Assessment of the quantity and purity of DNA obtained from buccal cells under different storage methods

T. Cavallari, L. Arima, S. Moysés, S. J. Moysés, R. Werneck
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Abstract

Aim: This study aimed to verify the quantity and purity of DNA obtained from buccal cells under differentstorage conditions. Methods: Thirty students, between 18 and 23 years of age participated in the study. Three samples of genetic material were collected from each student (samples A, B, and C) through a mouth rinse with 5 mL of 3% glucose. The first phase of DNA extraction from sample A was carried out on the same day of sample collection, whereas samples B and C were stored in a refrigerator and a freezer, respectively, for 1 month before the first extraction phase. DNA extraction was performed with 10 M ammonium acetate and 1 mM EDTA. Sample purity was assessed by spectrophotometry. Statistical analyses were performed through descriptive analysis and analysis of variance ANOVA using the SPSS software, version 21.0. Results: the samples presented no statistically significant differences between the DNA quantity (p = 0.37) or quality (p = 0.16). Conclusion: the quantity and purity of DNA extraction from the three samples were satisfactory, and no differences in storage conditions were found. Uniterms: DNA. Mouth. Mucosa.
不同保存方法下口腔细胞DNA的数量和纯度评价
目的:验证不同保存条件下口腔细胞DNA的数量和纯度。方法:30名年龄在18 ~ 23岁的学生参与研究。通过含5毫升3%葡萄糖的漱口水,从每个学生身上收集了三个遗传物质样本(样本A、B和C)。A样品的第一阶段DNA提取在样品采集当天进行,而B样品和C样品在第一阶段提取前分别在冰箱和冰柜中保存1个月。DNA提取液为10 M乙酸铵和1 mM EDTA。用分光光度法测定样品纯度。采用SPSS 21.0版软件,通过描述性分析和方差方差分析进行统计分析。结果:样品的DNA数量(p = 0.37)和质量(p = 0.16)差异无统计学意义。结论:三种样品的DNA提取量和纯度均令人满意,且保存条件无差异。Uniterms: DNA。的嘴。粘膜。
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