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mouse ige quantification kit  (Fortis Life Sciences)


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    Structured Review

    Fortis Life Sciences mouse ige quantification kit
    Mouse Ige Quantification Kit, supplied by Fortis Life Sciences, used in various techniques. Bioz Stars score: 94/100, based on 352 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+ige+quantification+kit/Mouse+IgE+Antibody/pm28024292-127-5-9
    Average 94 stars, based on 352 article reviews
    mouse ige quantification kit - by Bioz Stars, 2026-10
    94/100 stars

    Images

    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Chaga Mushroom ( Inonotus obliquus ) Attenuates DNCB-Induced Atopic Dermatitis by Modulating Oxidative Stress and Cytokine Expression
    Article Snippet: .. Mouse IgE and IgG2a enzyme-linked immunosorbent assay (ELISA) kits were purchased from Bethyl Laboratories (USA). .. Polymerase chain reaction (PCR) primers were obtained from Genotech (Republic of Korea).

    Article Title: PTGDR-1 and/or PTGDR-2 antagonists for preventing and/or treating systemic lupus erythematosus
    Article Snippet: Mouse IL4 and IL1β ELISA kits were from BioLegend (San Diego, CA). .. Mouse IgE Quantification ELISA kits were from Bethyl Laboratories (Montgomery, TX). ..

    Conjugation Assay:

    Article Title: Eosinophil-derived interleukin-24 compromises epithelial integrity and aggravates airway remodeling in mouse models of allergic asthma
    Article Snippet: .. Information of antibodies used in this study Antigen Conjugation Clone #Catalog Dilution Supplier CD45 APC/Cyanine7 30-F11 #103116 1:100 BioLegend CD3 PerCP/Cyanine5.5 17A2 #100328 1:100 BioLegend B220 PerCP/ Cyanine5.5 RA3-6B2 #103236 1:100 BioLegend I-A/I-E FITC 2G9 #553623 1:100 BD Biosciences CCR3 PE J073E5 #144506 1:100 BioLegend CD11c PE/Cyanine7 N418 #117318 1:100 BioLegend F4/80 Brilliant Violet 421 BM8 #123132 1:100 BioLegend IL-24 Alexa Fluor 647 / #ITA6752 1:200 G-Biosciences SiglecF Alexa Fluor 488 E50-2440 #567005 1:100 BD Biosciences BrdU Alexa Fluor 488 3D4 #364106 1:100 BioLegend CD16/CD32 Unconjugated 2.4G2 #553142 1:100 BD Biosciences IgE Unconjugated / #A90-115B 1:10000 Bethyl Laboratories ZO-1 Unconjugated / #ab59720 1:50 Abcam MUC5AC Unconjugated 45M1 #ab3649 1:200 Abcam αSMA Unconjugated 1A4 #ab7817 1:1000 (IHC) 1:5000 (WB) Abcam IL-24 (for WB) Unconjugated 303308 #MA5-24013 1:1000 Invitrogen E-cadherin Unconjugated 67A4 #sc-21791 1:2000 Santa Cruz Vimentin Unconjugated RV202 #sc-32322 1:8000 Santa Cruz Slug Unconjugated A-7 #sc-166476 1:2000 Santa Cruz Snail Unconjugated E-10 #sc393172 1:2000 Santa Cruz GAPDH Unconjugated / #GTX100118 1:10000 GeneTex ..

    Immunohistochemistry:

    Article Title: Eosinophil-derived interleukin-24 compromises epithelial integrity and aggravates airway remodeling in mouse models of allergic asthma
    Article Snippet: .. Information of antibodies used in this study Antigen Conjugation Clone #Catalog Dilution Supplier CD45 APC/Cyanine7 30-F11 #103116 1:100 BioLegend CD3 PerCP/Cyanine5.5 17A2 #100328 1:100 BioLegend B220 PerCP/ Cyanine5.5 RA3-6B2 #103236 1:100 BioLegend I-A/I-E FITC 2G9 #553623 1:100 BD Biosciences CCR3 PE J073E5 #144506 1:100 BioLegend CD11c PE/Cyanine7 N418 #117318 1:100 BioLegend F4/80 Brilliant Violet 421 BM8 #123132 1:100 BioLegend IL-24 Alexa Fluor 647 / #ITA6752 1:200 G-Biosciences SiglecF Alexa Fluor 488 E50-2440 #567005 1:100 BD Biosciences BrdU Alexa Fluor 488 3D4 #364106 1:100 BioLegend CD16/CD32 Unconjugated 2.4G2 #553142 1:100 BD Biosciences IgE Unconjugated / #A90-115B 1:10000 Bethyl Laboratories ZO-1 Unconjugated / #ab59720 1:50 Abcam MUC5AC Unconjugated 45M1 #ab3649 1:200 Abcam αSMA Unconjugated 1A4 #ab7817 1:1000 (IHC) 1:5000 (WB) Abcam IL-24 (for WB) Unconjugated 303308 #MA5-24013 1:1000 Invitrogen E-cadherin Unconjugated 67A4 #sc-21791 1:2000 Santa Cruz Vimentin Unconjugated RV202 #sc-32322 1:8000 Santa Cruz Slug Unconjugated A-7 #sc-166476 1:2000 Santa Cruz Snail Unconjugated E-10 #sc393172 1:2000 Santa Cruz GAPDH Unconjugated / #GTX100118 1:10000 GeneTex ..

    Western Blot:

    Article Title: Eosinophil-derived interleukin-24 compromises epithelial integrity and aggravates airway remodeling in mouse models of allergic asthma
    Article Snippet: .. Information of antibodies used in this study Antigen Conjugation Clone #Catalog Dilution Supplier CD45 APC/Cyanine7 30-F11 #103116 1:100 BioLegend CD3 PerCP/Cyanine5.5 17A2 #100328 1:100 BioLegend B220 PerCP/ Cyanine5.5 RA3-6B2 #103236 1:100 BioLegend I-A/I-E FITC 2G9 #553623 1:100 BD Biosciences CCR3 PE J073E5 #144506 1:100 BioLegend CD11c PE/Cyanine7 N418 #117318 1:100 BioLegend F4/80 Brilliant Violet 421 BM8 #123132 1:100 BioLegend IL-24 Alexa Fluor 647 / #ITA6752 1:200 G-Biosciences SiglecF Alexa Fluor 488 E50-2440 #567005 1:100 BD Biosciences BrdU Alexa Fluor 488 3D4 #364106 1:100 BioLegend CD16/CD32 Unconjugated 2.4G2 #553142 1:100 BD Biosciences IgE Unconjugated / #A90-115B 1:10000 Bethyl Laboratories ZO-1 Unconjugated / #ab59720 1:50 Abcam MUC5AC Unconjugated 45M1 #ab3649 1:200 Abcam αSMA Unconjugated 1A4 #ab7817 1:1000 (IHC) 1:5000 (WB) Abcam IL-24 (for WB) Unconjugated 303308 #MA5-24013 1:1000 Invitrogen E-cadherin Unconjugated 67A4 #sc-21791 1:2000 Santa Cruz Vimentin Unconjugated RV202 #sc-32322 1:8000 Santa Cruz Slug Unconjugated A-7 #sc-166476 1:2000 Santa Cruz Snail Unconjugated E-10 #sc393172 1:2000 Santa Cruz GAPDH Unconjugated / #GTX100118 1:10000 GeneTex ..

    other:




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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