摘要
用根据GRF设计的引物,以猪的下丘脑总RNA和mRNA为模板、进行RT—PCR扩增.将扩增产物纯化并克隆到T载体(pGEM3—Zf),自动测序仪测定其序列.发现所克隆的基因并非GRF基因.应用BLAST软件对其在INTERNET作了分析,未能确定为何种基因.
We designed a experiment to obtain porcine GRF cDNA. Total RNA and mRNA were extracted from porcine hypotheiemus. Primers were designed according to publised porcine GRF cDNA sequence. RT-PCR was carried out to the standard method. PCRproduct was cloned to T-vector. Positive clone was selected and sequenced. The result showed that the cloned cDNA was not GRF gene. We anylyzed the sequence in Internet by Blast, finding no similar.
出处
《生物技术》
CAS
CSCD
1998年第1期7-9,共3页
Biotechnology