Da: Books From California, Simi Valley, CA, U.S.A.
EUR 12,83
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Aggiungi al carrellospiral_bound. Condizione: Good. Ex- library copy with stamps and stickers.
Da: Second Chance Books, Independence, OR, U.S.A.
EUR 13,17
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Aggiungi al carrelloSoft cover. Condizione: Very Good. Name on front cover. Book.
Da: Zubal-Books, Since 1961, Cleveland, OH, U.S.A.
EUR 14,23
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Aggiungi al carrelloCondizione: Good. 221 pp., paperback, plastic-comb binding, ex library else text clean and binding tight. - If you are reading this, this item is actually (physically) in our stock and ready for shipment once ordered. We are not bookjackers. Buyer is responsible for any additional duties, taxes, or fees required by recipient's country.
EUR 20,43
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Aggiungi al carrelloCondizione: Good. Used book that is in clean, average condition without any missing pages.
EUR 16,93
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Aggiungi al carrelloCondizione: New. pp. 236 1st Edition.
EUR 14,11
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Aggiungi al carrelloCondizione: New. pp. 236.
EUR 15,78
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Aggiungi al carrelloCondizione: New. pp. 236.
EUR 29,85
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Aggiungi al carrelloCondizione: 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.
EUR 29,85
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Aggiungi al carrelloCondizione: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.
EUR 31,17
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Aggiungi al carrelloCondizione: New. Brand New Original US Edition. Customer service! Satisfaction Guaranteed.
EUR 36,20
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Aggiungi al carrelloBrand new book. Fast ship. Please provide full street address as we are not able to ship to P O box address.
EUR 58,86
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Aggiungi al carrelloCondizione: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.
EUR 69,98
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Aggiungi al carrelloBrand new book. Fast ship. Please provide full street address as we are not able to ship to P O box address.
EUR 96,09
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Aggiungi al carrelloCondizione: New. SUPER FAST SHIPPING.
EUR 111,88
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Aggiungi al carrelloCondizione: New.
Editore: Humana Press Inc., Totowa, NJ, 2013
ISBN 10: 1489940383 ISBN 13: 9781489940384
Lingua: Inglese
Da: Grand Eagle Retail, Mason, OH, U.S.A.
EUR 114,21
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Aggiungi al carrelloPaperback. Condizione: new. Paperback. Advances in bioscience research usually arise as a result of the continu ing refinement of existing technologies. However, there are a number of occa sions v^rhere newly developed methodologies have a profound effect on nearly all areas of research. Frequently these are techniques that are elegantly simple in concept and require minimal technical manipulation. Two of these revolu tionary techniques are the focus ofPCR Sequencing Protocols. The first such technique is enzymatic chain termination sequencing developed by Sanger and his co-workers in Cambridge and reported in 1977. This essentially brought the possibility of deriving nucleotide sequence information in a very short time scale and has been widely accepted in many laboratories as a routine molecular biological research tool. Furthermore, it has not only led to the sequencing of many genes and gene fragments, but has also allowed the tech nical means of sequencing the human genome. The second technique that has found widespread acceptance in basic applied research and many routine applications is the polymerase chain reac tion. This technique, first reported in 1985 by MuUis and his colleagues, pro vides the means to amplify nucleic acid sequence, which immediately proved invaluable in nearly all fields of biological laboratory research. Here, as with enzymatic DNA sequencing, is a very simple concept that relies on minimal information to prepare short oligonucleotide primers that direct the synthesis of a specified fi-agment o f DNA in the presence of a thermostable DNA polymerase. Here, as with enzymatic DNA sequencing, is a very simple concept that relies on minimal information to prepare short oligonucleotide primers that direct the synthesis of a specified fi-agment o f DNA in the presence of a thermostable DNA polymerase. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
EUR 120,68
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Aggiungi al carrelloCondizione: As New. Unread book in perfect condition.
Da: Ria Christie Collections, Uxbridge, Regno Unito
EUR 111,03
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Aggiungi al carrelloCondizione: New. In.
EUR 23,43
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Aggiungi al carrelloCondizione: Sehr gut. Zustand: Sehr gut | Sprache: Englisch | Produktart: Bücher.
EUR 137,98
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Aggiungi al carrelloCondizione: New. pp. 238.
EUR 92,27
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Aggiungi al carrelloCondizione: New.
Da: Kennys Bookshop and Art Galleries Ltd., Galway, GY, Irlanda
EUR 143,81
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Aggiungi al carrelloCondizione: New. Editor(s): Rapley, Ralph. Series: Methods in Molecular Biology. Num Pages: 232 pages, 24 black & white illustrations, biography. BIC Classification: PSF. Category: (P) Professional & Vocational. Dimension: 230 x 151 x 14. Weight in Grams: 354. . 2013. 1996th Edition. Paperback. . . . .
EUR 150,12
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Aggiungi al carrelloPaperback. Condizione: Brand New. 236 pages. 9.10x6.00x0.60 inches. In Stock.
EUR 178,17
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Aggiungi al carrelloCondizione: New. Editor(s): Rapley, Ralph. Series: Methods in Molecular Biology. Num Pages: 232 pages, 24 black & white illustrations, biography. BIC Classification: PSF. Category: (P) Professional & Vocational. Dimension: 230 x 151 x 14. Weight in Grams: 354. . 2013. 1996th Edition. Paperback. . . . . Books ship from the US and Ireland.
Editore: Humana Press Inc., Totowa, NJ, 2013
ISBN 10: 1489940383 ISBN 13: 9781489940384
Lingua: Inglese
Da: AussieBookSeller, Truganina, VIC, Australia
EUR 186,48
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Aggiungi al carrelloPaperback. Condizione: new. Paperback. Advances in bioscience research usually arise as a result of the continu ing refinement of existing technologies. However, there are a number of occa sions v^rhere newly developed methodologies have a profound effect on nearly all areas of research. Frequently these are techniques that are elegantly simple in concept and require minimal technical manipulation. Two of these revolu tionary techniques are the focus ofPCR Sequencing Protocols. The first such technique is enzymatic chain termination sequencing developed by Sanger and his co-workers in Cambridge and reported in 1977. This essentially brought the possibility of deriving nucleotide sequence information in a very short time scale and has been widely accepted in many laboratories as a routine molecular biological research tool. Furthermore, it has not only led to the sequencing of many genes and gene fragments, but has also allowed the tech nical means of sequencing the human genome. The second technique that has found widespread acceptance in basic applied research and many routine applications is the polymerase chain reac tion. This technique, first reported in 1985 by MuUis and his colleagues, pro vides the means to amplify nucleic acid sequence, which immediately proved invaluable in nearly all fields of biological laboratory research. Here, as with enzymatic DNA sequencing, is a very simple concept that relies on minimal information to prepare short oligonucleotide primers that direct the synthesis of a specified fi-agment o f DNA in the presence of a thermostable DNA polymerase. Here, as with enzymatic DNA sequencing, is a very simple concept that relies on minimal information to prepare short oligonucleotide primers that direct the synthesis of a specified fi-agment o f DNA in the presence of a thermostable DNA polymerase. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.
EUR 114,71
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Aggiungi al carrelloSoft cover. Condizione: New. ISBN:9780896033443.
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germania
EUR 85,59
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Advances in bioscience research usually arise as a result of the continu ing refinement of existing technologies. However, there are a number of occa sions v^rhere newly developed methodologies have a profound effect on nearly all areas of research. Frequently these are techniques that are elegantly simple in concept and require minimal technical manipulation. Two of these revolu tionary techniques are the focus ofPCR Sequencing Protocols. The first such technique is enzymatic chain termination sequencing developed by Sanger and his co-workers in Cambridge and reported in 1977. This essentially brought the possibility of deriving nucleotide sequence information in a very short time scale and has been widely accepted in many laboratories as a routine molecular biological research tool. Furthermore, it has not only led to the sequencing of many genes and gene fragments, but has also allowed the tech nical means of sequencing the human genome. The second technique that has found widespread acceptance in basic applied research and many routine applications is the polymerase chain reac tion. This technique, first reported in 1985 by MuUis and his colleagues, pro vides the means to amplify nucleic acid sequence, which immediately proved invaluable in nearly all fields of biological laboratory research. Here, as with enzymatic DNA sequencing, is a very simple concept that relies on minimal information to prepare short oligonucleotide primers that direct the synthesis of a specified fi-agment o f DNA in the presence of a thermostable DNA polymerase. 236 pp. Englisch.
Da: Majestic Books, Hounslow, Regno Unito
EUR 144,69
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Aggiungi al carrelloCondizione: New. Print on Demand pp. 238 23:B&W 6 x 9 in or 229 x 152 mm Perfect Bound on White w/Gloss Lam.
Da: Biblios, Frankfurt am main, HESSE, Germania
EUR 148,24
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Aggiungi al carrelloCondizione: New. PRINT ON DEMAND pp. 238.
Editore: Humana Press, Humana Press Aug 2013, 2013
ISBN 10: 1489940383 ISBN 13: 9781489940384
Lingua: Inglese
Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germania
EUR 106,99
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Advances in bioscience research usually arise as a result of the continu ing refinement of existing technologies. However, there are a number of occa sions v^rhere newly developed methodologies have a profound effect on nearly all areas of research. Frequently these are techniques that are elegantly simple in concept and require minimal technical manipulation. Two of these revolu tionary techniques are the focus ofPCR Sequencing Protocols. The first such technique is enzymatic chain termination sequencing developed by Sanger and his co-workers in Cambridge and reported in 1977. This essentially brought the possibility of deriving nucleotide sequence information in a very short time scale and has been widely accepted in many laboratories as a routine molecular biological research tool. Furthermore, it has not only led to the sequencing of many genes and gene fragments, but has also allowed the tech nical means of sequencing the human genome. The second technique that has found widespread acceptance in basic applied research and many routine applications is the polymerase chain reac tion. This technique, first reported in 1985 by MuUis and his colleagues, pro vides the means to amplify nucleic acid sequence, which immediately proved invaluable in nearly all fields of biological laboratory research. Here, as with enzymatic DNA sequencing, is a very simple concept that relies on minimal information to prepare short oligonucleotide primers that direct the synthesis of a specified fi-agment o f DNA in the presence of a thermostable DNA polymerase.Humana Press in Springer Science + Business Media, Heidelberger Platz 3, 14197 Berlin 236 pp. Englisch.