本研究從富含多糖和次生物質的黃芪干燥根提取高質量的基因組DNA,為今后黃芪遺傳多樣性、分子鑒定研究奠定基礎。
實驗步驟
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實驗結果
采用改良的CTAB法、高鹽低pH法、SDS法、苯酚法等多種提取液提取黃芪干燥根的基因組 DNA,結果表明,CTAB法和高鹽低pH法能得到高質量的基因組DNA。用這兩種方法提取多批黃芪干燥根,瓊脂糖凝膠電泳條帶清晰,降解較少,能有效的從黃芪干藥材中提取到高質量的基因組DNA。將DNA以引物5S進行PCR擴增,獲得清晰的條帶。
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