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用于果蝇P因子介导转化和组织培养转染的载体。

Vectors for Drosophila P-element-mediated transformation and tissue culture transfection.

作者信息

Thummel C S, Boulet A M, Lipshitz H D

机构信息

Howard Hughes Medical Institute, Department of Human Genetics, University of Utah Medical Center, Salt Lake City 84132.

出版信息

Gene. 1988 Dec 30;74(2):445-56. doi: 10.1016/0378-1119(88)90177-1.

Abstract

We describe nine P-element vectors that can be used to study gene regulation and function in Drosophila. These vectors were designed for use in germline transformation and cell culture transfection assays. One set consists of five P elements that can be used to study transcriptional regulatory sequences. These vectors contain several unique restriction sites for insertion of a foreign promoter upstream from either a cat or lacZ reporter gene. Two of the beta-galactosidase-coding vectors also require the insertion of a start codon for translation of the reporter enzyme and thus can be used to study translational regulatory sequences. The second set of P elements consists of four vectors that contain the Drosophila cytoplasmic actin 5C promoter and polyadenylation signals. Upon insertion of a foreign DNA segment, these vectors direct constitutive expression of the encoded RNA and protein.

摘要

我们描述了九种可用于研究果蝇基因调控和功能的P元素载体。这些载体设计用于生殖系转化和细胞培养转染实验。一组由五个可用于研究转录调控序列的P元素组成。这些载体含有几个独特的限制性酶切位点,用于在cat或lacZ报告基因上游插入外源启动子。两个β-半乳糖苷酶编码载体还需要插入起始密码子以翻译报告酶,因此可用于研究翻译调控序列。第二组P元素由四个载体组成,这些载体含有果蝇细胞质肌动蛋白5C启动子和聚腺苷酸化信号。插入外源DNA片段后,这些载体指导编码的RNA和蛋白质的组成型表达。

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