| Literature DB >> 31451107 |
Patrik Inderbitzin1,2, Marilena Christopoulou3, Dean Lavelle3, Sebastian Reyes-Chin-Wo3, Richard W Michelmore3,4, Krishna V Subbarao5, Ivan Simko6.
Abstract
Following publication of the original article [1], the author reported a processing error in Figure 5. This has been corrected in the original article.Entities:
Year: 2019 PMID: 31451107 PMCID: PMC6710860 DOI: 10.1186/s12870-019-1966-9
Source DB: PubMed Journal: BMC Plant Biol ISSN: 1471-2229 Impact factor: 4.215
Fig. 5LsVe1L specific PCR assay is allele-specific. Shown are results of LsVe1L-specific PCR assays with selected lettuce accessions with known LsVe genotypes and resistance phenotypes. Resistance (R) and susceptibility (S) is indicated by capital letters for each accession. In all cases, the outcomes of the PCR assays were as expected from genome sequencing. Amplicon sizes are indicated by > and correspond to 200 and 500 bp. Lane numbers are: 1. 2-log ladder, 2. cultivar Balady Banha (Ve genotype: LsVe1L, LsVe3L, LsVe4L), 3. cultivar Lolla Rossa (LsVe1L, LsVe3L, LsVe4L), 4. cultivar Plymouth (LsVe1L, LsVe3L, LsVe4L), 5. cultivar Cobham Green (LsVe3L, LsVe4L, LsVe1S, LsVe2S), 6. cultivar Lee Tal (LsVe4L, LsVe1S, LsVe2S), 7. cultivar Margarita (LsVe4L, LsVe1S, LsVe2S), 8. cultivar Anuenue (LsVe2S, LsVe3S), 9. cultivar Blonde Lente a Monter (LsVe1S, LsVe2S, LsVe3S), 10. cultivar Primus (LsVe1S, LsVe2S, LsVe3S), 11. negative control, and 12. 2-log ladder. PCR conditions are described in Table 4