1998
DOI: 10.1006/fstl.1997.0304
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Detection of Irradiated Fresh Chicken, Pork and Fish using the DNA Comet Assay

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Cited by 23 publications
(8 citation statements)
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“…For irradiated samples, intact cells were not seen in these samples, which suggest that the DNA comet assay could be used to discriminate visually irradiated ostrich meat from the nonirradiated controls at 1 kGy or more. Also, these results are in agreement with a report on DNA comet assay in irradiated fresh chicken, pork, and salmon (Cerda 1998a). Figure 2 shows significant differences in tail length (from the comet head to the end of the tail) between the control and 3 other irradiated samples.…”
Section: Dna Comet Assaysupporting
confidence: 94%
See 1 more Smart Citation
“…For irradiated samples, intact cells were not seen in these samples, which suggest that the DNA comet assay could be used to discriminate visually irradiated ostrich meat from the nonirradiated controls at 1 kGy or more. Also, these results are in agreement with a report on DNA comet assay in irradiated fresh chicken, pork, and salmon (Cerda 1998a). Figure 2 shows significant differences in tail length (from the comet head to the end of the tail) between the control and 3 other irradiated samples.…”
Section: Dna Comet Assaysupporting
confidence: 94%
“…However, the difference in comet length was not significant among the irradiated samples. Cerda (1998a) reported A, 0 kGy; B, 1 kGy; C, 3 kGy; D, 7 kGy). Silver staining: anode to the right.…”
Section: Dna Comet Assaymentioning
confidence: 96%
“…However, double strand DNA damage can also be observed in case the comet assay is used under neutral conditions [25]. For the analysis, the supernatant of testicular tissue homogenate was used [26]. All microscope slides were covered with a coat of agarose (0.5%, normal melting point) and dehydrated at room temperature.…”
Section: Comet Assaymentioning
confidence: 99%
“…For comet assay, a piece of the liver cut into thin slices were placed in phosphate buffered saline. Tissues were allowed to stir for dissociation at 500 rpm for 10 min to get the cell suspension [25] . For oxidative stress parameters, a homogenate from about 0.5 g of the remaining liver was obtained with a homogenizer (IKA Ultra-Turrax T10 basic model, Germany) in cold buffer solution of 140 mM KCl and 50 mM Tris-HCl (pH 7.6) for 2 min at 13000 rpm.…”
Section: Sample Preparationmentioning
confidence: 99%