Download Biotechnology and Genetics in Fisheries and Aquaculture, by Andy Beaumont, Pierre Boudry, Kathrin Hoare(auth.) PDF

By Andy Beaumont, Pierre Boudry, Kathrin Hoare(auth.)

Following the super well-received constitution of the 1st variation, this conscientiously revised and up to date new version now comprises a lot new info of important value to these operating and gaining knowledge of within the fisheries and aquaculture industries.

beginning with chapters overlaying genetic version and the way it may be measured, the authors then examine genetic constitution in ordinary populations, via a brand new bankruptcy protecting genetics with regards to inhabitants dimension and conservation concerns. Genetic version of features and triploids and the manipulation of ploidy are totally lined, and one other new bankruptcy is incorporated, entitled 'From Genetics to Genomics'. The ebook concludes with a bankruptcy overlaying the effect of genetic engineering in aquaculture.

With the inclusion of a wealth of up to date details, new textual content and figures and the inclusion of a 3rd writer, Pierre Boudry, the second one variation of Biotechnology and Genetics in Fisheries and Aquaculture offers a very good textual content and reference of significant worth and use to top point scholars and execs operating throughout fish biology, aquatic sciences, fisheries, aquaculture, genetics and biotechnology. Libraries in all universities and study institutions the place organic sciences, fisheries and aquaculture are studied and taught must have a number of copies of this glorious new version on their cabinets.

  • Completely up to date, revised and accelerated re-creation
  • Subject zone of ever expanding value
  • Expanded authorship
  • Commercially invaluable info for fish breeders

Content:
Chapter 1 what's Genetic edition? (pages 1–18):
Chapter 2 How can Genetic version be Measured? (pages 19–48):
Chapter three Genetic constitution in common Populations (pages 49–76):
Chapter four Genetics of inhabitants measurement in Conservation and Aquaculture (pages 77–97):
Chapter five Genetic edition of qualities (pages 99–128):
Chapter 6 From Genetics to Genomics (pages 129–143):
Chapter 7 Triploids and past: Why manage Ploidy? (pages 145–160):
Chapter eight Genetic Engineering in Aquaculture (pages 161–180):

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Extra info for Biotechnology and Genetics in Fisheries and Aquaculture, Second Edition

Example text

P1: IFM/UKS BLBK242-02 P2: SFK BLBK242-Beaumont January 4, 2010 23:20 Printer Name: Yet to Come How can genetic variation be measured? 29 Various standards can be run on gels alongside samples for comparison. Dyes and samples from individuals of known genotypes are run on protein and enzyme gels, while DNA bands of known sizes (in base pairs, bp, or kilobases, kb) are used as molecular size standards in DNA mini-gel or sequencing electrophoresis. 3c Slab gel DNA sequencer showing the upper and lower buffer trays.

From this point on, the number of newly synthesised molecules of the precise length specified by the two primers increases exponentially at each new cycle. 2b). P1: IFM/UKS BLBK242-02 P2: SFK BLBK242-Beaumont January 4, 2010 23:20 Printer Name: Yet to Come How can genetic variation be measured? We start with one strand of the template DNA on which are the forward and reverse primer sites: 3′ 5′ forward and reverse primer annealing sites CYCLE 1 The forward primer anneals to one end of the target stretch and is elongated in the 5' to 3' direction by DNA polymerase: 5′ 3′ 5′ 3′ forward primer polymerisation So, at the end of the first cycle there is the original template DNA plus what we will call an ‘overextended fragment’: 3′ template strand overextended fragment 5′ 5′ 3′ One such overextended fragment is produced every cycle for each DNA strand, so that if we run PCR for, say, 35 cycles there will be 35 such overextended fragments per original template strand.

The cut is uneven, producing an overlap on each end making them ‘sticky’ or ‘cohesive’. 1). 1 Recognition sequences and type of end sequence of three commonly used restriction endonucleases. Restriction endonuclease Recognition sequence End sequences EcoRI 5 –GAATTC–3 3 –CTTAAG–5 5 –AGCT–3 3 –TCGA–5 5 –GANTC–3 3 –CTNAG–5 5 –G 3 –CTTAA 5 –AG 3 –TC 5 –G 3 –CTNA AluI HinfI G, guanine; A, adenine; C, cytosine; T, thymine; N, any nucleotide. Type of end AATTC–3 G–5 CT–3 GA–5 ANTC–3 G–5 Sticky Blunt Sticky P1: IFM/UKS BLBK242-02 P2: SFK BLBK242-Beaumont January 4, 2010 23:20 Printer Name: Yet to Come How can genetic variation be measured?

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