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      Chapter

      2Chapter 1 Archaeal Diversity Analysis Using 16S rDNA T-RFLP (Terminal-Restriction Fragment Length Polymorphisms)
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      Chapter

      2Chapter 1 Archaeal Diversity Analysis Using 16S rDNA T-RFLP (Terminal-Restriction Fragment Length Polymorphisms)

      DOI link for 2Chapter 1 Archaeal Diversity Analysis Using 16S rDNA T-RFLP (Terminal-Restriction Fragment Length Polymorphisms)

      2Chapter 1 Archaeal Diversity Analysis Using 16S rDNA T-RFLP (Terminal-Restriction Fragment Length Polymorphisms) book

      2Chapter 1 Archaeal Diversity Analysis Using 16S rDNA T-RFLP (Terminal-Restriction Fragment Length Polymorphisms)

      DOI link for 2Chapter 1 Archaeal Diversity Analysis Using 16S rDNA T-RFLP (Terminal-Restriction Fragment Length Polymorphisms)

      2Chapter 1 Archaeal Diversity Analysis Using 16S rDNA T-RFLP (Terminal-Restriction Fragment Length Polymorphisms) book

      Edited ByRoberto Danovaro
      BookMethods for the Study of Deep-Sea Sediments, Their Functioning and Biodiversity

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      Edition 1st Edition
      First Published 2009
      Imprint CRC Press
      Pages 12
      eBook ISBN 9780429130960
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      ABSTRACT

      Water bath or thermal block Centrifuges (must be suitable for 2 mL test tubes and for 50 mL test tubes) Vortex Thermalcycler Transilluminator UV-VIS spectrophotometer Complete apparatus for horizontal electrophoresis (including casting trays, electrophoretic

      chamber, and power supply) ABI 310 or 3100 sequencer (if not available, the capillary electrophoresis of digests can be

      carried out by an external subcontractor) Microwave

      Wash Solution 1: 50 mM Tris-HCl, pH 8.3; 200 mM NaCl; 5 mM Na2EDTA; 0.05% Triton X-100

      Wash Solution 2: 50 mM Tris-HCl, pH 8.3; 200 mM NaCl; 5 mM Na2EDTA Wash Solution 3: 10 mM Tris-HCl, pH 8.3; 0.1 mM Na2EDTA

      Ultrapure water: Reagent-grade water, previously autoclaved, ltered (through 0.2 µm) and stored into sterile 2 mL Eppendorf tubes at 4°C or −20°C

      UltraClean™ Soil DNA Isolation Kit (MoBio, catalog #12800-100) MasterTaq® kit (Eppendorf AG, Germany) Agarose TBE 10× (can be purchased from BIORAD or similar, or, alternatively, prepared as follows

      (for 1 L): 108 g TRIS Base, 55 g Boric Acid, 40 mL EDTA 0.5M pH 8, reagent-grade water to volume)

      TBE 1×: dilute TBE 10× (100 mL TBE 10× + 900 mL of reagent-grade water) Ethidium Bromide (10 mg mL−1 in ultrapure water) Loading dye 6X (Promega, Fermentas, or similar) Molecular weight 100 bp (Fermentas or similar) Wizard® PCR cleanup system (Promega) Alu I restriction enzyme (Promega, Fermentas, or other) Formamide Internal size standard (GS1000ROX; Applied Biosystems)

      The application of the 16S rDNA gene T-RFLP method to sediment samples involves the following steps:

      1. DNA extraction and purication (with the aim of extracting genomic DNA from benthic microrganisms, which must be of sufcient purity to carry out subsequent PCR-based analyses).

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