SRX011200: SSU rRNA Gene Archaea V6 amplification of sample: CMM_0016_2008_05_14
1 LS454 (454 GS FLX) run: 21,567 spots, 3.1M bases, 8Mb downloads
Design: Genomic Archaea DNA of the SSU rRNA gene V6 hypervariable region was amplified using forward primer 958F (AATTGGANTCAACGCCGG) and reverse primer 1046R (CGRCRGCCATGYACCWC). We generated PCR amplicons in triplicate 30 uL reaction volumes with an amplification cocktail containing 1.0 U Platinum Taq Hi-Fidelity Polymerase (Invitrogen, Carlsbad, CA), 1X Hi-Fidelity buffer, 200 uM dNTP PurePeak DNA polymerase Mix (Pierce Nucleic Acid Technologies, Milwaukee, WI), 1.5 mM MgSO4 and 0.2 uM of each primer. We added a total of 10 ng template DNA to each PCR reaction and ran a negative, no-template control for each primer pair. Amplification conditions described in Sogin et al., 2006 were modified as follows: the initial 94C, 3 minute denaturation step was followed by 30 cycles of 94C for 30s, 57C for 60s, and 72C for 90s before a final 10 minute extension at 72C. The triplicate PCR products were pooled after amplification, purified using a QIAquick PCR purification kit (Qiagen, Valencia, CA) and eluted in 12 uL of Qiagen buffer EB following the manufacturer's protocol. We assessed the quality, size and concentration of PCR products on a Bioanalyzer 2100 (Agilent, Palo Alto, CA) using a DNA 1000 Lab Chip.
Submitted by: Marine Biological Laboratory
Study:
Microbial mat metagenome ICM_CMMshow Abstracthide AbstractAnalysis of diversity of coastal microbial mats using 454 technology.
Sample:
Generic sample from marine metagenomeLibrary:
Name: Av6
Instrument: 454 GS FLX
Strategy: AMPLICON
Source: METAGENOMIC
Selection: PCR
Layout: SINGLE
Spot descriptor:
5 forward
Runs:
1 run, 21,567 spots, 3.1M bases, 8Mb