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Titlebook: Animal Models of Allergic Disease; Methods and Protocol Kumi Nagamoto-Combs Book 2021 Springer Science+Business Media, LLC, part of Springe

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發(fā)表于 2025-3-23 10:21:44 | 只看該作者
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發(fā)表于 2025-3-23 16:42:48 | 只看該作者
Experimental Mouse Models of Ragweed- and Papain-Induced Allergic Conjunctivitis, of the allergic inflammation. Immunohistochemical staining and quantitative PCR are used to clarify spatiotemporal expression of proinflammatory molecules in the conjunctival tissue. Flow cytometric analysis of conjunctival tissue is used for the detection of innate lymphoid cell type 2 (ILC2) in the ocular surface tissues.
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發(fā)表于 2025-3-23 20:12:59 | 只看該作者
An Overview of Flow Cytometry: Its Principles and Applications in Allergic Disease Research,ndously, and now some has the capacity to analyze 30–50 or more parameters on a single cell. Here, we describe the basic principles involved in the mechanics and procedures of flow cytometry along with an insight into applications of flow cytometry techniques for biomedical and allergic disease research.
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發(fā)表于 2025-3-23 22:45:23 | 只看該作者
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發(fā)表于 2025-3-24 03:02:51 | 只看該作者
Book 2021 reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls..?Authoritative and cutting-edge,?.Animal Models of Allergic Disease: Methods and Protocols .aims to offer a comprehensive collection of protocols and experience-derived instructions to further allergic disease research.
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發(fā)表于 2025-3-24 10:24:48 | 只看該作者
P. M. Mohan,P. Dhivya,K. Narayanamurthyodel and contemplated according to the intended purpose of the study. This chapter reviews our current knowledge on the application of mouse models to food allergy research and the variables that may influence the successful development of each type of model.
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發(fā)表于 2025-3-24 13:50:57 | 只看該作者
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發(fā)表于 2025-3-24 20:13:47 | 只看該作者
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發(fā)表于 2025-3-24 23:10:44 | 只看該作者
Corrections to: Population Ecology,n paraffin-embedded lungs, as well as in cytospin preparations from the lung. These antibody staining techniques enable either colorimetric or fluorescence imaging of eosinophils or their granule proteins with the potential for additional antibodies to be added for detection of multiple molecules.
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