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Titlebook: Cytokine Protocols; Marc Ley Book 2004 Humana Press 2004

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书目名称Cytokine Protocols
编辑Marc Ley
视频video
概述Includes supplementary material:
丛书名称Methods in Molecular Biology
图书封面Titlebook: Cytokine Protocols;  Marc Ley Book 2004 Humana Press 2004
描述Because cytokines regulate many different bodily functions in living organisms, mainly at the level of cell-cell communications, there is great interest in understanding their mode of action. In Cytokine Protocols, established researchers, physicians, and clinicians present their best biochemical, cellular, and molecular techniques for unraveling and quantifying the events occurring between the initial contact of a cytokine at the membrane receptor and the eventual activation of gene transcription. Described in step-by-step detail to ensure successful experimental results, these protocols cover the large-scale generation and purification of plasmid DNA, the identification of DNA-protein interactions via the gel mobility shift assay, RNA-level phenomena, and the isolation and characterization of cytokines, cytokine-related proteins, and their interactions. The techniques used include the generation of transfectants, the immunohistochemical detection of cytokines in tissue sections, and optimized staining for cytoplasmic detection. Highlights include RT-PCR of small amounts of mRNA, in situ hybridization, biosensor analysis, measurement of biological activities and standardization, i
出版日期Book 2004
版次1
doihttps://doi.org/10.1385/1592596673
isbn_softcover978-1-61737-269-8
isbn_ebook978-1-59259-667-6Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2004
The information of publication is updating

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https://doi.org/10.1007/978-981-99-5724-8by the special construction of the competitor, which bears the same primer-binding regions as the target of interest, but the sequence in between is modified in such a way that amplification products derived from the competitor and the target can be differentiated.
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Anthropology, Theatre, and Developmentysis methodologies, techniques which can provide a reasonable level of kinetic and ther-modynamic rigor and can be applicable across the broad range of molecular forms that incorporate cytokine and receptor. One such methodology that has significant promise is optical biosensor kinetics analysis. Th
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Getting Excited About “Calm Technology”aining polypeptide sequences (.). SH2 domains are recruited to tyrosine-phosphorylated proteins in their normal physiological setting; however, short synthetic phosphopeptides derived from these cellular docking sites contain all of the necessary binding determinants to interact with SH2 domains. Th
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Identification of ,-Acting Factors by Electrophoretic Mobility Shift Assay, mobility shift assay. The overall principle behind this technique involves the use of a radiolabeled piece of DNA mixed with a nuclear protein extract. The protein-DNA complex has a higher molecular weight than the DNA alone resulting in a slower moving or “shifted” band on a nondenaturing polyacry
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Competitive RT-PCR to Quantify Small Amounts of mRNA,by the special construction of the competitor, which bears the same primer-binding regions as the target of interest, but the sequence in between is modified in such a way that amplification products derived from the competitor and the target can be differentiated.
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Biosensor Analysis of Receptor-Ligand Interactions,ysis methodologies, techniques which can provide a reasonable level of kinetic and ther-modynamic rigor and can be applicable across the broad range of molecular forms that incorporate cytokine and receptor. One such methodology that has significant promise is optical biosensor kinetics analysis. Th
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