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Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene.

To identify CA repeats in genomic sequences which had been previously subcloned into plasmids, we performed PCR using a (CA)n primer and a flanking vector primer on the genomic inserts. By incorporation of a restriction enzyme site into the (CA)n primer, we have been able to subclone the genomic DNA...

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Dettagli Bibliografici
Autori principali: Feener, C A, Boyce, F M, Kunkel, L M
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1991
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682967/
https://ncbi.nlm.nih.gov/pubmed/1998344
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