| Literature DB >> 1839500 |
N R Isola1, H J Harn, D L Cooper.
Abstract
We describe an expeditious method for the isolation of cDNA clones utilizing PCR-based amplification of target sequences from cDNA libraries. This method is rapid, less labor-intensive and inexpensive when compared with screening libraries with radiolabeled probes. This method can be applied to isolate multiple members of a protein family as well as homologous genes in different species by designing appropriate primers to amplify the most conserved regions. Utilizing this method, a novel reticulocyte CD44 transcript was isolated.Entities:
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Year: 1991 PMID: 1839500
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993