• Toshiro Takai, Yuri Ochiai, Saori Ichikawa, Emi Sato, Takasuke Ogawa, Tomoko Tokura, Takatoshi Kuhara, Hiroshi Kawai, Hideki Hatanaka, Seizo Takahashi, Hideoki Ogawa, and Ko Okumura.
• Atopy (Allergy) Research Center, Juntendo University School of Medicine, Tokyo, Japan. t-takai@juntendo.ac.jp
• Allergol Int. 2009 Jun 1; 58 (2): 225-35.

BackgroundIn studies on allergies in mouse models, IgE production is an essential parameter to be evaluated. Here, we examine the effect of commercially available immunoreaction enhancer solutions and different blocking reagents in enzyme-linked immunosorbent assay (ELISA) for total or antigen-specific murine IgE in order to improve the assays.MethodsSera from mice immunized with recombinant house dust mite major allergens, Der f 1 and Der p 1, were used for the assays. Total IgE was measured by sandwich ELISA using monoclonal antibodies against murine IgE. Antigen-specific IgE was assayed using allergen-coated plates. Sensitivity or signal intensity in ELISA was compared among conditions differing in the use of enhancer solutions, blocking reagents, or monoclonal antibodies, and incubation time.ResultsUse of enhancer solutions improved the sensitivity of ELISA for total IgE by approximately 30-fold of that using a conventional buffer. A blocking reagent caused more unwanted enhancement of the background signal in blank wells in ELISA for total IgE compared with another blocking reagent, however, improved signal intensity in ELISA for antigen-specific ELISA without significant enhancement of the background signal. Optimal assay conditions were determined.ConclusionsEnhancer solutions are effective in improving ELISAs for total and antigen-specific murine IgE. Selection of blocking reagents was important to decrease unwanted enhancement of background signals and was effective in enhancing signals for positive samples. The ELISAs improved in this study are useful for the study of allergies in mouse models.

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