2021
DOI: 10.1016/j.aquaculture.2020.736027
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Development and characterization of novel cell lines from kidney and eye of rainbow trout, Oncorhynchus mykiss for virological studies

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Cited by 22 publications
(15 citation statements)
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“…GrB cells remained stable after 1-year storage in liquid nitrogen. Their viability was similar to that from other reported fish cell lines (Ou-Yang et al, 2010;Suryakodi et al, 2021).…”
Section: Discussionsupporting
confidence: 87%
“…GrB cells remained stable after 1-year storage in liquid nitrogen. Their viability was similar to that from other reported fish cell lines (Ou-Yang et al, 2010;Suryakodi et al, 2021).…”
Section: Discussionsupporting
confidence: 87%
“…In cell culture research, mycoplasma contamination is a serious problem since it affects cell growth, metabolic rate and chromosome number. In the present study, Hoechst 33258 stain was used to detect mycoplasma as reported by several investigators (Freiberg & Masover, 1990; Majeed et al., 2013; Suryakodi et al., 2021). No extranuclear fluorescence was observed in the established cell lines of snubnose pompano.…”
Section: Discussionmentioning
confidence: 93%
“…In the present study, the plating efficiency at the cell concentration of 1000 per flask was estimated to be about 64.22%, 53.46%, 61.24%, 58.23% and 68.42%, for the cell lines of SPG, SPH, SPK, SPE and SPF, respectively, whereas the plating efficiency was found to be less in all the cell lines at the seeding density of 100 cells per flask. High plating efficiency was observed in gill and fin cell lines of snubnose pompano as observed in kidney cell line of rainbow trout (Suryakodi et al, 2021), caudal fin cell line of T. tor (Yadav et al, 2012), SAF-1 cell line (Bejar et al, 1997) and GF-1 cells (Chi et al, 1999). an important factor since its use for various applications, especially gene expression studies to produce recombinant proteins, depends on it.…”
Section: Replication Efficiency Of Fnv and Tilvmentioning
confidence: 99%
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“…Appropriate amounts of the 30th passage SCC cells were harvested by trypsin digestion and the genomic DNA was extracted using the Cytogenome Extraction Kit (Tiangen, China) according to the manufacturer's instruction. Two pairs of primers were used to amplify the 16S rRNA and COI gene fragments of S. chuatsi (Palumbi et al, 1996; Suryakodi et al, 2021; Table 1). The PCR reaction mixture (25 μl) contained 12.5 μl of 2× Flash Hot Start MasterMix (Dye) (CoWin Biosciences, China), 1 μl each of primer pair (10 μmol/L), 1.5 μl of template DNA and 9 μl of sterile distilled H 2 O.…”
Section: Methodsmentioning
confidence: 99%