Titlebook: c-di-GMP Signaling; Methods and Protocol Karin Sauer Book 2017 Springer Science+Business Media LLC 2017 Pseudomonas aeruginosa.FimA.HPLC.c-

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善辯

Applications and Usability of Interactive TVP-dependent motility, . represents a good model system to assess enzyme activity of diguanylate cyclases and phosphodiesterases using T4P-dependent motility as a readout. Here, we describe the assay, which allows correlating diguanylate cyclase and phosphodiesterase activity with T4P-dependent motility in ..

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Detection of Cyclic Dinucleotides by STING IRF3 (Interferon regulatory factor 3) for type I interferon production. Here, we describe some experimental procedures such as Isothermal Titration Calorimetry and luciferase reporter assays to study the CDNs binding and activity by STING proteins.

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Spectrophotometric and Mass Spectroscopic Methods for the Quantification and Kinetic Evaluation of Imetry (UPLC-MS/MS). These methods can be leveraged for a number of experimental applications including the evaluation of enzyme activity for the in vitro synthesis of c-di-GMP, examination of how molecular signals impact these activities, identifying the catalytic properties of hybrid DGC-PDE proteins, and the development of DGC inhibitors.

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Type IV Pili-Dependent Motility as a Tool to Determine the Activity of c-di-GMP Modulating Enzymes iP-dependent motility, . represents a good model system to assess enzyme activity of diguanylate cyclases and phosphodiesterases using T4P-dependent motility as a readout. Here, we describe the assay, which allows correlating diguanylate cyclase and phosphodiesterase activity with T4P-dependent motility in ..

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Zhuohua Liu,Wei Zhang,Chuankun Wuaphy (RP-HPLC) analysis has become a commonly used approach to accomplish these goals. The following describes the extraction and HPLC-based detection and quantification of c-di-GMP from . samples, a procedure that is amenable to modifications for the analysis of c-di-GMP in other bacterial species.

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Low-Data Complexity Attacks on Camelliantrations have been developed, they are time intensive, expensive, low-throughput, and incapable of directly monitoring dynamic changes in vivo. In this protocol, we provide a .-specific detailed methodology to assay the intracellular levels of cyclic di-GMP using biological reporters.

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