A simple and practical method that prepares high molecular weight DNA ladders

Ethanol precipitation Multiple displacement amplification Restriction digest DNA clamp
DOI: 10.3892/mmr.2012.1061 Publication Date: 2012-09-04T12:05:49Z
ABSTRACT
The purpose of the current study was to report a simple and practical method prepare high molecular weight (mw) DNA ladders. involves 1,000-4,000-base pairs (bp) fragments being amplified by polymerase chain reaction (PCR), using λ as template. constructed plasmids are digested restriction endonucleases produce 5-, 6-, 8- 10-kb fragments, followed purification precipitation with ethanol, mixed proportionally. 1,000-4,000-bp were successfully generated PCR obtained through digestion plasmids. bands prepared mw ladder clear may aid future biology studies.
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