<p>Primers on the top are the forward primers and primers on the bottom are the reverse primers.</p
<p>(A) partial COI, and (B) 28S D2–D4 sequences from uropodoid mites collected from bark beetles.</p
<p>List of primers used in the amplification and sequencing of the 18 S rDNA gene.</p
a<p>Vectors used for cloning.</p>b<p>Genome coordinates <a href="http://www.plosone.org/article/info...
<p>Positions of forward (right-pointing arrow) and reverse (left-pointing arrow) primers are shown o...
<p>(A) The location of the LAMP primers within the selected sequence is shown. Arrows indicate the d...
<p>Underlined red font indicates the nucleotide sequences of each reverse primer for different <i>Ve...
<p>Forward and reverse primers designed based on the DNA-sequence of contigs.</p
Summary- Molecular probes were designed to identify Meloidogyne species by hybridizing to unique sig...
<p>These plasmids were verified by DNA sequencing. Underlined nucleotides indicate the designated si...
Molecular probes were designed to identify Meloidogyne species by hybridizing to unique signature se...
Molecular probes were designed to identify Meloidogyne species by hybridizing to unique signature se...
<p>The PCR primers are listed in pairs, with the forward primer (F) listed first and the reverse pri...
<p>(F): forward primer, (R): reverse primer. MS: Microsatellites. FAM: primer labeled with FAM in 5’...
<p>The names and orientations of the primers correspond to <a href="http://www.plosone.org/article/i...
<p>For the nested PCR, the first row for each gene depicts the primers used in the first and second ...
<p>(A) partial COI, and (B) 28S D2–D4 sequences from uropodoid mites collected from bark beetles.</p
<p>List of primers used in the amplification and sequencing of the 18 S rDNA gene.</p
a<p>Vectors used for cloning.</p>b<p>Genome coordinates <a href="http://www.plosone.org/article/info...
<p>Positions of forward (right-pointing arrow) and reverse (left-pointing arrow) primers are shown o...
<p>(A) The location of the LAMP primers within the selected sequence is shown. Arrows indicate the d...
<p>Underlined red font indicates the nucleotide sequences of each reverse primer for different <i>Ve...
<p>Forward and reverse primers designed based on the DNA-sequence of contigs.</p
Summary- Molecular probes were designed to identify Meloidogyne species by hybridizing to unique sig...
<p>These plasmids were verified by DNA sequencing. Underlined nucleotides indicate the designated si...
Molecular probes were designed to identify Meloidogyne species by hybridizing to unique signature se...
Molecular probes were designed to identify Meloidogyne species by hybridizing to unique signature se...
<p>The PCR primers are listed in pairs, with the forward primer (F) listed first and the reverse pri...
<p>(F): forward primer, (R): reverse primer. MS: Microsatellites. FAM: primer labeled with FAM in 5’...
<p>The names and orientations of the primers correspond to <a href="http://www.plosone.org/article/i...
<p>For the nested PCR, the first row for each gene depicts the primers used in the first and second ...
<p>(A) partial COI, and (B) 28S D2–D4 sequences from uropodoid mites collected from bark beetles.</p
<p>List of primers used in the amplification and sequencing of the 18 S rDNA gene.</p
a<p>Vectors used for cloning.</p>b<p>Genome coordinates <a href="http://www.plosone.org/article/info...
DOI
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