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Titlebook: Chemokine-Glycosaminoglycan Interactions; Methods and Protocol Alexandra R. Lucas Book 2023 The Editor(s) (if applicable) and The Author(s)

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樓主: Lipase
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發(fā)表于 2025-3-28 16:18:43 | 只看該作者
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發(fā)表于 2025-3-28 23:52:32 | 只看該作者
Remote Ischemic Pre-Conditioning (RIPC),issue protection. Myokines play a central role in repair, inflammatory, and immune responses after injury. Thus, the detailed protocol for RIPC might be useful for researchers to study mechanisms underlying RIPC-mediated tissue protection and crosstalk. Here, we describe a detailed RIPC protocol and show MG53 secretion after RIPC into the blood.
44#
發(fā)表于 2025-3-29 03:19:55 | 只看該作者
Ex Vivo Perfusion System to Analyze Chemokine-Driven Leukocyte Adhesion,ocytes and arteries isolated from different donors in one experiment, generating information on both vascular and leukocyte adhesive properties of both donors. This method provides a versatile, highly physiologically relevant model to investigate leukocyte adhesion.
45#
發(fā)表于 2025-3-29 08:58:24 | 只看該作者
In Vitro (Trans)Migration Experiment Using Chemokines as Stimulatory Factor,. The method described in this chapter intends to measure the migration of mouse T cells towards the chemoattractant CCL25, as a practical example of such (trans)migration experiment that can be further adopted to individual needs and requirements.
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發(fā)表于 2025-3-29 11:38:52 | 只看該作者
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發(fā)表于 2025-3-29 19:36:01 | 只看該作者
https://doi.org/10.1007/978-3-322-84927-4es and GAGs is an important factor affecting transplant rejection, and blocking the interactions between chemokines and GAGs can significantly reduce acute rejection after transplantation. Here, we investigated the interaction between chemokines and GAGs by establishing a mouse model of acute rejection after kidney transplantation.
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發(fā)表于 2025-3-29 21:02:06 | 只看該作者
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發(fā)表于 2025-3-30 03:55:30 | 只看該作者
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發(fā)表于 2025-3-30 06:31:08 | 只看該作者
Detection of Chemokine Binding Proteins Association to Cell Surface Glycosaminoglycans by Flow Cellthodology to evaluate the interaction of viral secreted proteins with cell-surface glycosaminoglycans by immunofluorescence and detection by flow cytometry or microscopy. These methods could be equally applied to other chemokine binding proteins that do not have viral origin.
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