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Extraction of High Quality DNA from Seized Moroccan Cannabis Resin (Hashish)

机译:从摩洛哥大麻树脂(大麻)中提取高质量的DNA

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摘要

The extraction and purification of nucleic acids is the first step in most molecular biology analysis techniques. The objective of this work is to obtain highly purified nucleic acids derived from Cannabis sativa resin seizure in order to conduct a DNA typing method for the individualization of cannabis resin samples. To obtain highly purified nucleic acids from cannabis resin (Hashish) free from contaminants that cause inhibition of PCR reaction, we have tested two protocols: the CTAB protocol of Wagner and a CTAB protocol described by Somma (2004) adapted for difficult matrix. We obtained high quality genomic DNA from 8 cannabis resin seizures using the adapted protocol. DNA extracted by the Wagner CTAB protocol failed to give polymerase chain reaction (PCR) amplification of tetrahydrocannabinolic acid (THCA) synthase coding gene. However, the extracted DNA by the second protocol permits amplification of THCA synthase coding gene using different sets of primers as assessed by PCR. We describe here for the first time the possibility of DNA extraction from (Hashish) resin derived from Cannabis sativa. This allows the use of DNA molecular tests under special forensic circumstances.
机译:核酸的提取和纯化是大多数分子生物学分析技术的第一步。这项工作的目的是获得源自大麻树脂缉获品的高度纯化的核酸,以进行用于大麻树脂样品个体化的DNA分型方法。为了从大麻树脂(Hashish)中获得高度纯化的核酸,使其不含引起PCR反应抑制的污染物,我们测试了两种方案:Wagner的CTAB方案和Somma(2004)描述的适用于困难基质的CTAB方案。我们使用适应方案从8次大麻脂缉获中获得了高质量的基因组DNA。通过Wagner CTAB协议提取的DNA无法提供四氢大麻酚(THCA)合酶编码基因的聚合酶链反应(PCR)扩增。但是,通过第二方案提取的DNA允许使用PCR评估的不同引物组扩增THCA合酶编码基因。我们在这里首次描述了从大麻植物中提取的(大麻)树脂中提取DNA的可能性。这允许在特殊的法医情况下使用DNA分子测试。

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