2022
DOI: 10.1007/s12600-022-01029-8
|View full text |Cite
|
Sign up to set email alerts
|

Unveiling the occurrence of Melanaphis sorghi in Argentina following a major aphid outbreak

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
3
2

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(1 citation statement)
references
References 8 publications
0
1
0
Order By: Relevance
“…Nuclear gene translation elongation factor 1-alpha and 18S rDNA from the aphid samples were amplified using previously published primers. Translation elongation factor 1-alpha was amplified using EF6 (TGA CCA GGG TGG TTC AAT AC) and EF3 (GAA CGT GAA CGT GGT ATC AC) primers and generated a ∼1014-bp fragment (von Dohlen et al 2002, Balbi et al 2023). The 18S rDNA gene fragments were amplified from aphid samples using N18SF (TTA AGG TGA AAC CGC GAA AGG) and N18SR (ACT TTA ATA TAC GCT ATT GGA GCT GGA) primers (Wieczorek and Kajtoch 2011) that generated a PCR product about 550 bp.…”
Section: Methodsmentioning
confidence: 99%
“…Nuclear gene translation elongation factor 1-alpha and 18S rDNA from the aphid samples were amplified using previously published primers. Translation elongation factor 1-alpha was amplified using EF6 (TGA CCA GGG TGG TTC AAT AC) and EF3 (GAA CGT GAA CGT GGT ATC AC) primers and generated a ∼1014-bp fragment (von Dohlen et al 2002, Balbi et al 2023). The 18S rDNA gene fragments were amplified from aphid samples using N18SF (TTA AGG TGA AAC CGC GAA AGG) and N18SR (ACT TTA ATA TAC GCT ATT GGA GCT GGA) primers (Wieczorek and Kajtoch 2011) that generated a PCR product about 550 bp.…”
Section: Methodsmentioning
confidence: 99%