pcDNA6.2/V5-PL-DEST Gateway載體
- 價(jià) 格:¥4920
- 貨 號(hào):3735070
- 產(chǎn) 地:北京
- BioVector NTCC典型培養(yǎng)物保藏中心
- 聯(lián)系人:Dr.Xu, Biovector NTCC Inc.
電話(huà):400-800-2947 工作微信:1843439339 (QQ同號(hào))
手機(jī):18901268599
地址:北京
- 已注冊(cè)
載體名稱(chēng):pcDNA6.2/V5-PL-DEST Gateway載體
基本信息
| 出品公司: | Invitrigen |
|---|---|
| 載體名稱(chēng): | pcDNA6.2/V5-PL-DEST |
| 質(zhì)粒類(lèi)型: | Gateway載體;哺乳動(dòng)物表達(dá)載體;cDNA克隆與表達(dá) |
| 高拷貝/低拷貝: | 高拷貝 |
| 啟動(dòng)子: | 無(wú)啟動(dòng)子 |
| 克隆方法: | Gateway |
| 載體大小: | 6693 bp |
| 5 測(cè)序引物及序列: | T7 Forward 5′-TAATACGACTCACTATAGGG-3′ |
| 3 測(cè)序引物及序列: | V5 Reverse 5′-ACCGAGGAGAGGGTTAGGGAT-3′ |
| 載體標(biāo)簽: | V5 Epitope Tag(C-端) |
| 載體抗性: | 氨芐青霉素、氯霉素(僅空載體) |
| 篩選標(biāo)記: | Blasticidin |
| 克隆菌株: | DB3.1 |
| 宿主細(xì)胞(系): | 常規(guī)細(xì)胞系,如293、Hela等 |
| 備注: | pcDNA6.2/V5-PL-DEST載體沒(méi)有啟動(dòng)子,可用于啟動(dòng)子功能研究和多基因表達(dá)。 |
| 產(chǎn)品目錄號(hào): | 12537-162 |
| 穩(wěn)定性: | 瞬表達(dá) 或 穩(wěn)表達(dá) |
| 組成型: | 組成型 |
| 病毒/非病毒: | 非病毒 |
質(zhì)粒圖譜

載體簡(jiǎn)介
載體特征 pcDNA6.2/V5-pL-DEST載體含有以下元件: • Two recombination sites, attR1 and attR2 for recombinational cloning of up to 4 entry clones when using MultiSite Gateway Pro kits • The ccdB gene located between the two attR sites for negative selection • Chloramphenicol resistance gene located between the two attR sites for counterscreening • The V5 epitope tag for easy detection using Anti-V5 antibodies • The Herpes Simplex Virus thymidine kinase polyadenylation signal for proper termination and processing of the recombinant transcript • f1 intergenic region for production of single-strand DNA in F plasmid-containing E. coli • SV40 early promoter and origin for expression of the Blasticidin resistance gene and stable propagation of the plasmid in mammalian hosts expressing the SV40 large T antigen • Blasticidin resistance gene for efficient selection of stable cell lines • The pUC origin for high copy replication and maintenance of the plasmid in E. coli • The ampicillin (bla) resistance gene for selection in E. coli Gateway技術(shù) The Gateway Technology is a universal cloning method that takes advantage of the site-specific recombination properties of bacteriophage lambda (Landy, 1989) to provide a rapid and highly efficient way to move your gene of interest into multiple vector systems. To express your gene of interest using Gateway Technology, simply: 1. Generate entry clones containing your promoter and gene(s) of interest. 2. Generate an expression clone by performing an LR recombination reaction between the entry clone(s) and pcDNA6.2/V5-pL-DEST). 3. Transfect your expression clone into cells of your choice to transiently or stably express your gene of interest. To fit all of your expression needs, Invitrogen offers state-of-the-art Gateway destination vectors for expression in E. coli, insect, yeast, or mammalian cells, as well as for production of native protein or N- or C-terminal fusion proteins. All Gateway destination vectors have attR sites for recombination with any attL-flanked fragment, regardless of whether it is an entry clone or an Ultimate ORF Clone. The following table lists a variety of available destination vectors. Additional materials required, available separately: Gateway entry clone, appropriate Gateway LR Clonase enzyme mix, and reaction buffer. 所需材料 在著手開(kāi)始實(shí)驗(yàn)前你需要準(zhǔn)備一下材料: Gateway entry clone, appropriate Gateway LR Clonase enzyme mix, and reaction buffer. • Purified plasmid DNA of your entry clone(s) (10 fmoles each) • pcDNA6.2/V5-pL-DEST (20 fmoles) • LR Clonase II Plus enzyme mix (keep at –20°C until immediately before use) • 1X TE Buffer, pH 8.0 (10 mM Tris-HCl, pH 8.0, 1 mM EDTA) • 2 μg/μL Proteinase K solution (supplied with the enzyme mix; thaw and keep on ice until use) • Appropriate competent E. coli host and growth media for expression • S.O.C. Medium • LB agar plates containing 100 μg/mL ampicillin 進(jìn)行LR重組反應(yīng) 值得注意的事項(xiàng): If you use E. coli cells with a transformation efficiency of ≥1 × 108 cfu/μg, a typical LR reaction should give >5,000 colonies if the entire reaction is transformed and plated. For multiple fragment reactions, typical numbers of colonies (per 10 μL LR reaction) are: • 2-fragment recombination reaction: 2,000–15,000 • 3-fragment recombination reaction: 1,000–5,000 • 4-fragment recombination reaction: 50–500
載體序列
AGTGCGCGAGCAAAATTTAAGCTACAACAAGGCAAGGCTTGACCGACAATTCTCTGGCTAACTAGAGAAC CCACTGCTTACTGGCTTATCGAAATTAATACGACTCACTATAGGGAGACCCAAGCTGGCTAGTTAAGCTA TCAACAAGTTTGTACAAAAAAGCTGAACGAGAAACGTAAAATGATATAAATATCAATATATTAAATTAGA TTTTGCATAAAAAACAGACTACATAATACTGTAAAACACAACATATCCAGTCACTATGAATCAACTACTT AGATGGTATTAGTGACCTGTAGTCGACCGACAGCCTTCCAAATGTTCTTCGGGTGATGCTGCCAACTTAG TCGACCGACAGCCTTCCAAATGTTCTTCTCAAACGGAATCGTCGTATCCAGCCTACTCGCTATTGTCCTC AATGCCGTATTAAATCATAAAAAGAAATAAGAAAAAGAGGTGCGAGCCTCTTTTTTGTGTGACAAAATAA AAACATCTACCTATTCATATACGCTAGTGTCATAGTCCTGAAAATCATCTGCATCAAGAACAATTTCACA ACTCTTATACTTTTCTCTTACAAGTCGTTCGGCTTCATCTGGATTTTCAGCCTCTATACTTACTAAACGT GATAAAGTTTCTGTAATTTCTACTGTATCGACCTGCAGACTGGCTGTGTATAAGGGAGCCTGACATTTAT ATTCCCCAGAACATCAGGTTAATGGCGTTTTTGATGTCATTTTCGCGGTGGCTGAGATCAGCCACTTCTT CCCCGATAACGGAGACCGGCACACTGGCCATATCGGTGGTCATCATGCGCCAGCTTTCATCCCCGATATG CACCACCGGGTAAAGTTCACGGGAGACTTTATCTGACAGCAGACGTGCACTGGCCAGGGGGATCACCATC CGTCGCCCGGGCGTGTCAATAATATCACTCTGTACATCCACAAACAGACGATAACGGCTCTCTCTTTTAT AGGTGTAAACCTTAAACTGCATTTCACCAGCCCCTGTTCTCGTCAGCAAAAGAGCCGTTCATTTCAATAA ACCGGGCGACCTCAGCCATCCCTTCCTGATTTTCCGCTTTCCAGCGTTCGGCACGCAGACGACGGGCTTC ATTCTGCATGGTTGTGCTTACCAGACCGGAGATATTGACATCATATATGCCTTGAGCAACTGATAGCTGT CGCTGTCAACTGTCACTGTAATACGCTGCTTCATAGCATACCTCTTTTTGACATACTTCGGGTATACATA TCAGTATATATTCTTATACCGCAAAAATCAGCGCGCAAATACGCATACTGTTATCTGGCTTTTAGTAAGC CGGATCCACGCGGCGTTTACGCCCCCCCTGCCACTCATCGCAGTACTGTTGTAATTCATTAAGCATTCTG CCGACATGGAAGCCATCACAAACGGCATGATGAACCTGAATCGCCAGCGGCATCAGCACCTTGTCGCCTT GCGTATAATATTTGCCCATGGTGAAAACGGGGGCGAAGAAGTTGTCCATATTGGCCACGTTTAAATCAAA ACTGGTGAAACTCACCCAGGGATTGGCTGAGACGAAAAACATATTCTCAATAAACCCTTTAGGGAAATAG GCCAGGTTTTCACCGTAACACGCCACATCTTGCGAATATATGTGTAGAAACTGCCGGAAATCGTCGTGGT ATTCACTCCAGAGCGATGAAAACGTTTCAGTTTGCTCATGGAAAACGGTGTAACAAGGGTGAACACTATC CCATATCACCAGCTCACCGTCTTTCATTGCCATACGGAATTCCGGATGAGCATTCATCAGGCGGGCAAGA ATGTGAATAAAGGCCGGATAAAACTTGTGCTTATTTTTCTTTACGGTCTTTAAAAAGGCCGTAATATCCA GCTGAACGGTCTGGTTATAGGTACATTGAGCAACTGACTGAAATGCCTCAAAATGTTCTTTACGATGCCA TTGGGATATATCAACGGTGGTATATCCAGTGATTTTTTTCTCCATTTTAGCTTCCTTAGCTCCTGAAAAT CTCGATAACTCAAAAAATACGCCCGGTAGTGATCTTATTTCATTATGGTGAAAGTTGGAACCTCTTACGT GCCGATCAACGTCTCATTTTCGCCAAAAGTTGGCCCAGGGCTTCCCGGTATCAACAGGGACACCAGGATT TATTTATTCTGCGAAGTGATCTTCCGTCACAGGTATTTATTCGGCGCAAAGTGCGTCGGGTGATGCTGCC AACTTAGTCGACTACAGGTCACTAATACCATCTAAGTAGTTGATTCATAGTGACTGGATATGTTGTGTTT TACAGTATTATGTAGTCTGTTTTTTATGCAAAATCTAATTTAATATATTGATATTTATATCATTTTACGT TTCTCGTTCAGCTTTCTTGTACAAAGTGGTTGATCTAGAGGGCCCGCGGTTCGAAGGTAAGCCTATCCCT AACCCTCTCCTCGGTCTCGATTCTACGCGTACCGGTTAGTAATGAGTTTAAACGGGGGAGGCTAACTGAA ACACGGAAGGAGACAATACCGGAAGGAACCCGCGCTATGACGGCAATAAAAAGACAGAATAAAACGCACG GGTGTTGGGTCGTTTGTTCATAAACGCGGGGTTCGGTCCCAGGGCTGGCACTCTGTCGATACCCCACCGA GACCCCATTGGGGCCAATACGCCCGCGTTTCTTCCTTTTCCCCACCCCACCCCCCAAGTTCGGGTGAAGG CCCAGGGCTCGCAGCCAACGTCGGGGCGGCAGGCCCTGCCATAGCAGATCTGCGCAGCTGGGGCTCTAGG GGGTATCCCCACGCGCCCTGTAGCGGCGCATTAAGCGCGGCGGGTGTGGTGGTTACGCGCAGCGTGACCG CTACACTTGCCAGCGCCCTAGCGCCCGCTCCTTTCGCTTTCTTCCCTTCCTTTCTCGCCACGTTCGCCGG CTTTCCCCGTCAAGCTCTAAATCGGGGGCTCCCTTTAGGGTTCCGATTTAGTGCTTTACGGCACCTCGAC CCCAAAAAACTTGATTAGGGTGATGGTTCACGTAGTGGGCCATCGCCCTGATAGACGGTTTTTCGCCCTT TGACGTTGGAGTCCACGTTCTTTAATAGTGGACTCTTGTTCCAAACTGGAACAACACTCAACCCTATCTC GGTCTATTCTTTTGATTTATAAGGGATTTTGCCGATTTCGGCCTATTGGTTAAAAAATGAGCTGATTTAA CAAAAATTTAACGCGAATTAATTCTGTGGAATGTGTGTCAGTTAGGGTGTGGAAAGTCCCCAGGCTCCCC AGCAGGCAGAAGTATGCAAAGCATGCATCTCAATTAGTCAGCAACCAGGTGTGGAAAGTCCCCAGGCTCC CCAGCAGGCAGAAGTATGCAAAGCATGCATCTCAATTAGTCAGCAACCATAGTCCCGCCCCTAACTCCGC CCATCCCGCCCCTAACTCCGCCCAGTTCCGCCCATTCTCCGCCCCATGGCTGACTAATTTTTTTTATTTA TGCAGAGGCCGAGGCCGCCTCTGCCTCTGAGCTATTCCAGAAGTAGTGAGGAGGCTTTTTTGGAGGCCTA GGCTTTTGCAAAAAGCTCCCGGGAGCTTGTATATCCATTTTCGGATCTGATCAGCACGTGTTGACAATTA ATCATCGGCATAGTATATCGGCATAGTATAATACGACAAGGTGAGGAACTAAACCATGGCCAAGCCTTTG TCTCAAGAAGAATCCACCCTCATTGAAAGAGCAACGGCTACAATCAACAGCATCCCCATCTCTGAAGACT ACAGCGTCGCCAGCGCAGCTCTCTCTAGCGACGGCCGCATCTTCACTGGTGTCAATGTATATCATTTTAC TGGGGGACCTTGTGCAGAACTCGTGGTGCTGGGCACTGCTGCTGCTGCGGCAGCTGGCAACCTGACTTGT ATCGTCGCGATCGGAAATGAGAACAGGGGCATCTTGAGCCCCTGCGGACGGTGCCGACAGGTGCTTCTCG ATCTGCATCCTGGGATCAAAGCCATAGTGAAGGACAGTGATGGACAGCCGACGGCAGTTGGGATTCGTGA ATTGCTGCCCTCTGGTTATGTGTGGGAGGGCTAAGCACTTCGTGGCCGAGGAGCAGGACTGACACGTGCT ACGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGGTTGGGCTTCGGAATCGTTTTCCGGGACGCCGGC TGGATGATCCTCCAGCGCGGGGATCTCATGCTGGAGTTCTTCGCCCACCCCAACTTGTTTATTGCAGCTT ATAATGGTTACAAATAAAGCAATAGCATCACAAATTTCACAAATAAAGCATTTTTTTCACTGCATTCTAG TTGTGGTTTGTCCAAACTCATCAATGTATCTTATCATGTCTGTATACCGTCGACCTCTAGCTAGAGCTTG GCGTAATCATGGTCATAGCTGTTTCCTGTGTGAAATTGTTATCCGCTCACAATTCCACACAACATACGAG CCGGAAGCATAAAGTGTAAAGCCTGGGGTGCCTAATGAGTGAGCTAACTCACATTAATTGCGTTGCGCTC ACTGCCCGCTTTCCAGTCGGGAAACCTGTCGTGCCAGCTGCATTAATGAATCGGCCAACGCGCGGGGAGA GGCGGTTTGCGTATTGGGCGCTCTTCCGCTTCCTCGCTCACTGACTCGCTGCGCTCGGTCGTTCGGCTGC GGCGAGCGGTATCAGCTCACTCAAAGGCGGTAATACGGTTATCCACAGAATCAGGGGATAACGCAGGAAA GAACATGTGAGCAAAAGGCCAGCAAAAGGCCAGGAACCGTAAAAAGGCCGCGTTGCTGGCGTTTTTCCAT AGGCTCCGCCCCCCTGACGAGCATCACAAAAATCGACGCTCAAGTCAGAGGTGGCGAAACCCGACAGGAC TATAAAGATACCAGGCGTTTCCCCCTGGAAGCTCCCTCGTGCGCTCTCCTGTTCCGACCCTGCCGCTTAC CGGATACCTGTCCGCCTTTCTCCCTTCGGGAAGCGTGGCGCTTTCTCATAGCTCACGCTGTAGGTATCTC AGTTCGGTGTAGGTCGTTCGCTCCAAGCTGGGCTGTGTGCACGAACCCCCCGTTCAGCCCGACCGCTGCG CCTTATCCGGTAACTATCGTCTTGAGTCCAACCCGGTAAGACACGACTTATCGCCACTGGCAGCAGCCAC TGGTAACAGGATTAGCAGAGCGAGGTATGTAGGCGGTGCTACAGAGTTCTTGAAGTGGTGGCCTAACTAC GGCTACACTAGAAGAACAGTATTTGGTATCTGCGCTCTGCTGAAGCCAGTTACCTTCGGAAAAAGAGTTG GTAGCTCTTGATCCGGCAAACAAACCACCGCTGGTAGCGGTGGTTTTTTTGTTTGCAAGCAGCAGATTAC GCGCAGAAAAAAAGGATCTCAAGAAGATCCTTTGATCTTTTCTACGGGGTCTGACGCTCAGTGGAACGAA AACTCACGTTAAGGGATTTTGGTCATGAGATTATCAAAAAGGATCTTCACCTAGATCCTTTTAAATTAAA AATGAAGTTTTAAATCAATCTAAAGTATATATGAGTAAACTTGGTCTGACAGTTACCAATGCTTAATCAG TGAGGCACCTATCTCAGCGATCTGTCTATTTCGTTCATCCATAGTTGCCTGACTCCCCGTCGTGTAGATA ACTACGATACGGGAGGGCTTACCATCTGGCCCCAGTGCTGCAATGATACCGCGAGACCCACGCTCACCGG CTCCAGATTTATCAGCAATAAACCAGCCAGCCGGAAGGGCCGAGCGCAGAAGTGGTCCTGCAACTTTATC CGCCTCCATCCAGTCTATTAATTGTTGCCGGGAAGCTAGAGTAAGTAGTTCGCCAGTTAATAGTTTGCGC AACGTTGTTGCCATTGCTACAGGCATCGTGGTGTCACGCTCGTCGTTTGGTATGGCTTCATTCAGCTCCG GTTCCCAACGATCAAGGCGAGTTACATGATCCCCCATGTTGTGCAAAAAAGCGGTTAGCTCCTTCGGTCC TCCGATCGTTGTCAGAAGTAAGTTGGCCGCAGTGTTATCACTCATGGTTATGGCAGCACTGCATAATTCT CTTACTGTCATGCCATCCGTAAGATGCTTTTCTGTGACTGGTGAGTACTCAACCAAGTCATTCTGAGAAT AGTGTATGCGGCGACCGAGTTGCTCTTGCCCGGCGTCAATACGGGATAATACCGCGCCACATAGCAGAAC TTTAAAAGTGCTCATCATTGGAAAACGTTCTTCGGGGCGAAAACTCTCAAGGATCTTACCGCTGTTGAGA TCCAGTTCGATGTAACCCACTCGTGCACCCAACTGATCTTCAGCATCTTTTACTTTCACCAGCGTTTCTG GGTGAGCAAAAACAGGAAGGCAAAATGCCGCAAAAAAGGGAATAAGGGCGACACGGAAATGTTGAATACT CATACTCTTCCTTTTTCAATATTATTGAAGCATTTATCAGGGTTATTGTCTCATGAGCGGATACATATTT GAATGTATTTAGAAAAATAAACAAATAGGGGTTCCGCGCACATTTCCCCGAAAAGTGCCACCTGACGTCG ACGGATCGGGAGATCTCCCGATCCCCTATGGTGCACTCTCAGTACAATCTGCTCTGATGCCGCATAGTTA AGCCAGTATCTGCTCCCTGCTTGTGTGTTGGAGGTCGCTGAGT
BioVector NTCC Inc.產(chǎn)品分類(lèi)目錄簡(jiǎn)介
Biovector質(zhì)粒載體菌株細(xì)胞株基因庫(kù)-NTCC典型培養(yǎng)物保藏中心,可提供數(shù)萬(wàn)種質(zhì)粒載體、菌株、基因和細(xì)胞株,并可提供實(shí)驗(yàn)技術(shù)外包服務(wù),如基因克隆、質(zhì)粒構(gòu)建、蛋白原核、真核表達(dá)及純化、病毒包裝、基因沉默RNAi等服務(wù)。,Biovector NTCC Inc.可為您提供便捷一站式的產(chǎn)品進(jìn)口服務(wù),到貨快捷,步驟簡(jiǎn)便。
BioVector質(zhì)粒載體菌株細(xì)胞基因保藏中心
NTCC典型培養(yǎng)物保藏中心
電話(huà):010-53513060,
技術(shù)支持及訂購(gòu)服務(wù):18901268599
電郵[email protected]
訂購(gòu)QQ:1843439339
Biovector NTCC中心主頁(yè)www.nedfriskphoto.com
資源分類(lèi)列表網(wǎng)址http://Biovector.1688.com
博客地址http://biovector.blog.163.com
通過(guò)Google搜索"Biovector+您所需資源名稱(chēng)",您一定能找到所需的資源和技術(shù)服務(wù)。
資源涵蓋克隆載體、真核表達(dá)載體、原核表達(dá)載體、病毒載體、信號(hào)通路報(bào)告載體、亞細(xì)胞定位載體、熒光蛋白載體、昆蟲(chóng)細(xì)胞表達(dá)載體、啟動(dòng)子載體、誘導(dǎo)調(diào)控載體等十多種類(lèi)型上萬(wàn)個(gè)品種。
我們擁有目前最大的cDNA克隆庫(kù)、覆蓋30,000個(gè)人全長(zhǎng)基因的TrueClone cDNA克隆和超過(guò)25,000個(gè)TrueORF cDNA克隆。利用TrueORF cDNA克隆,我們開(kāi)發(fā)了大量的全長(zhǎng)人重組蛋白產(chǎn)品(哺乳動(dòng)物細(xì)胞表達(dá)),可以進(jìn)行蛋白功能的研究。另外,Biovector,Inc提供獨(dú)特的基因表達(dá)產(chǎn)品,如TissueScan cancer qPCR array用于生物標(biāo)記物的發(fā)現(xiàn)及鑒定。
33,000 種人TrueClones 全長(zhǎng)人cDNA克隆(無(wú)標(biāo)簽)
5,000種 小鼠 TrueClones 全長(zhǎng)小鼠cDNA克?。o(wú)標(biāo)簽)
25,000 種人 TrueORF 人ORF cDNA克隆(帶標(biāo)簽)
12,000種 小鼠 TrueORF 小鼠ORF cDNA克?。◣?biāo)簽)
5,000種 人重組蛋白 全長(zhǎng)的人重組蛋白(HEK293T細(xì)胞表達(dá))
5,000 種 一抗 經(jīng)鑒定的特異性識(shí)別人源蛋白的一抗產(chǎn)品
25,000 種人 HuSH-29 shRNA 預(yù)設(shè)計(jì)的shRNA 表達(dá)載體(人基因),用于基因沉默
20,000 種小鼠 HuSH-29 shRNA 預(yù)設(shè)計(jì)的shRNA 表達(dá)載體(小鼠基因),用于基因沉默
您正在向 biovector.net 發(fā)送關(guān)于產(chǎn)品 pcDNA6.2/V5-PL-DEST Gateway載體 的詢(xún)問(wèn)
- 公告/新聞







