Pustowoit Barbara (24 results)
- Hardcover
Seller: Biblios, frankfurt am main, HESSE, GermanyBiblios
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Condition: New. pp. 152.
- Softcover
Seller: Ria Christie Collections, Uxbridge, United KingdomRia Christie Collections
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Condition: New. In.
Quantitation of mRNA by Polymerase Chain Reaction: Nonradioactive PCR Methods (Springer Lab Manuals)
Köhler, Thomas; Laßner, Dirk; Rost, Anne-Katrin; Thamm, Barbara; Pustowoit, Barbara; Remke, Harald
- Softcover
Seller: Ria Christie Collections, Uxbridge, United KingdomRia Christie Collections
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- Softcover
Seller: Books Puddle, New York, NY, U.S.A.Books Puddle
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Condition: New. pp. 156.
Modern Applications of DNA Amplification Techniques: Problems and New Tools
Lassner, Dirk (Editor)/ Pustowoit, Barbara (Editor)/ Rolfs, Arndt (Editor)
- Softcover
Seller: Revaluation Books, Exeter, , United KingdomRevaluation Books
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Paperback. Condition: Brand New. 151 pages. 10.00x7.01x0.36 inches. In Stock.
- Hardcover
Seller: Romtrade Corp., STERLING HEIGHTS, MI, U.S.A.Romtrade Corp.
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Condition: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.
- Hardcover
Seller: Basi6 International, Irving, TX, U.S.A.Basi6 International
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Condition: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.
- Hardcover
Seller: Ria Christie Collections, Uxbridge, United KingdomRia Christie Collections
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Condition: New. In.
- Hardcover
Seller: Books Puddle, New York, NY, U.S.A.Books Puddle
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Condition: Used. pp. 152 1st Edition.
- Softcover
Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
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Taschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - In the ten years since the first publication on PCR (Saiki et al. , 1985), this in vitro method of nucleic acid replication and modification has grown to rival in popularity traditional microbiological, genetical und technical procedures for clonin…g, sequencing, gene detecting and related procedures. To date the PCR literature has emphasized six main areas of application: genetic mapping, detection of mutations, genetic polymorphism, transcriptional splicing and regulation, molecular virology and quantitative procedures. The overwhelming focus of quantification of DNA or RNA by PCR has been on human microbiology and oncological problems. The exquisite sensitivity of PCR gives this method the ability to detect extremely rare DNAs, mRNAs, mRNAs in small numbers of cells or in small amounts of tissue, and mRNAs expressed in mixed-cell populations. However, the exact and accurate quantification of specific nucleic acids in biological samples is in spite of numerous publications in that field still a general problem: during the peR process, an unknown initial number of target sequences are used as a template from which a large quantity of specific product can be obtained. Although the amount of product formed is easy to determine, it is difficult to deduce the initial copy number of the target molecule because the efficiency of the peR is largely unknown.
- Softcover
Seller: preigu, Osnabrück, Germanypreigu
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Taschenbuch. Condition: Neu. Modern Applications of DNA Amplification Techniques | Problems and New Tools | Dirk Lassner (u. a.) | Taschenbuch | viii | Englisch | 2012 | Springer | EAN 9781461374558 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[do…t]com | Anbieter: preigu.
- Hardcover
Seller: Majestic Books, Hounslow, , United KingdomMajestic Books
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US$ 135.57
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Condition: Used. pp. 152.
Modern Applications of DNA Amplification Techniques: Problems and New Tools
Lassner, Dirk (Editor)/ Pustowoit, Barbara (Editor)/ Rolfs, Arndt (Editor)
- Hardcover
Seller: Revaluation Books, Exeter, , United KingdomRevaluation Books
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US$ 161.75
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Hardcover. Condition: Brand New. 143 pages. 10.50x7.00x0.50 inches. In Stock.
- Hardcover
Seller: moluna, Greven, , Germanymoluna
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US$ 124.18
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Condition: New. PCR Quantification and Technical Aspects: Multiple Competitors for Single-Tube Quantification of HIV1 DNA T. Vener, et al. Quantitation of p53 Tumor Suppressor Gene Copy Number in Tumor DNA Samples by Competitive PCR in an ELISA-Format M. Hahn, et al. Sta.
- Hardcover
Seller: Mispah books, Redhill, SURRE, United KingdomMispah books
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US$ 185.05
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Hardcover. Condition: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.
- Hardcover
Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
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Buch. Condition: Neu. Neuware - PCR Quantification and Technical Aspects: Multiple Competitors for Single-Tube Quantification of HIV1 DNA; T. Vener, et al. Quantitation of p53 Tumor Suppressor Gene Copy Number in Tumor DNA Samples by Competitive PCR in an ELISA-Format; M. Hahn, et al. Standardisation of Messenger RNA Quantificat…ion Using an RTPCR Method Involving Coamplification with a Multi-Specific Internal Control; D. Shire, et al. Quantitative Analysis of Human DNA Sequences by Solid-Phase Minisequencing; A.C. Syvänen. Bioimage Analysers: Application for Ribozyme Kinetics; C.S. Vörtler, K. Birikh. First Approaches to Quantitate MDR1Messenger RNA by in cell PCR; D. Lassner, et al. Application of in situ-PCR for Detection of Intracellular mRNAs; V. Uhlmann, et al. Psoralen Biotin: A Novel Reagent for Non-Enzymatic and Specific Labeling of Nucleic Acid Probes and Oligonucleotides; R.L. Burghoff, et al. The Effect of Quantitative Ratio between Primer Pairs on PCR Products in Multi-Target Amplification; D. Bercovich, et al. PCR Quantification of Infectious Agents: Quantitation of Rubella Virus Genome by QPCR and Its Application to Resolution for Mechanism of Congenital Rubella Syndrome; S. Katow, S. Arai. Significance of the Detection of Rubella Virus RNA by Nested PCR in Prenatal Diagnostics of Viral Infections; B. Pustowoit. Quantitative Detection of Human Cytomegalovirus DNA in Cerebrospinal Fluid by Polymerase Chain Reaction; J.U. Vogel, B. Weber. Quality Control and External Quality Assessment Schemes for the Diagnostic Use of PCR in Microbiological Laboratories-European Trials on Hepatitis B Virus and Cytomegalovirus; J. Schirm. Suppliers of Specialist Items. Index.
- Softcover
- Print on Demand
Seller: Brook Bookstore On Demand, Napoli, NA, ItalyBrook Bookstore On Demand
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Condition: new. Questo è un articolo print on demand.
- Softcover
- Print on Demand
Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, , GermanyBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -In the ten years since the first publication on PCR (Saiki et al. , 1985), this in vitro method of nucleic acid replication and modification has grown to rival in popularity traditional microbiological, genetical und technical proce…dures for cloning, sequencing, gene detecting and related procedures. To date the PCR literature has emphasized six main areas of application: genetic mapping, detection of mutations, genetic polymorphism, transcriptional splicing and regulation, molecular virology and quantitative procedures. The overwhelming focus of quantification of DNA or RNA by PCR has been on human microbiology and oncological problems. The exquisite sensitivity of PCR gives this method the ability to detect extremely rare DNAs, mRNAs, mRNAs in small numbers of cells or in small amounts of tissue, and mRNAs expressed in mixed-cell populations. However, the exact and accurate quantification of specific nucleic acids in biological samples is in spite of numerous publications in that field still a general problem: during the peR process, an unknown initial number of target sequences are used as a template from which a large quantity of specific product can be obtained. Although the amount of product formed is easy to determine, it is difficult to deduce the initial copy number of the target molecule because the efficiency of the peR is largely unknown. 156 pp. Englisch.
- Softcover
- Print on Demand
Seller: Majestic Books, Hounslow, , United KingdomMajestic Books
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Condition: New. Print on Demand pp. 156 66:B&W 7 x 10 in or 254 x 178 mm Perfect Bound on White w/Gloss Lam.
- Softcover
- Print on Demand
Seller: Biblios, frankfurt am main, HESSE, GermanyBiblios
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US$ 91.33
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Condition: New. PRINT ON DEMAND pp. 156.
Quantitation of mRNA by Polymerase Chain Reaction
Thomas Köhler|Dirk Laßner|Anne-Katrin Rost|Barbara Thamm|Barbara Pustowoit|Harald Remke
- Softcover
- Print on Demand
Seller: moluna, Greven, , Germanymoluna
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US$ 56.30
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Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. In this laboratory cook-book , the authors provide a concise guide to PCR-based techniques to quantify nucleic acids in biological and clinical samples using exclusively nonradioactive detection methods, e.g. HPLC, bi…otin and digoxigenin based protocols. E.
- Softcover
- Print on Demand
Seller: moluna, Greven, , Germanymoluna
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Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Proceedings of the Augustusburg Conference of Advanced Science on Problems of Quantitation of Nucleic Acids by Amplification Techniques held in Augustusburg, Germany, September 23-26, 1996 In the ten years since the f…irst publication on PCR (Saiki et .
- Softcover
- Print on Demand
Seller: buchversandmimpf2000, Emtmannsberg, BAYE, Germanybuchversandmimpf2000
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Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -In the ten years since the first publication on PCR (Saiki et al. , 1985), this in vitro method of nucleic acid replication and modification has grown to rival in popularity traditional microbiological, genetical und technical procedure…s for cloning, sequencing, gene detecting and related procedures. To date the PCR literature has emphasized six main areas of application: genetic mapping, detection of mutations, genetic polymorphism, transcriptional splicing and regulation, molecular virology and quantitative procedures. The overwhelming focus of quantification of DNA or RNA by PCR has been on human microbiology and oncological problems. The exquisite sensitivity of PCR gives this method the ability to detect extremely rare DNAs, mRNAs, mRNAs in small numbers of cells or in small amounts of tissue, and mRNAs expressed in mixed-cell populations. However, the exact and accurate quantification of specific nucleic acids in biological samples is in spite of numerous publications in that field still a general problem: during the peR process, an unknown initial number of target sequences are used as a template from which a large quantity of specific product can be obtained. Although the amount of product formed is easy to determine, it is difficult to deduce the initial copy number of the target molecule because the efficiency of the peR is largely unknown.Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 156 pp. Englisch.
- Hardcover
- Print on Demand
Seller: THE SAINT BOOKSTORE, Southport, , United KingdomTHE SAINT BOOKSTORE
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US$ 125.87
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Hardback. Condition: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.
