2021
DOI: 10.1016/j.fsiae.2021.100028
|View full text |Cite
|
Sign up to set email alerts
|

DNA Barcode as an effective tool in the identification of billfishes (Scombroidei, Teleostei) from exported specimens

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
0
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 13 publications
0
0
0
Order By: Relevance
“…The thermocycling conditions consisted of initial denaturation at 95℃ (2 min) followed by denaturation at 94℃ (30 cycles, 45 s), annealing at 49.7 -60℃ (45 s); elongation at 72℃ (1 min), and final extension at 72℃ (10 min) before termination of the reaction at 4℃ [9,15]. The FishF1 primer region is typically short enough to be easily amplified using this PCR method, and its sequencing is technically feasible and facilitates efficient DNA barcoding workflow [25].…”
Section: Extraction Pcr and Dna Sequencingmentioning
confidence: 99%
“…The thermocycling conditions consisted of initial denaturation at 95℃ (2 min) followed by denaturation at 94℃ (30 cycles, 45 s), annealing at 49.7 -60℃ (45 s); elongation at 72℃ (1 min), and final extension at 72℃ (10 min) before termination of the reaction at 4℃ [9,15]. The FishF1 primer region is typically short enough to be easily amplified using this PCR method, and its sequencing is technically feasible and facilitates efficient DNA barcoding workflow [25].…”
Section: Extraction Pcr and Dna Sequencingmentioning
confidence: 99%