2016
DOI: 10.1016/j.dci.2015.09.009
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The noa gene is functionally linked to the activation of the Toll/Imd signaling pathways in Bactrocera dorsalis (Hendel)

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Cited by 21 publications
(19 citation statements)
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“…The glass capillaries used for microinjection were made from 50 µl glass micropipettes using a Puller at heater level 60.4 (PC-10, Narishige, Japan). The injection conditions were set to a Pi of 570 hpa and a Ti of 0.2 s. A total of 200 nl of solution was injected into each B. dorsalis fly 34 .…”
Section: Methodsmentioning
confidence: 99%
“…The glass capillaries used for microinjection were made from 50 µl glass micropipettes using a Puller at heater level 60.4 (PC-10, Narishige, Japan). The injection conditions were set to a Pi of 570 hpa and a Ti of 0.2 s. A total of 200 nl of solution was injected into each B. dorsalis fly 34 .…”
Section: Methodsmentioning
confidence: 99%
“…Plasmids were transformed into Escherichia coli HT115 (DE3) competent cells and individual colonies were cultured at 37 °C in 500 ml of LB medium and induced to generate dsRNA with 0.4 mM isopropyl-D-thiogalactoside (IPTG). dsRNA was extracted from aliquots of bacteria with a recently described protocol3940.…”
Section: Methodsmentioning
confidence: 99%
“…Positive clones were cultured at 378C in 100 ml Lysogeny Broth (LB) medium containing 50 lg/ml kanamycin and induced to generate dsRNA by the addition of 0.4 mM isopropyl-Dthiogalactoside, after which the bacteria were cultured for an additional 4 h at 378C. dsRNA was extracted according to the method described by Timmons et al (2001) and Dong et al (2016).…”
Section: Preparation Of Bacterially Expressed Dsrnamentioning
confidence: 99%