Klonierung von RSV‐cDNS (Respiratiorisches Syncytial Virus) und erste Charakterisierung der Rekombinanten

S. Prösch, W. Seidel, L. Döhner, D. Liebscher
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Abstract

Genomic RNA of the Respiratory syntical virus (RS-virus) was used as a template to synthesize calfthymus DNA-primed cDNAs. These cDNAs were subsequently cloned into the E. coli plasmid pBR 322 at the PstI-site. By hybridization 6 recombinants with virusspecific cDNAs representing 10% of the whole genome could be isolated.
‐Klonierung的感染cDNS (Respiratiorisches Syncytial病毒)和第一个特性Rekombinanten
以呼吸道合胞病毒(rs病毒)基因组RNA为模板,合成胸腺dna引物cdna。这些cdna随后在psti位点被克隆到大肠杆菌质粒pBR 322中。通过与病毒特异性cdna的杂交,可以分离出6个重组体,占整个基因组的10%。
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