Cloning BRD4 long isoform into overexpression vectors for stable overexpression of BRD4-L in mammalian cells.
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ABSTRACT: Molecular cloning of BRD4-L is a challenging technique, because the DNA insert is formed by a long, GC-rich sequence, which folds into secondary structures. The present protocol defines a specific strategy to amplify BRD4-L, followed by the successful cloning of the gene into an overexpression vector. Since there are no existing protocols nor commercially available plasmids, this work provides a useful tool for studies involving molecular cloning of BRD4-L and could potentially be applied to other challenging genes.
SUBMITTER: Drumond-Bock AL
PROVIDER: S-EPMC9617197 | biostudies-literature | 2022 Dec
REPOSITORIES: biostudies-literature
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