colonized mice. Levels of total IgE (a) and total IgA (b) in the sera and total IgA (c) in the gut lavage were measured by ELISA. Germ-free mice (GF, white bars) and Lmix-colonized mice (Lmix, black bars). The data are shown as the mean6s.e.m. One representative out of two experiments is shown; n56/group. *P,0.05 and **P,0.01. IgA-positive plasmocytes in the lamina propria of the terminal ileum were visualized with an FITC-labeled anti-IgA antibody (d). GF, germ-free; Ig, immunoglobulin; Lmix, Lactobacillus mixture.

    Journal: Cellular & molecular immunology

    Article Title: Colonization of germ-free mice with a mixture of three lactobacillus strains enhances the integrity of gut mucosa and ameliorates allergic sensitization.

    doi: 10.1038/cmi.2015.09

    Figure Lengend Snippet: Figure 5 Local and systemic humoral responses in sensitized GF and Lmix-colonized mice. Levels of total IgE (a) and total IgA (b) in the sera and total IgA (c) in the gut lavage were measured by ELISA. Germ-free mice (GF, white bars) and Lmix-colonized mice (Lmix, black bars). The data are shown as the mean6s.e.m. One representative out of two experiments is shown; n56/group. *P,0.05 and **P,0.01. IgA-positive plasmocytes in the lamina propria of the terminal ileum were visualized with an FITC-labeled anti-IgA antibody (d). GF, germ-free; Ig, immunoglobulin; Lmix, Lactobacillus mixture.

    Article Snippet: Total IgA and IgE responses Total IgA and IgE were measured in the sera and gut lavages (IgA only) with a mouse IgA and IgE ELISA quantification kit (Bethyl, Montgomery, TX, USA) according to manufacturer’s instructions.

    Techniques: Enzyme-linked Immunosorbent Assay, Labeling