2013
DOI: 10.1007/s12041-013-0243-1
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The partial mitochondrial sequence of the Old World stingless bee, Tetragonula pagdeni

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Cited by 7 publications
(16 citation statements)
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“…As the typical mitogenome, it included 37 genes and one D-loop region, with these units distributed on both strands of the mitogenome (in detail see Table 1). It is worth mentioning that the order of these genes in our mitogenome is identical to the order in the partial mitogenome reported by Thummajitsakul et al (2013). As seen in other insects (Liu et al 2021), the mitochondrial genome of T. pagdeni has a substantially greater AT richness (76.77 %) than the GC value.…”
Section: General Mitogenome Featuressupporting
confidence: 82%
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“…As the typical mitogenome, it included 37 genes and one D-loop region, with these units distributed on both strands of the mitogenome (in detail see Table 1). It is worth mentioning that the order of these genes in our mitogenome is identical to the order in the partial mitogenome reported by Thummajitsakul et al (2013). As seen in other insects (Liu et al 2021), the mitochondrial genome of T. pagdeni has a substantially greater AT richness (76.77 %) than the GC value.…”
Section: General Mitogenome Featuressupporting
confidence: 82%
“…pagdeni mitogenome reported by Thummajitsakul et al . (2013) tthe lengths of them were 762 bp and 1,351 bp, respectively. The length difference of ribosomal RNA genes between the two T .…”
Section: Resultsmentioning
confidence: 99%
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“…The materials used in this study were a specimens of stingless bees species (five individuals/location), ethanol 96%, chloroform, isopropanol, TE buffer, CTAB 3%, DNA loading dye. The 16S rRNA DNA mitochondrial primer pairs employed in the study is LR13107-F as a forward primer: 5'-TGG CTG CAG TAT AAC TGA CTG TAC AAA GG-3' and LR12647-R as reverse primer: 5'-GAA ACC AAT CTG ACT TAC GTC GAT TTG A-3' (Thummajitsakul et al, 2013), PCR Kit (Go Taq Green©), Nuclease free water, DNA Ladder 1 kb and 100 bp, Promega Wizard sv gel© and PCR clean/up system kit©, 1% electrophoretic gel, TAE buffer, EtBr.…”
Section: Tools and Materialsmentioning
confidence: 99%
“…The amplification of Polymerase Chain Reaction (PCR) and DNA Sequencing was conducted using the mitochondrial 16S rRNA gene primers as described previously (Thummajitsakul et al, 2013). The PCR were completed in 35 cycles of 30 µl reaction volume, based on Na-Nokorn et al (2006) and Mahendran et al (2006).…”
Section: Dna Amplification and Sequencingmentioning
confidence: 99%