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Matrix Metalloprotein
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- Nu kopenMatrix Metalloproteinase Protocols, Clark, Young, Rowan, (EDT) 9781603272988-,
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eBay-objectnummer:335217319554
Specificaties
- Objectstaat
- Title
- Matrix Metalloproteinase Protocols: 622 (Methods in Molecular Bi
- ISBN
- 9781603272988
- Publication Year
- 2010
- Series
- Methods in Molecular Biology Ser.
- Type
- Textbook
- Format
- Hardcover
- Language
- English
- Publication Name
- Matrix Metalloproteinase Protocols
- Item Length
- 10in
- Publisher
- Humana Press
- Item Width
- 7in
- Item Weight
- 44.1 Oz
- Number of Pages
- Xii, 492 Pages
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Product Information
Since the discovery of a collagen-degrading protease in the tadpole tail in 1962, matrix metalloproteinase research has led to the discovery of more than twenty distinct vertebrate MMPs, along with a variety of homologues from diverse organisms such as the sea urchin, plants, insects, and nematode worms. Fully updating and adding to the popular first edition, Matrix Metalloproteinase Protocols, Second Edition includes a series of state-of-the-art techniques provided by eminent experts in the field. Beginning with a brief overview of the MMP arena, from how these enzymes fit into the larger degradome to what occurs when their expression and function in the mouse is modulated, the volume continues with sections on the expression and purification of MMPs and TIMPs, the detection of MMPs and TIMPs at both the protein and mRNA level, and our ability to assay MMP and TIMP activities in a wide variety of circumstances. Written in the highly successful Methods in Molecular Biology (TM) series format, chapters contain introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and notes on troubleshooting and avoiding known pitfalls. Comprehensive and cutting-edge, Matrix Metalloproteinase Protocols, Second Edition is an ideal source for many of the essential laboratory techniques for both novice and seasoned researchers alike collected in one convenient volume.
Product Identifiers
Publisher
Humana Press
ISBN-10
1603272984
ISBN-13
9781603272988
eBay Product ID (ePID)
102906405
Product Key Features
Publication Name
Matrix Metalloproteinase Protocols
Format
Hardcover
Language
English
Publication Year
2010
Series
Methods in Molecular Biology Ser.
Type
Textbook
Number of Pages
Xii, 492 Pages
Dimensions
Item Length
10in
Item Width
7in
Item Weight
44.1 Oz
Additional Product Features
Series Volume Number
622
Number of Volumes
1 Vol.
Lc Classification Number
Qd415-436
Edition Number
2
Reviews
Review of the first edition: "The editor, Ian M. Clark, has done an excellent job in putting together a collection of articles that span what is now a fairly wide field. ...the content and writing are of a high standard...In chapter 3, covering structural studies and contributed by Wolfram Bode and Klaus Maskos, the authors point out the absence of specific discussions of three-dimensional structures amongst the plethora of general reviews on MMPs and TIMPs. Their contribution expertly fills that void....Indeed the 'Notes' section, at the end of each chapter, is where the benefit of much, often hard-earned, experience is to be reaped and is a valuable addition in almost every case. The last two sections, between them, cover detection of MMp and TIMP expression at both RNA and protein levels, and actively assays. Hore, particular mention must be made of the chapter dealing with zymography and reverse zymography in which Susan Hawkes and coauthors have carefully explained this technique. Their use of figures with detailed interpretation is really excellent and alone could justify the purchase of this book for many labs....this book is recommended as a reference text for all labs engaged in MMP research. There is enough variety for established research labs to find some new methods, and, for newcomers to the field, it should make working with MMPs and their inhibitors a very straightforward prospect." - TRENDS in Cell Biology
Table of Content
MMPs and TIMPs: An Overview.- Metalloproteases and the Degradome.- Mouse Models of MMP and TIMP Function.- Expression and Purification of MMPs and TIMPs.- Expression of Recombinant MMP-28 in Mammalian Cells.- Expression of Recombinant Matrix Metalloproteinases in Escherichia coli.- Expression of Recombinant ADAMTS in Insect Cells.- Expression and Purification of Membrane-Type MMPs.- Refolding of TIMP-2 from Escherichia coli Inclusion Bodies.- Purification of MMPs and TIMPs.- Detection of MMPs and TIMPs.- Real-Time PCR Expression Profiling of MMPs and TIMPs.- Analysis of the Degradome with the CLIP-CHIP(tm) Microarray.- In Situ Hybridization for Metalloproteinases and Their Inhibitors.- Immunohistochemistry of MMPs and TIMPs.- Single Nucleotide Polymorphism Genotyping in MMP Genes: The 5? Nuclease Assay.- Assay of MMP and TIMP Activities.- Methods for Studying Activation of Matrix Metalloproteinases.- Assay of Matrix Metalloproteinases Against Matrix Substrates.- Zymography and Reverse Zymography for Detecting MMPs and TIMPs.- In Situ Zymography.- Near-Infrared Optical Proteolytic Beacons for In Vivo Imaging of Matrix Metalloproteinase Activity.- Neoepitope Antibodies Against MMP-Cleaved and Aggrecanase-Cleaved Aggrecan.- In Vitro Model of Cartilage Degradation.- Immunoassays for Collagenase-Mediated Cleavage of Type I and II Collagens.- Collagen Degradation Assays.- Analysis of MMP-Dependent Cell Migration and Invasion.- Using Fluorogenic Peptide Substrates to Assay Matrix Metalloproteinases.- Kinetic Analysis of the Inhibition of Matrix Metalloproteinases: Lessons from the Study of Tissue Inhibitors of Metalloproteinases.- Identification of Cellular MMP Substrates Using Quantitative Proteomics: Isotope-Coded Affinity Tags (ICAT) and Isobaric Tags for Relative andAbsolute Quantification (iTRAQ).- Mechanism-Based Profiling of MMPs.
Copyright Date
2010
Topic
Life Sciences / Molecular Biology, Life Sciences / Biochemistry
Lccn
2009-943297
Dewey Decimal
572/.6
Intended Audience
Scholarly & Professional
Dewey Edition
22
Illustrated
Yes
Genre
Non-Classifiable, Science
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