PCR Protocols 1990
DOI: 10.1016/b978-0-12-372180-8.50005-6
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OPTIMIZATION OF PCRs

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Cited by 670 publications
(525 citation statements)
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“…All of the selected phylogenetic marker sequences were successfully used for phylogenetic reconstruction in previous studies (White et al . 1990; Taberlet et al . 1991; Mummenhoff et al .…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…All of the selected phylogenetic marker sequences were successfully used for phylogenetic reconstruction in previous studies (White et al . 1990; Taberlet et al . 1991; Mummenhoff et al .…”
Section: Methodsmentioning
confidence: 99%
“…Primer sequences, including the ones for the amplification of ITS (White et al . 1990; Mummenhoff et al . 1997), trnL (Taberlet et al .…”
Section: Methodsmentioning
confidence: 99%
“…DNA was quantified in the extracts by fluorometry (QuBit 3.0, Thermo Fisher Scientific, USA), with individual extracts ranging from 4.32 to 24.6 ng total DNA. The second internal transcribed spacer (ITS2) region of ribosomal DNA was amplified by polymerase chain reaction (PCR) using the fungi‐specific gITS7 forward primer (Ihrmark et al., 2012) and the general eukaryote ITS4 reverse primer (White, Bruns, Lee, & Taylor, 1990). The gITS7 primer included unique indexed tags for each sample to allow for multiplex sequencing.…”
Section: Methodsmentioning
confidence: 99%
“…The nuclear ribosomal ITS region (including ITS1, 5.8S rRNA,and ITS2), an approximately 600‐base‐pair region frequently used in species‐level systematics for fungi, was chosen as the target gene because it has been proposed as the standard barcode for fungi and has the highest probability of successful identification for the broadest range of fungi, with the most clearly defined barcode gap between inter‐ and intraspecific variations (Schoch et al., 2012). The ITS gene was amplified by polymerase chain reactions (PCRs) using the fungal primer set of ITS1 (5′‐ NNNNNNNNNN TCCGTAGGTGAACCTGCGG‐3′) and ITS4 (5′‐TCCTCCGCTTATTGATATGC‐3′) (White, Bruns, Lee, & Taylor, 1990), where NNNNNNNNNN represents the 10‐bp barcode designed for sample identification and the ITS primers were fused with the 454 pyrosequencing adapters. The PCRs were carried out in a 20‐μl reaction mixture containing 4 μl 5× FastPfu Buffer, 0.4 μl FastPfu polymerase, 2 μl 2.5 mmol/L dNTP mix (all from Beijing TransGen Biotech Co., Ltd., Beijing, China), 0.8 μl 5 μmol/L of each primer, and 10 ng of template DNA.…”
Section: Methodsmentioning
confidence: 99%