求助,帮忙翻译一篇摘要,汉译英,谢谢! 10

本研究选取转录调节因子Slr0895作为目的基因,从集胞藻Synechocystissp.PCC6803中提取基因组,通过PCR扩增得到目的基因上下游片段作为同源臂构建基... 本研究选取转录调节因子Slr0895作为目的基因,从集胞藻Synechocystis sp. PCC 6803 中提取基因组,通过PCR扩增得到目的基因上下游片段作为同源臂构建基因敲除所需片段,在两个同源片段中间插入氯霉素(chloramphenicol,简称Cm)抗性基因片段,借助琼脂糖电泳来验证融合是否成功。由于集胞藻Synechocystis sp. PCC 6803 有天然的吸收外源DNA的能力,利用这一特性将融合好的突变片段转入集胞藻Synechocystis sp. PCC 6803 细胞中,在含有氯霉素的抗性平板上培养数天直至长出单菌落,再进行菌落PCR来快速鉴定目的基因是否得到成功敲除。将突变株与野生型进行比较,观察其表型。 展开
 我来答
守望者的罗夏Cy
2012-05-25
知道答主
回答量:12
采纳率:0%
帮助的人:6.9万
展开全部
This study selected transcription factor Slr0895as gene, from Synechocystis sp. PCC 6803Synechocystis genome by gene, amplified by PCR downstream fragments as homologous arm knockout constructs required fragment, in two homologous fragment is inserted into the middle of chloramphenicol ( chloramphenicol, Cm) resistance gene fragment, with the help of agarose gel electrophoresis to verify whether successful fusion. As a result of Synechocystis Synechocystis sp. PCC 6803is the natural absorption of exogenous DNA ability, use this property to the fused the mutant fragment into Synechocystis Synechocystis sp. PCC 6803 cells, in containing chloramphenicol resistance plate cultured for several days until a single colony, colony PCR again to rapid identification of target genes is success knockout. The mutant and wild type were compared, to observe its phenotype.
莎旺521
2012-05-31
知道答主
回答量:25
采纳率:0%
帮助的人:13.8万
展开全部
This study selected transcription factor Slr0895 as gene, from Synechocystis sp. PCC 6803 Synechocystis genome by gene, amplified by PCR downstream fragments as homologous arm knockout constructs required fragment, in two homologous fragment is inserted into the middle of chloramphenicol (chloramphenicol, Cm) resistance gene fragment, with the help of agarose gel electrophoresis to verify whether successful fusion.As a result of Synechocystis Synechocystis sp. PCC 6803 is the natural absorption of exogenous DNA ability, use this property to the fused the mutant fragment into Synechocystis Synechocystis sp. PCC 6803 cells, in containing chloramphenicol resistance plate cultured for several days until a single colony, colony PCR again to rapid identification of target genes is success knockout.The mutant and wild type were compared, to observe its phenotype.
已赞过 已踩过<
你对这个回答的评价是?
评论 收起
推荐律师服务: 若未解决您的问题,请您详细描述您的问题,通过百度律临进行免费专业咨询

为你推荐:

下载百度知道APP,抢鲜体验
使用百度知道APP,立即抢鲜体验。你的手机镜头里或许有别人想知道的答案。
扫描二维码下载
×

类别

我们会通过消息、邮箱等方式尽快将举报结果通知您。

说明

0/200

提交
取消

辅 助

模 式