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Titlebook: Chemokine Protocols; Amanda E. I. Proudfoot,Timothy N. C. Wells,Christi Book 2000 Humana Press 2000

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书目名称Chemokine Protocols
编辑Amanda E. I. Proudfoot,Timothy N. C. Wells,Christi
视频video
概述Includes supplementary material:
丛书名称Methods in Molecular Biology
图书封面Titlebook: Chemokine Protocols;  Amanda E. I. Proudfoot,Timothy N. C. Wells,Christi Book 2000 Humana Press 2000
描述The chemokines family of small proteins are involved in numerous b- logical processes ranging from hematopoiesis, angiogenesis, and basal l- kocyte trafficking to the extravasation and tissue infiltration of leukocytes in response to inflammatory agents, tissue damage, and bacterial or viral infection. Chemokines exert their effects through a family of seven G-protein coupled transmembrane receptors. Worldwide interest in the chemokine field surged dramatically early in 1996, with the finding that certain chemokine receptors were the elusive coreceptors, required along with CD4, for HIV infection. Today, though over 40 human chemokines have been described, the n- ber of chemokine receptors lags behind—only 17 human chemokine receptors have been identified so far. What has emerged over the years is that most chemokine receptors bind several distinct ligands, and indeed the majority of chemokines are able to bind to multiple chemokine receptors, explaining to some extent the apparent disparity in the numbers of chemokines and rec- tors. Yet in spite of the apparent redundancy in chemokine/chemokine rec- tor interactions, it is clear that in vivo, spatial, temporal, and indeed cell- a
出版日期Book 2000
版次1
doihttps://doi.org/10.1385/1592590586
isbn_softcover978-1-61737-151-6
isbn_ebook978-1-59259-058-2Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2000
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Chemokine Expression in Insect Cells,ay be predicted from deduced amino acid sequence, a rigorous proof of identity of a gene will require a demonstration of the appropriate biological activities of gene products. Thus, efficient expression of recombinant proteins of cloned genes is essential to obtain proteins sufficient for detailed
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Expression of Chemokines in the Periplasmic Space of E. coli,ations, in the case of RANTES, and with a yield of several hundred micrograms from a 1-L culture. Other expression systems that are generally used for the production of chemokines have several disadvantages. Bacterial expression in the cytoplasm of . (.,.) gives large yields, but sometimes leads to
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Synthesis of Chemokines,ning has resulted in an explosion in the number of new chemokines from 1995-1998. However, for studies of the protein, knowing the DNA sequence is only the first step. The chemokine must be generated and in its correctly processed and folded form, and then purified to homogeneity. Expression of the
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Identification of Novel Chemokines From Expressed Sequence Tag Databases,hree-dimensional subunit structure. The original members of the superfamily, Interleukin-8 and MCP-1 were purified over 10 years ago. Following on from these discoveries, many more of these proteins were identified because of their ability to selectively recruit and activate specific leukocyte popul
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Generation of Stable Cell Lines Expressing Chemokine Receptors, expressing specific chemokine receptors greatly facilitates chemokine receptor characterization, particularly in terms of ligand binding specificity, analysis of signal transduction pathways, and for diverse functional assays ranging from chemotaxis to HIV infection. The availability of stable cell
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