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Preparation of plasmid DNA was performed utilizing a modified alkaline lysis protocol followed by purification through anion exchange column (Qiagen, Valencia, CA).
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The constructs were amplified in large-scale bacterial cultures from which the fragments were obtained by a modified alkaline lysis procedure and subsequent digestion with EcoRV.
Objective: To correlate sperm variables with sperm DNA fragmentation, as assessed by using a modified alkaline comet assay for sperm smears.
Large EBV plasmids were propagated in DH10B and isolated with a modified alkaline lysis protocol.
BAC DNA was isolated using a modified alkaline lysis method [23].
Template DNA was extracted using a modified alkaline lysis protocol.
BAC DNA was isolated using a modified alkaline lysis method [ 17].
Plasmid DNA isolation was conducted following a modified alkaline lysis protocol [ 27].
Plasmids were isolated and purified automatically by a modified alkaline lysis procedure.
BAC DNA was isolated using a modified alkaline lysis method followed by purification.
Plasmid DNA was isolated using either the QIAprep® Spin Miniprep Kit (Qiagen) or a modified alkaline lysis procedure [ 96].
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