pRI201-AN載體基本信息
載體名稱: | pRI201-AN |
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質粒類型: | 雙子葉植物載體;農桿菌雙元表達載體;雙表達載體 |
高拷貝/低拷貝: | 高拷貝 |
克隆方法: | 限制性內切酶,多克隆位點 |
啟動子: | 35S |
載體大小: | 10432 bp |
5' 測序引物及序列: | 35S promoter 5’CTATCCTTCGCAAGACCCTTC 3’ |
3' 測序引物及序列: | ATTCAGAATTGTCGANNNNNNNNNNNNNNNNN |
載體標簽: | 無 |
載體抗性: | Kanamycin.html' target='_blank'>卡那霉素 |
篩選標記: | 新霉素 |
克隆菌株: | HB101 |
宿主細胞(系): | 植物細胞、農桿菌 |
備注: | pRI201-AN載體是一種在雙子葉植物細胞中表達外源基因的載;可同時表達2個外源基因;利用發(fā)根土壤桿菌介導。 |
產品目錄號: | 3264 |
穩(wěn)定性: | 穩(wěn)表達 |
組成型/誘導型: | 組成型 |
病毒/非病毒: | 非病毒 |
pRI201-AN載體簡介 The Ri Plasmid pRI201 is designed for the transformation and expression of target genes from plant cells. This series of binary vectors for plant transformation retains the backbone of the pRI101 vectors, including an alcohol dehydrogenase (ADH) gene-derived 5' untranslated region (5'-UTR) downstream of the cauliflower mosaic virus (CaMV promoter)-derived 35S promoter. Additionally, these vectors have a heat shock protein (HSP) gene-derived terminator in place of the nopaline synthase (NOS) gene-derived terminator, allowing higher target gene expression compared with the pRI101 vector series. Multigene transformation with a single vector can be achieved by integrating an expression cassette containing another gene (promoter + enhancer + gene of interest + terminator) into the vector's second multiple cloning site (MCS2) located downstream of the HSP terminator. The Ri Plasmid pRI201 binary vector series offers two types of vectors: pRI 201-AN DNA and pRI 201-ON DNA. pRI 201-AN DNA contains an Arabidopsis ADH-derived 5' UTR (AtADH 5'-UTR) and is suitable for dicotyledonous plant transformation. pRI 201-ON DNA contains a rice ADH-derived 5' UTR (OsADH 5'-UTR) and is suitable for monocotyledonous plant transformation. The pRI 201-AN DNA and pRI 201-ON DNA binary vectors for plant transformation have a mutant-type replication origin (Ri ori) from the Rhizobium rhizogenes Ri plasmid. These vectors also contain a replication origin (ColE1 ori) derived from the pUC plasmid; the ColE1 ori allows high copy number replication in E. coli. The vectors' multiple cloning site, located near the right border (RB) of T-DNA, allows stable target gene integration into the plant chromosome. pRI201-AN載體特征: Use pRI 201-AN DNA to transform dicotyledonous plant species Use pRI 201-ON DNA to transform monocotyledonous plant species Integrate multiple transgenes using a single vector High copy number (ColE1 ori) replication in E. coli pRI201-AN載體應用: Integration of multiple transgenes Dicotyledonous plant transformation Monocotyledonous plant transformation 參考文獻: 1. Sugio, T. et al. (2008) J. Biosci. Bioeng. 105(3):300-302. 2. Nagaya, S. et al. (2010) Plant & Cell Physiol. 51(2):328-332. 3. Nishiguchi, R. et al. (1987) Mol. Gen. Genet. 206:1-8. 4. Satoh, J. et al. (2004) J. Biosci. and Bioeng. 98(1):1-8. 5. Sugio, T. et al. (2010) J. Biosci. Bioeng. 109(2):170-173.