Lingua: Inglese
Editore: Tokyo ; Berlin ; Heidelberg ; New York ; Barcelona ; Hong Kong ; London ; Milan ; Paris : Springer, 2002
ISBN 10: 4431703136 ISBN 13: 9784431703136
Da: books4less (Versandantiquariat Petra Gros GmbH & Co. KG), Welling, Germania
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Aggiungi al carrelloBroschiert. Condizione: Gut. 446 Seiten; Der Erhaltungszustand des hier angebotenen Werks ist trotz seiner Bibliotheksnutzung sehr sauber. Es befindet sich neben dem Rückenschild lediglich ein Bibliotheksstempel im Buch; ordnungsgemäß entwidmet. In ENGLISCHER Sprache. Sprache: Englisch Gewicht in Gramm: 750.
Da: Universitätsbuchhandlung Herta Hold GmbH, Berlin, Germania
EUR 16,00
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Aggiungi al carrelloXVI, 446 p. Softcover. Versand aus Deutschland / We dispatch from Germany via Air Mail. Einband bestoßen, daher Mängelexemplar gestempelt, sonst sehr guter Zustand. Imperfect copy due to slightly bumped cover, apart from this in very good condition. Stamped. Stamped. Springer lab manual. Sprache: Englisch.
Da: Ria Christie Collections, Uxbridge, Regno Unito
EUR 139,58
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Aggiungi al carrelloCondizione: New. In.
Da: Books Puddle, New York, NY, U.S.A.
Condizione: New. pp. 466.
Da: Revaluation Books, Exeter, Regno Unito
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Aggiungi al carrelloPaperback. Condizione: Brand New. 1st edition. 446 pages. 9.25x6.00x1.00 inches. In Stock.
Da: AHA-BUCH GmbH, Einbeck, Germania
EUR 143,31
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - I started insect cell culture work in 1962, when T. D. C. Grace reported the first establishment of invertebrate continuous cell lines. He obtained grow ing cells from pupal ovaries of the emperor gum moth, Antheraea euca lypti. At that time, I was trying to obtain growing cells from leafhoppers. Grace's method could not be applied directly to my culture because of the differences in species, the size of the insects, and the tissue to be cul tured. The vertebrate tissue culture methods gave me some ideas for pre paring cultures from leafhoppers, but those could not be used directly either. There were no textbooks and no manuals for invertebrate tissue culture, so I had to develop a method by myself. First, I considered what type and what size of vessels are suitable for insect tissue culture. Also, I had to look for suitable materials to construct the culture vessels. Sec ond, I had to examine various culture media, especially growth-promot ing substances, such as sera. Then I had to improve culture media by trial and error. The procedure to set up a primary culture was also a problem. How could I sterilize materials How could I remove tissues from a tiny insect How many tissues should I pool in order to set up one culture I had to find out the answers. Naturally, it took a lot of time.
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Aggiungi al carrelloPaperback. Condizione: Like New. Like New. book.
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germania
EUR 139,09
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -I started insect cell culture work in 1962, when T. D. C. Grace reported the first establishment of invertebrate continuous cell lines. He obtained grow ing cells from pupal ovaries of the emperor gum moth, Antheraea euca lypti. At that time, I was trying to obtain growing cells from leafhoppers. Grace's method could not be applied directly to my culture because of the differences in species, the size of the insects, and the tissue to be cul tured. The vertebrate tissue culture methods gave me some ideas for pre paring cultures from leafhoppers, but those could not be used directly either. There were no textbooks and no manuals for invertebrate tissue culture, so I had to develop a method by myself. First, I considered what type and what size of vessels are suitable for insect tissue culture. Also, I had to look for suitable materials to construct the culture vessels. Sec ond, I had to examine various culture media, especially growth-promot ing substances, such as sera. Then I had to improve culture media by trial and error. The procedure to set up a primary culture was also a problem. How could I sterilize materials How could I remove tissues from a tiny insect How many tissues should I pool in order to set up one culture I had to find out the answers. Naturally, it took a lot of time. 464 pp. Englisch.
Da: moluna, Greven, Germania
EUR 115,65
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Aggiungi al carrelloCondizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. With step-by-step protocols, it introduces methods to initiate tissue culture from invertebrates including, Polifera, Coelenterata, Plathelminthes, Nematoda, Annedlia, Mollusca, Echinodermata, and ProchordataThe Appendix lists established cell lines ava.
Da: Majestic Books, Hounslow, Regno Unito
EUR 193,81
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Aggiungi al carrelloCondizione: New. Print on Demand pp. 466 Illus.
Lingua: Inglese
Editore: Springer, Springer Feb 2002, 2002
ISBN 10: 4431703136 ISBN 13: 9784431703136
Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germania
EUR 139,09
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -I started insect cell culture work in 1962, when T. D. C. Grace reported the first establishment of invertebrate continuous cell lines. He obtained grow ing cells from pupal ovaries of the emperor gum moth, Antheraea euca lypti. At that time, I was trying to obtain growing cells from leafhoppers. Grace's method could not be applied directly to my culture because of the differences in species, the size of the insects, and the tissue to be cul tured. The vertebrate tissue culture methods gave me some ideas for pre paring cultures from leafhoppers, but those could not be used directly either. There were no textbooks and no manuals for invertebrate tissue culture, so I had to develop a method by myself. First, I considered what type and what size of vessels are suitable for insect tissue culture. Also, I had to look for suitable materials to construct the culture vessels. Sec ond, I had to examine various culture media, especially growth-promot ing substances, such as sera. Then I had to improve culture media by trial and error. The procedure to set up a primary culture was also a problem. How could I sterilize materials How could I remove tissues from a tiny insect How many tissues should I pool in order to set up one culture I had to find out the answers. Naturally, it took a lot of time.Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 464 pp. Englisch.
Da: Biblios, Frankfurt am main, HESSE, Germania
EUR 194,53
Quantità: 4 disponibili
Aggiungi al carrelloCondizione: New. PRINT ON DEMAND pp. 466.