DNA提取
DNA
萃取(化学)
色谱法
聚合酶链反应
核酸
分子生物学
磷酸盐缓冲盐水
桑格测序
数字聚合酶链反应
荧光计
生物
化学
DNA测序
生物化学
荧光
基因
量子力学
物理
作者
Prachi Bapat,Sridhar Epari,Pradnya V Joshi,Dipika S Dhanavade,Rachna Rumde,Mamta Gurav,Omshree Shetty,Sangeeta Desai
摘要
Abstract Objectives Good-quality nucleic acid extraction from formalin-fixed, paraffin-embedded (FFPE) specimens remains a challenge in molecular-oncopathology practice. This study evaluates the efficacy of an in-house developed FFPE extraction buffer compared with other commercially available kits. Methods Eighty FFPE specimens processed in different surgical pathology laboratories formed the study sample. DNA extraction was performed using three commercial kits and the in-house developed FFPE extraction buffer. DNA yield was quantified by a NanoDrop spectrophotometer and Qubit Fluorometer, and its purity was measured by the 260/280-nm ratio. A fragment analyzer system was used for accurate sizing of DNA fragments of FFPE DNA. The downstream effects of all extraction methods were evaluated by polymerase chain reaction (PCR) and Sanger sequencing. Results In comparison with the commercial kits, the in-house buffer yielded higher DNA quantity and quality number (P < .0001). In addition, DNA integrity and fragment size were preserved in a significantly greater number of samples isolated with the in-house buffer (P < .05). The target PCR amplification rate with the in-house buffer extracted samples was also significantly higher, with 98% of the samples showing interpretable sequencing results. Conclusions The in-house developed FFPE extraction buffer performed superior to other methods in terms of suitability for downstream applications, time, cost-efficiency, and ease of performance.
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