Kunzelmann Karl (53 results)

24 cm. 191 Seiten mit vielen farbigen Abbildungen. Pappband. Sehr gut. Sprache: deutsch. >>>Wichtige Zahlungs- / Versandinformationen:In Abweichung zu den automatisch angezeigten Versandkosten können leider bei einigen Büchern aufgrund des Formats oder Gewichts die angezeigten Versandkosten nicht eingehalten werden, da möglicherweise Paketversand erforderlich ist. Dadurch erhöhen sich die Versandkosten in diesen Fällen auf 6,50 bis 7,50 Euro. /// Aus Sicherheitsgründen,da desöfteren Postsendungen verschwinden bzw. der Verbleib nicht mehr nachverfolgbar ist, werden Sendungen ab einem Warenwert von 25 Euro nur als Einschreibebrief oder Paket verschickt. Die Versandkosten erhöhen sich dadurch auf 6,50 bis 7,00 Euro. /// Die Option Rechnung ist nur für bekannte Kunden möglich. Für alle anderen Besteller ist nur Lieferung nach Vorauszahlung möglich. /// Paypal kann nur bei Zahlungen aus dem Nicht-EU-Ausland ohne Zusatzkosten akzeptiert werden. Bei Paypal-Zahlungen aus Ländern innerhalb der EU wird die PayPal-Gebühr in Rechnung gestellt. Daher bitte nicht ohne vorherige Mitteilung (Vorausrechnung) zahlen. <<<.…

Condition: As New. Unread book in perfect condition.

Condition: New.

Condition: New. 2016. Paperback. . . . . .

Condition: New. In English.

Condition: As New. Unread book in perfect condition.

Condition: New.

Condition: New.

Condition: New.

Condition: New.

Condition: New. pp. 528.

Paperback. Condition: Brand New. reprint edition. 528 pages. 10.00x7.01x1.10 inches. In Stock.

Condition: New. 2016. Paperback. . . . . . Books ship from the US and Ireland.

Condition: New. In English.

Condition: New. In English.

Condition: As New. Unread book in perfect condition.

Condition: New. This volume details the cystic fibrosis transmembrane conductance regulator and its expression, biogenesis, structure and function in terms of the defects causing cystic fibrosis. It features readily reproducible laboratory protocols and troubleshooting tips. Editor(s): Amaral, Margarida D.; Kunzelmann, Karl. Series: Methods in Molecular Biology. Num Pages: 384 pages, 10 black & white tables, biography. BIC Classification: MBGL; MFGC; MFN. Category: (P) Professional & Vocational. Dimension: 262 x 185 x 27. Weight in Grams: 908. . 2011. 2011. Hardback. . . . . …

Condition: New. This volume details the cystic fibrosis transmembrane conductance regulator and its expression, biogenesis, structure and function in terms of the defects causing cystic fibrosis. It features readily reproducible laboratory protocols and troubleshooting tips. Editor(s): Amaral, Margarida D.; Kunzelmann, Karl. Series: Methods in Molecular Biology. Num Pages: 528 pages, 72 black & white illustrations, 4 colour illustrations, 15 black & white tables, biograph. BIC Classification: MBGL; MFGC; MFN. Category: (P) Professional & Vocational. Dimension: 260 x 186 x 34. Weight in Grams: 1158. . 2011. 2011th Edition. hardcover. . . . . …

Condition: Sehr gut. Zustand: Sehr gut | Seiten: 544 | Sprache: Englisch | Produktart: Bücher | Despite the many milestones in cystic fibrosis (CF) research, progress towards curing the disease has been slow, and it is increasingly difficult to grasp and use the already wide and still growing range of diverse methods currently employed to study CF so as to understand it in its multidisciplinary nature.  Cystic Fibrosis: Diagnosis and Protocols aims to provide the CF research community and related researchers with a very wide range of high-quality experimental tools, as an easy way to grasp and use classical and novel methods applied to cystic fibrosis.  Volume I: Approaches to Study and Correct CFTR Defects focuses on the cystic fibrosis transmembrane conductance regulator (CFTR) and its expression, biogenesis, structure, and function in terms of the defects causing CF.  Written in the highly successful Methods in Molecular Biology¿ series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.  Comprehensive and practical, Cystic Fibrosis: Diagnosis and Protocols will provide readers with optimal working tools to address pressing questions in the best technical way, while helping all of us, as a research and clinical community, to move faster hand-in-hand toward unravelling the secrets of this challenging disorder and cure it.…

Condition: Sehr gut. Zustand: Sehr gut | Seiten: 400 | Sprache: Englisch | Produktart: Bücher | Despite the many milestones in cystic fibrosis (CF) research, progress toward curing the disease has been slow, and it is increasingly difficult to grasp and use the already wide and still growing range of diverse methods currently employed to study CF so as to understand it in its multidisciplinary nature.  Cystic Fibrosis: Diagnosis and Protocols aims to provide the CF research community and related researchers with a very wide range of high-quality experimental tools, as an easy way to grasp and use classical and novel methods applied to cystic fibrosis.  Volume II: Methods and Resources to Understand Cystic Fibrosis focuses on pathophysiology, Omics approaches, and a variety of key resources recently made available for CF research.  Written in the highly successful Methods in Molecular Biology¿ series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.  Comprehensive and practical, Cystic Fibrosis: Diagnosis and Protocols will provide readers with optimal working tools to address pressing questions in the best technical way, while helping all of us, as a research and clinical community, to move faster hand-in-hand toward unravelling the secrets of this challenging disorder and cure it.…

Condition: New. pp. 400.

Condition: New. pp. 546.

Hardcover. Condition: Brand New. 1st edition. 384 pages. 10.00x7.00x1.25 inches. In Stock.

Condition: New. This volume details the cystic fibrosis transmembrane conductance regulator and its expression, biogenesis, structure and function in terms of the defects causing cystic fibrosis. It features readily reproducible laboratory protocols and troubleshooting tips. Editor(s): Amaral, Margarida D.; Kunzelmann, Karl. Series: Methods in Molecular Biology. Num Pages: 384 pages, 10 black & white tables, biography. BIC Classification: MBGL; MFGC; MFN. Category: (P) Professional & Vocational. Dimension: 262 x 185 x 27. Weight in Grams: 908. . 2011. 2011. Hardback. . . . . Books ship from the US and Ireland. …

Hardcover. Condition: Brand New. 544 pages. 10.25x7.00x1.25 inches. In Stock.

Condition: New. This volume details the cystic fibrosis transmembrane conductance regulator and its expression, biogenesis, structure and function in terms of the defects causing cystic fibrosis. It features readily reproducible laboratory protocols and troubleshooting tips. Editor(s): Amaral, Margarida D.; Kunzelmann, Karl. Series: Methods in Molecular Biology. Num Pages: 528 pages, 72 black & white illustrations, 4 colour illustrations, 15 black & white tables, biograph. BIC Classification: MBGL; MFGC; MFN. Category: (P) Professional & Vocational. Dimension: 260 x 186 x 34. Weight in Grams: 1158. . 2011. 2011th Edition. hardcover. . . . . Books ship from the US and Ireland. …

Paperback. Condition: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Condition: As New. Unread book in perfect condition.

Hardcover. Condition: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Condition: As New. Unread book in perfect condition.