■ 基本信息
別名: | pmir-GLO |
啟動(dòng)子: | PGK |
復制子: | pUC |
終止子: | SV40 poly(A) signal |
質(zhì)粒分類(lèi): | 哺乳細胞，信號通路報告載體 |
質(zhì)粒大小: | 7350bp |
原核抗性: | Amp |
真核抗性: | G418 |
克隆菌株: | DH5a |
培養條件: | 37度 |
表達宿主: | 哺乳細胞 |
誘導方式: | 無(wú)須誘導，瞬時(shí)表達 |
5'測序引物: | PmirGLO-F：GACGAGGTGCCTAAAGGACT |
3'測序引物:
| 根據序列設計引物
|
備注: | 信號報告空載體 |
■ 質(zhì)粒屬性
質(zhì)粒宿主: | 哺乳細胞 |
質(zhì)粒用途: | 信號報告 |
片段類(lèi)型: | miRNA,UTR
|
片段物種: | 空載體
|
原核抗性: | Amp |
真核抗性: | G418 |
熒光標記: | Fluc,Rluc
|
■ 質(zhì)粒簡(jiǎn)介
The pmirGLO Dual-Luciferase miRNA Target Expression Vector(a–d) is designed to quantitatively evaluate microRNA (miRNA) activity by the insertion of miRNA target sites 3′ of the firefly luciferase gene (luc2). These target sites can be introduced by cloning putative miRNA binding sites alone, or the 3′ untranslated region (UTR) of a gene of interest, to study the influence of these sites on transcript stability and activity. Firefly luciferase is the primary reporter gene; reduced firefly luciferase expression indicates the binding of endogenous or introduced miRNAs to the cloned miRNA target sequence. This vector is based on Promega dual-luciferase technology, with firefly luciferase (luc2) used as the primary reporter to monitor mRNA regulation and Renilla luciferase (hRluc-neo) acting as a control reporter for normalization and selection.
■ 質(zhì)粒圖譜
■ 質(zhì)粒序列
質(zhì)粒序列請下載：
ZK515pmirGLO哺乳報告質(zhì)粒.txt
