qPCR detection of pRi T-DNA genes in Reg 11 and R1 progeny populations of <i>O</i>. <i>fruticosum</i>.

<p>A positive (strain used to obtain the Ri line) and negative control (original genotypes either used to obtain the Ri line or used as parent) per set of progenies tested in the same qPCR run was included. Values represent the quantification cycle (Cq) values per gene. Values of T-DNA genes in bold indicate positive amplification based on Cq and amplicon melting profile, NA = gene not present in pRi used.</p> <p>(DOCX)</p>

Publication Details

Journal
Figshare
Published
2024-09-19
DOI
https://doi.org/10.1371/journal.pone.0306905.s003
Primary Topic
Wheat and Barley Genetics and Pathology
Type
article
Field-Weighted Citation Impact
0.00
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article

qPCR detection of pRi T-DNA genes in Reg 11 and R1 progeny populations of O. fruticosum.

Figshare
Wheat and Barley Genetics and Pathology
article

qPCR detection of pRi T-DNA genes in Reg 11 and R1 progeny populations of O. fruticosum.

article en

Abstract

<p>A positive (strain used to obtain the Ri line) and negative control (original genotypes either used to obtain the Ri line or used as parent) per set of progenies tested in the same qPCR run was included. Values represent the quantification cycle (Cq) values per gene. Values of T-DNA genes in bold indicate positive amplification based on Cq and amplicon melting profile, NA = gene not present in pRi used.</p> <p>(DOCX)</p>

Figshare
Openalex Percentile: Top 32%
Wheat and Barley Genetics and Pathology
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qPCR detection of pRi T-DNA genes in Reg 11 and R1 progeny populations of <i>O</i>. <i>fruticosum</i>. · Figshare (2024) | TGRS Research Map | TGRS