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Mouse ige ready set go

Manufactured by Thermo Fisher Scientific

The Mouse IgE Ready-Set-Go is a quantitative ELISA kit designed to measure mouse immunoglobulin E (IgE) levels in biological samples.

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4 protocols using mouse ige ready set go

1

Quantification of Mouse Serum IgE

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From mice included in the phenotyping study, blood samples were collected via cardiac puncture. Sera were separated by centrifugation and frozen at –20 °C for subsequent analysis of total IgE. A standard colorimetric sandwich ELISA was performed according to manufacturer directions (Mouse IgE Ready-Set-Go!, eBioscience, San Diego, CA). The lower limit of sensitivity was 4 ng/ml.
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2

Quantification of Mouse Serum IgE

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From mice included in the phenotyping study, blood samples were collected via cardiac puncture. Sera were separated by centrifugation and frozen at –20 °C for subsequent analysis of total IgE. A standard colorimetric sandwich ELISA was performed according to manufacturer directions (Mouse IgE Ready-Set-Go!, eBioscience, San Diego, CA). The lower limit of sensitivity was 4 ng/ml.
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3

Evaluation of Serum IgE, IL-23, and IL-17 Levels

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The levels of serum-IgE were evaluated by using Mouse IgE Ready-Set-Go (eBioscience). The detection limit was 4 ng/ml and results were shown as ng/ml IgE. Concentration of IL-23 in LHG was measured with Mouse IL-23 DuoSet ELISA (R&D Systems). The limit of detection was 4 ng/ml and results were shown as ng/ml IL-23. Concentration of IL-17 in LHG was measured with Mouse IL-17 DuoSet ELISA (R&D Systems). The limit of detection was 4 ng/ml and results were shown as ng/ml IL-17.
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4

Evaluating IgE Response to DDAC

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To further evaluate type of hypersensitivity response induced by DDAC, IgE was evaluated following dermal exposure. Since we previously identified that exposure duration may influence the development of allergic responses (Shane et al., 2017 (link)), IgE levels in mice exposed to DDAC for 14-days were assessed at 28 days post initial exposure. Mice (n=5) were treated for 14-days with DDAC and rested for 14-days. Blood samples were collected via cardiac puncture and sera was then separated by centrifugation and frozen at −20°C for subsequent analysis. To quantify serum IgE levels a standard colorimetric sandwich ELISA was performed according to manufacturer directions (Mouse IgE Ready-Set-Go!, eBioscience). To determine local production of IgE the IgE+B220+ (IgE+ B-cells) population were analyzed by flow cytometry as previously described using IgE-FITC (R35–72) (BD Biosciences) (Shane et al., 2017 (link)).
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