ISBN: 9780896034686 - Protein Phosphatase Protocols: 93 (methods in Molecular Biology, 93) (20 results)

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  • Language: English

    Published by Humana, 1998

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    Condition: very_good. Gently read. May have name of previous ownership, or ex-library edition. Binding tight; spine straight and smooth, with no creasing; covers clean and crisp. Minimal signs of handling or shelving. 100% GUARANTEE! Shipped with delivery confirmation, if you're not satisfied with purchase please return item! Ships USPS Media Mail.…

  • Language: English

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    Condition: Used - Very Good. VG hardback. First Edition. Methods in Molecular Biology, 93. In glazed boards. Text clean; binding tight; a bright, tidy copy Used - Very Good. VG hardback.

  • Language: English

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  • Language: English

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  • Language: English

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    Condition: Used. pp. 336.

  • Language: English

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    Condition: Used. pp. 336 9:B&W 6 x 9 in or 229 x 152 mm Case Laminate on Creme w/Gloss Lam.

  • Language: English

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  • Language: English

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  • Language: English

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  • Language: English

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    Condition: New. This text provides techniques for investigating the structure and function of protein/threonine phosphatases. The techniques, all optimized for ease of reproducibility, serve to isolate, identify and assay phosphatase activities from prokaryotic and eukaryotic sources. Series: Methods in Molecular Biology. Num Pages: 316 pages, biography. BIC Classification: PSBC; PSD; PSF. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 235 x 155 x 22. Weight in Grams: 663. . 1998. Hardback. . . . . …

  • Language: English

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  • Language: English

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    Gebunden. Condition: New. A major mechanism by which cells regulate protein function is to place phosphate groups on serine and threonine residues. Though the steady-state level of protein phosphorylation depends on the relative activities of both kinases and phosphatases, a much gr.

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    Language: English

    Published by Humana Press, 1998

    0896034682 / 9780896034686

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    Buch. Condition: Neu. Protein Phosphatase Protocols | John W. Ludlow | Buch | xiii | Englisch | 1998 | Humana Press | EAN 9780896034686 | Verantwortliche Person für die EU: Humana Press in Springer Science + Business Media, Heidelberger Platz 3, 14197 Berlin, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.…

  • Language: English

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  • Language: English

    Published by Humana Press Inc., 1998

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    Condition: New. This text provides techniques for investigating the structure and function of protein/threonine phosphatases. The techniques, all optimized for ease of reproducibility, serve to isolate, identify and assay phosphatase activities from prokaryotic and eukaryotic sources. Series: Methods in Molecular Biology. Num Pages: 316 pages, biography. BIC Classification: PSBC; PSD; PSF. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 235 x 155 x 22. Weight in Grams: 663. . 1998. Hardback. . . . . Books ship from the US and Ireland. …

  • Language: English

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  • Language: English

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  • Language: English

    Published by Humana Press, 1998

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    Buch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - A major mechanism by which cells regulate protein function is to place phosphate groups on serine and threonine residues. Though the steady-state level of protein phosphorylation depends on the relative activities of both kinases and phosphatases, a much greater effort has previously gone into the study of the former that the latter . Today, however, there is an increasing appreciation for the role that protein phosphatases play in the dynamic p- cess of protein phosphorylation . To date, there are four major types of protein serine/threonine phosphatase catalytic subunits, designated protein phosphatase type 1, 2A, 2B, and 2C . Each has been identified by the techniques of protein chemistry and enzymology and can be distinguished from one another by their preference for specific substrates as well as their sensitivity to certain acti- tors and inhibitors . Protein Phosphatase Protocols has been assembled in response to the growing interest these enzymes are receiving . The goal of this compilation is to provide a 'how-to' experimental guide to aid newcomers as well as s- soned veterans in their research endeavors, thus further contributing towards our ever increasing knowledge of serine/threonine phosphatases . What you have before you contains contributions by many of the current and emerging leaders in the field . To highlight just a few, these chapters c- tain step-by-step information on how to isolate novel phosphatases and re- latory subunits, assay for activity, and generate immunological reagents for both biochemical and biological characterization of these enzymes .…

  • Language: English

    Published by Humana Press Mai 1998, 1998

    0896034682 / 9780896034686

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    Buch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -A major mechanism by which cells regulate protein function is to place phosphate groups on serine and threonine residues. Though the steady-state level of protein phosphorylation depends on the relative activities of both kinases and phosphatases, a much greater effort has previously gone into the study of the former that the latter . Today, however, there is an increasing appreciation for the role that protein phosphatases play in the dynamic p- cess of protein phosphorylation . To date, there are four major types of protein serine/threonine phosphatase catalytic subunits, designated protein phosphatase type 1, 2A, 2B, and 2C . Each has been identified by the techniques of protein chemistry and enzymology and can be distinguished from one another by their preference for specific substrates as well as their sensitivity to certain acti- tors and inhibitors . Protein Phosphatase Protocols has been assembled in response to the growing interest these enzymes are receiving . The goal of this compilation is to provide a 'how-to' experimental guide to aid newcomers as well as s- soned veterans in their research endeavors, thus further contributing towards our ever increasing knowledge of serine/threonine phosphatases . What you have before you contains contributions by many of the current and emerging leaders in the field . To highlight just a few, these chapters c- tain step-by-step information on how to isolate novel phosphatases and re- latory subunits, assay for activity, and generate immunological reagents for both biochemical and biological characterization of these enzymes . 336 pp. Englisch.…

  • Language: English

    Published by Humana Press, Humana Press Mai 1998, 1998

    0896034682 / 9780896034686

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    Buch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -A major mechanism by which cells regulate protein function is to place phosphate groups on serine and threonine residues. Though the steady-state level of protein phosphorylation depends on the relative activities of both kinases and phosphatases, a much greater effort has previously gone into the study of the former that the latter . Today, however, there is an increasing appreciation for the role that protein phosphatases play in the dynamic p- cess of protein phosphorylation . To date, there are four major types of protein serine/threonine phosphatase catalytic subunits, designated protein phosphatase type 1, 2A, 2B, and 2C . Each has been identified by the techniques of protein chemistry and enzymology and can be distinguished from one another by their preference for specific substrates as well as their sensitivity to certain acti- tors and inhibitors . Protein Phosphatase Protocols has been assembled in response to the growing interest these enzymes are receiving . The goal of this compilation is to provide a 'how-to' experimental guide to aid newcomers as well as s- soned veterans in their research endeavors, thus further contributing towards our ever increasing knowledge of serine/threonine phosphatases . What you have before you contains contributions by many of the current and emerging leaders in the field . To highlight just a few, these chapters c- tain step-by-step information on how to isolate novel phosphatases and re- latory subunits, assay for activity, and generate immunological reagents for both biochemical and biological characterization of these enzymes .Humana Press in Springer Science + Business Media, Heidelberger Platz 3, 14197 Berlin 336 pp. Englisch.…