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Titlebook: Matrix Metalloproteinase Protocols; Ian M. Clark Book 2010Latest edition Humana Press 2010 Escherichia coli.Microarray.Nucleotide.PCR.Prot

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31#
發(fā)表于 2025-3-27 00:29:58 | 只看該作者
32#
發(fā)表于 2025-3-27 02:32:59 | 只看該作者
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發(fā)表于 2025-3-27 08:50:59 | 只看該作者
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發(fā)表于 2025-3-27 10:34:24 | 只看該作者
Mouse Models of MMP and TIMP Functionis indeed performed by some family members. However, matrix degradation is possibly not the predominant function of these enzymes. Several studies have demonstrated that MMPs also act on a variety of non-matrix extracellular proteins, such as cytokines, chemokines, receptors, junctional proteins, an
35#
發(fā)表于 2025-3-27 14:34:48 | 只看該作者
Expression of Recombinant Matrix Metalloproteinases in ,matrix (ECM). The role that the MMPs play in normal and pathological conditions has long been of interest. The mechanisms by which the MMPs cleave the different components of the ECM have been examined extensively. Some of these studies have been made possible, in part, by the ability to express rec
36#
發(fā)表于 2025-3-27 21:39:26 | 只看該作者
37#
發(fā)表于 2025-3-27 22:17:58 | 只看該作者
Expression and Purification of Membrane-Type MMPsicellular proteolysis. Understanding the activity, regulation, and function of MT-MMPs would provide important insight for ongoing research in many diseases including cancer, fibrosis, and autoimmune diseases. In this chapter, we introduce the methods to express and purify recombinant MT-MMPs using
38#
發(fā)表于 2025-3-28 03:28:21 | 只看該作者
Refolding of TIMP-2 from , Inclusion Bodies provide the necessary post-translational modification apparatus to produce authentic TIMP but are comparatively slow and more expensive. This chapter describes the production of native TIMP-2 (both full-length and the N-terminal domain) from . by in vitro refolding. The technique allows high-level
39#
發(fā)表于 2025-3-28 10:02:23 | 只看該作者
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