Selected article for: "amplification reaction and dna detection"

Author: Baldwin, Don A.; Feldman, Michael; Alwine, James C.; Robertson, Erle S.
Title: Metagenomic Assay for Identification of Microbial Pathogens in Tumor Tissues
  • Document date: 2014_9_16
  • ID: xlqdn0c7_37
    Snippet: HPV16 PCR and capture sequencing. PCR amplification reaction mixtures for HPV16 detection contained 100 ng of tumor DNA and primer f1 (5= AAGCGAAGACAGCGGGTATG), f2 (5= AGGAGTACCTA CGACATGGGG), r1 (5= TGGTGTTTGGCATATAGTGTGTC), r2 (5= TGGCGTGTCTCCATACACTT), r3 (5= GTGGTGGGTGTAGCTTTTC GT), or r4 (5= TGGCAAGCAGGAAACGTACA). DNA was denatured at 94°C for 2 min, followed by 30 cycles of 94°C for 30 s, 57°C for 60 s, and 65°C for 60 s......
    Document: HPV16 PCR and capture sequencing. PCR amplification reaction mixtures for HPV16 detection contained 100 ng of tumor DNA and primer f1 (5= AAGCGAAGACAGCGGGTATG), f2 (5= AGGAGTACCTA CGACATGGGG), r1 (5= TGGTGTTTGGCATATAGTGTGTC), r2 (5= TGGCGTGTCTCCATACACTT), r3 (5= GTGGTGGGTGTAGCTTTTC GT), or r4 (5= TGGCAAGCAGGAAACGTACA). DNA was denatured at 94°C for 2 min, followed by 30 cycles of 94°C for 30 s, 57°C for 60 s, and 65°C for 60 s.

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