首页> 外文期刊>African Journal of Cellular Pathology >Effect of formalin fixation on DNA purity and quantity, nucleic acid, and amplicon size in cervical human papilloma virus detection
【24h】

Effect of formalin fixation on DNA purity and quantity, nucleic acid, and amplicon size in cervical human papilloma virus detection

机译:福尔马林固定对宫颈人乳头瘤病毒检测中DNA纯度和数量,核酸和扩增子大小的影响

获取原文
           

摘要

Tissue fixation with 10% formalin and molten paraffin wax embedding (FFPE) is routinely used protocol for tissue preservation in histopathology laboratory. We therefore aimed at comparing the differences in DNA quantity, DNA purity, nucleic acid and its effect on primers (PCR) amplicon (bp) sizes between fresh cervical tissues and formalin fixed paraffin embedded (FFPE). The differences in DNA purity, quantity and nucleic acid were 2.02±0.42 versus 1.34±0.28, 47.73±37.45 vs. 21.84±25.52 (ng/μl) and 1.56±0.59 vs 0.49±0.46 between for fresh cervical tissue and FFPE respectively and were all statistically significant at p<0.005. The difference in amplification successes was higher for the 120 bp than for the 450 bp primers. The distribution of cervical human papillomavirus for fresh tissues and formalin-fixed paraffin-embedded tissues studied was 39% and 13% respectively. Although, the present results showed that PCR genomic DNA can be extracted from both fresh cervical smear and 8 years duration FFPE archived tissue blocks. Formalin fixed paraffin embedded tissue blocks is not recommended for epidemiological study for detection and typing of cervical human papillomavirus using high molecular weight? base pair primers and conventional PCR.
机译:在组织病理学实验室中,通常使用10%福尔马林和熔融石蜡包埋法(FFPE)进行组织固定。因此,我们旨在比较新鲜宫颈组织和福尔马林固定石蜡包埋(FFPE)之间的DNA数量,DNA纯度,核酸及其对引物(PCR)扩增子(bp)大小的影响。新鲜宫颈组织和FFPE的DNA纯度,数量和核酸差异分别为2.02±0.42与1.34±0.28、47.73±37.45与21.84±25.52(ng /μl)和1.56±0.59与0.49±0.46之间,分别为均在p <0.005时具有统计学意义。 120 bp的扩增成功率差异高于450 bp的引物。宫颈人乳头瘤病毒在新鲜组织和福尔马林固定石蜡包埋的组织中的分布分别为39%和13%。虽然,目前的结果表明,可以从新鲜的宫颈涂片和8年的FFPE存档组织块中提取PCR基因组DNA。不建议将福尔马林固定的石蜡包埋的组织块用于流行病学研究中,以高分子量检测和分型宫颈人乳头瘤病毒。碱基对引物和常规PCR。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号