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Gel purification of gDNA for next-generation sequencing applications

Author(s)
Utthiya, Supanut
Wonnapinij, Passorn
Napaumpaiporn, Pondpan
Kittiwongwattana, Chokchai
Sakulkoo, Jenjira
Suttangkakul, Anongpat
Vuttipongchaikij, Supachai
Date Issued
July 1, 2022
Type
Article
DOI
10.2144/btn-2022-0013
Abstract
We demonstrate that gDNA can be conveniently and efficiently isolated and purified using standard agarose gel electrophoresis, band excision and gel purification. This method yields a substantial amount at microgram levels of gDNA per gel cleanup with high purity. An RNase A treatment step can be omitted. The quality of gDNA is suitable for next-generation sequencing, resulting in >10 Mb reads and high-quality read data (Phred score >28 up to 100 of 150 base reads). Furthermore, the gDNA can be kept intact in a gel slice for several days. This method has been tested for dictyostelids, bacteria and plants.
Citation
Biotechniques, 73(2), 99-103, 2022
Subjects

agarose gel electroph...

dictyostelium

DNA isolation

gDNA

next-generation seque...

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