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1 riable (V)beta-diversity (D)beta-joining(J)beta fingerprint generated by PCR amplification, and determined the primary st
2 h CMO cDNA (1,622 bp) was cloned from spinach using a probe generated by PCR amplification for which the primers were bas
3                                   An initial cDNA clone was generated by PCR amplification using degenerate oligo primers
4                                             env clones were generated by PCR amplification of proviral env sequences, fol
5 tated binding sites for putative transcription factors were generated by PCR amplification and assessed for transcription
6                            Single-stranded RNA targets were generated by PCR amplification of individual BRCA1 exons usin

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