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Cloning of fowl adenovirus-4 DNA in a plasmid vector

机译:禽腺病毒4 DNA的质粒载体克隆

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The DNA was isolated from fowl adenovirus- 4 recovered in India and digested with restriction enzyme PstI and BamHI. The digested viral DNA was analyzed by 0.7% agarose gel electrophoresis. Digestion of FAV-4 DNA with PstI enzyme produced seven fragments of 17.38, 11.80, 4.62, 3.79, 3.27, 2.02 and 1.75 kb while digestion with BamHI gave eight fragments of 12.65, 11.22, 7.5 4.48, 3.35, 3.05, 1.92 and 1.75 kb sizes. Some bands were not visible in lower portion. The average size of FAV-4 DNA was 45 kb.The PstI and BamHI digested DNA fragments were cloned in pUC 18 cloning vector.
机译:从印度回收的禽腺病毒-4中分离出该DNA,并用限制酶PstI和BamHI消化。通过0.7%琼脂糖凝胶电泳分析消化的病毒DNA。用PstI酶消化FAV-4 DNA产生了七个片段,分别为17.38、11.80、4.62、3.79、3.27、2.02和1.75 kb,而用BamHI消化则得到了八个片段,分别为12.65、11.22、7.5 4.48、3.35、3.05、1.92和1.75 kb大小。一些带在下部不可见。 FAV-4 DNA的平均大小为45 kb。将PstI和BamHI消化的DNA片段克隆到pUC 18克隆载体中。

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