产品封面图

pCMV-DsRed-Express2载体

收藏
  • ¥2000
  • ZYbscience
  • 中国/美国
  • ZY632539
  • 2026年03月28日
    avatar
  • 企业认证

    点击 QQ 联系

  • 万千商家帮你免费找货

    0 人在求购买到急需产品
    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      -20℃低温保存

    • 保质期

      三年

    • 英文名

      pCMV-DsRed-Express2

    • 库存

      20

    • 供应商

      泽叶生物

    载体基本信息

    出品公司: ZYbscience
    载体名称: pCMV-DsRed-Express2
    质粒类型: 慢病毒载体;荧光报告载体
    高拷贝/低拷贝: 高拷贝
    克隆方法: 限制性内切酶,多克隆位点
    启动子: CMV
    载体大小: 4638 bp
    5' 测序引物及序列: --
    3' 测序引物及序列: --
    载体标签: --
    载体抗性: 卡那霉素
    筛选标记: 新霉素(Neomycin
    克隆菌株: DH5α, HB101
    宿主细胞(系): 常规细胞系(293、CV-1、CHO等)
    备注: pCMV-DsRed-Express2组成型表达DsRed-Express2;
    在DsRed-Express2的上下游留有酶切位点,便于转移到其它载体上去;
    DsRed-Express2是DsRed的突变体,与DsRed相比,DsRed-Express2细胞毒性低,尤其适用于原代细胞和干细胞的荧光标记。
    产品目录号: ZY632539
    稳定性: 稳表达 或 瞬表达
    组成型/诱导型: 组成型
    病毒/非病毒: 非病毒

    载体质粒图谱和多克隆位点信息

    pCMV-DsRed-Express2载体图谱



    pCMV-DsRed-Express2 载体特征

    载体简介

    pCMV-DsRed-Express2载体描述
    
    pCMV DsRed-Express2 is a mammalian expression vector designed to be used for whole cell labeling or as a marker of cotransfection. In mammalian cells, the vector constitutively expresses DsRed-Express2, a variant of the Discosoma sp. red fluorescent protein, DsRed (1). DsRed-Express2 retains the fast maturation and high photostability characteristic of its predecessor, DsRed-Express (2), and has been engineered (through additional amino acid substitutions) for increased solubility (3). Although it most likely forms the same tetrameric structure as wild-type DsRed, DsRed-Express2 displays a greatly reduced tendency to aggregate, resulting in reduced cyto- and phototoxicity, and making DsRed-Express2 much better suited for in vivo applications involving sensitive cells, such as primary or stem cells. In fact, DsRed-Express2 has been shown to be the best red fluorescent protein for whole cell labeling applications (3). DsRed-Express2 also exhibits extremely low residual green fluorescence, which allows cells expressing the protein to be effectively separated from other fluorescently labeled cell populations by flow cytometry. The DsRed-Express2 gene is positioned just downstream of the constitutively active human cytomegalovirus immediate early promoter (PCMV IE). As a result, mammalian cells transfected with this vector will constitutively express the red fluorescent protein. A Kozak consensus sequence (4) has been placed immediately upstream of the DsRed-Express2 coding sequence to enhance translational efficiency in eukaryotic cells. SV40 polyadenylation signals downstream of the DsRed-Express2 gene direct proper processing of the 3' end of the DsRed-Express2 mRNA. The vector backbone contains an SV40 origin for replication in mammalian cells expressing the SV40 large T antigen, a pUC origin of replication for propagation in E. coli, and an f1 origin for single-stranded DNA production. A neomycin resistance cassette (Neor) allows stably transfected eukaryotic cells to be selected using G418 (5). This cassette consists of the SV40 early promoter, a Tn5 kanamycin/neomycin resistance gene, and herpes simplex virus thymidine kinase (HSV TK) polyadenylation signals. A bacterial promoter upstream of the cassette expresses kanamycin resistance in E. coli.
    
    pCMV DsRed-Express2 can be used for whole cell labeling or as a cotransfection marker. The vector can be transfected into mammalian cells using any standard transfection method. Cells expressing DsRed-Express2 (excitation and emission maxima: 554 nm and 591 nm, respectively) can be detected by fluorescence microscopy or flow cytometry 8-12 hours after transfection. If required, stable transfectants can be selected using G418. After cotransfection with pCMV DsRed-Express2 and an expression construct of interest, cells can also be sorted by flow cytometry to enrich for transfected cells.
    
    Propagation in E. coli
     Recommended host strain: DH5α, HB101, and other general purpose strains. Single-stranded DNA production
    requires a host containing an F plasmid such as JM109 or XL1-Blue.
     Selectable marker: plasmid confers resistance to kanamycin (50 μg/ml) in E. coli hosts.
     E. coli replication origin: pUC
     Copy number: high
     Plasmid incompatibility group: pMB1/ColE1
    
    Excitation and emission maxima of DsRed-Express2
     Excitation maximum = 554 nm
     Emission maximum = 591 nm
    
    References
    1. Matz, M. V. et al. (1999) Nat. Biotechnol. 17(10):969-973.
    2. Bevis, B. J. & Glick, B. S. (2002) Nat. Biotechnol. 20(1):83–87. Erratum in Nat. Biotechnol. (2002) 20(11):1159
    3. Strack, R. L. et al. (2008) Nat. Methods 5(11):955–957.
    4. Kozak, M. (1987) Nucleic Acids Res. 15(20): 8125-8148
    5. Gorman, C. (1985) In DNA Cloning: A Practical Approach, Vol. II. Ed. D. M. Glover. (IRL Press, Oxford, U.K.), pp. 143–190.
    
    

    载体序列

    LOCUS       pCMV DsRed-Express2   4638 bp    DNA   circular             8-NOV-2009
    COMMENT     Created by Clontech Laboratories Inc. http://www.clontech.com
    COMMENT     Cat. No. 632539
    FEATURES             Location/Qualifiers
         promoter        1..589
                         /label=CMV\IE\Promoter
                         /note="Human cytomegalovirus (CMV) immediate early promoter"
         CDS             2534..3328
                         /label=Kan(R)/Neo(R)
         rep_origin      3913..4556
                         /label=pUC\ori
         CDS             628..1302
                         /label=DsRed-Express2
    BASE COUNT     1102 a      1252 c      1229 g      1055 t 
    ORIGIN
            1 tagttattaa tagtaatcaa ttacggggtc attagttcat agcccatata tggagttccg 
           61 cgttacataa cttacggtaa atggcccgcc tggctgaccg cccaacgacc cccgcccatt 
          121 gacgtcaata atgacgtatg ttcccatagt aacgccaata gggactttcc attgacgtca 
          181 atgggtggag tatttacggt aaactgccca cttggcagta catcaagtgt atcatatgcc 
          241 aagtacgccc cctattgacg tcaatgacgg taaatggccc gcctggcatt atgcccagta 
          301 catgacctta tgggactttc ctacttggca gtacatctac gtattagtca tcgctattac 
          361 catggtgatg cggttttggc agtacatcaa tgggcgtgga tagcggtttg actcacgggg 
          421 atttccaagt ctccacccca ttgacgtcaa tgggagtttg ttttggcacc aaaatcaacg 
          481 ggactttcca aaatgtcgta acaactccgc cccattgacg caaatgggcg gtaggcgtgt 
          541 acggtgggag gtctatataa gcagagctgg tttagtgaac cgtcagatcc gctagcgcta 
          601 ccggactcag atccaccggt cgccaccatg gatagcactg agaacgtcat caagcccttc 
          661 atgcgcttca aggtgcacat ggagggctcc gtgaacggcc acgagttcga gatcgagggc 
          721 gagggcgagg gcaagcccta cgagggcacc cagaccgcca agctgcaggt gaccaagggc 
          781 ggccccctgc ccttcgcctg ggacatcctg tccccccagt tccagtacgg ctccaaggtg 
          841 tacgtgaagc accccgccga catccccgac tacaagaagc tgtccttccc cgagggcttc 
          901 aagtgggagc gcgtgatgaa cttcgaggac ggcggcgtgg tgaccgtgac ccaggactcc 
          961 tccctgcagg acggcacctt catctaccac gtgaagttca tcggcgtgaa cttcccctcc 
         1021 gacggccccg taatgcagaa gaagactctg ggctgggagc cctccaccga gcgcctgtac 
         1081 ccccgcgacg gcgtgctgaa gggcgagatc cacaaggcgc tgaagctgaa gggcggcggc 
         1141 cactacctgg tggagttcaa gtcaatctac atggccaaga agcccgtgaa gctgcccggc 
         1201 tactactacg tggactccaa gctggacatc acctcccaca acgaggacta caccgtggtg 
         1261 gagcagtacg agcgcgccga ggcccgccac cacctgttcc agtagcggcc gcgactctag 
         1321 atcataatca gccataccac atttgtagag gttttacttg ctttaaaaaa cctcccacac 
         1381 ctccccctga acctgaaaca taaaatgaat gcaattgttg ttgttaactt gtttattgca 
         1441 gcttataatg gttacaaata aagcaatagc atcacaaatt tcacaaataa agcatttttt 
         1501 tcactgcatt ctagttgtgg tttgtccaaa ctcatcaatg tatcttaagg cgtaaattgt 
         1561 aagcgttaat attttgttaa aattcgcgtt aaatttttgt taaatcagct cattttttaa 
         1621 ccaataggcc gaaatcggca aaatccctta taaatcaaaa gaatagaccg agatagggtt 
         1681 gagtgttgtt ccagtttgga acaagagtcc actattaaag aacgtggact ccaacgtcaa 
         1741 agggcgaaaa accgtctatc agggcgatgg cccactacgt gaaccatcac cctaatcaag 
         1801 ttttttgggg tcgaggtgcc gtaaagcact aaatcggaac cctaaaggga gcccccgatt 
         1861 tagagcttga cggggaaagc cggcgaacgt ggcgagaaag gaagggaaga aagcgaaagg 
         1921 agcgggcgct agggcgctgg caagtgtagc ggtcacgctg cgcgtaacca ccacacccgc 
         1981 cgcgcttaat gcgccgctac agggcgcgtc aggtggcact tttcggggaa atgtgcgcgg 
         2041 aacccctatt tgtttatttt tctaaataca ttcaaatatg tatccgctca tgagacaata 
         2101 accctgataa atgcttcaat aatattgaaa aaggaagagt cctgaggcgg aaagaaccag 
         2161 ctgtggaatg tgtgtcagtt agggtgtgga aagtccccag gctccccagc aggcagaagt 
         2221 atgcaaagca tgcatctcaa ttagtcagca accaggtgtg gaaagtcccc aggctcccca 
         2281 gcaggcagaa gtatgcaaag catgcatctc aattagtcag caaccatagt cccgccccta 
         2341 actccgccca tcccgcccct aactccgccc agttccgccc attctccgcc ccatggctga 
         2401 ctaatttttt ttatttatgc agaggccgag gccgcctcgg cctctgagct attccagaag 
         2461 tagtgaggag gcttttttgg aggcctaggc ttttgcaaag atcgatcaag agacaggatg 
         2521 aggatcgttt cgcatgattg aacaagatgg attgcacgca ggttctccgg ccgcttgggt 
         2581 ggagaggcta ttcggctatg actgggcaca acagacaatc ggctgctctg atgccgccgt 
         2641 gttccggctg tcagcgcagg ggcgcccggt tctttttgtc aagaccgacc tgtccggtgc 
         2701 cctgaatgaa ctgcaagacg aggcagcgcg gctatcgtgg ctggccacga cgggcgttcc 
         2761 ttgcgcagct gtgctcgacg ttgtcactga agcgggaagg gactggctgc tattgggcga 
         2821 agtgccgggg caggatctcc tgtcatctca ccttgctcct gccgagaaag tatccatcat 
         2881 ggctgatgca atgcggcggc tgcatacgct tgatccggct acctgcccat tcgaccacca 
         2941 agcgaaacat cgcatcgagc gagcacgtac tcggatggaa gccggtcttg tcgatcagga 
         3001 tgatctggac gaagagcatc aggggctcgc gccagccgaa ctgttcgcca ggctcaaggc 
         3061 gagcatgccc gacggcgagg atctcgtcgt gacccatggc gatgcctgct tgccgaatat 
         3121 catggtggaa aatggccgct tttctggatt catcgactgt ggccggctgg gtgtggcgga 
         3181 ccgctatcag gacatagcgt tggctacccg tgatattgct gaagagcttg gcggcgaatg 
         3241 ggctgaccgc ttcctcgtgc tttacggtat cgccgctccc gattcgcagc gcatcgcctt 
         3301 ctatcgcctt cttgacgagt tcttctgagc gggactctgg ggttcgaaat gaccgaccaa 
         3361 gcgacgccca acctgccatc acgagatttc gattccaccg ccgccttcta tgaaaggttg 
         3421 ggcttcggaa tcgttttccg ggacgccggc tggatgatcc tccagcgcgg ggatctcatg 
         3481 ctggagttct tcgcccaccc tagggggagg ctaactgaaa cacggaagga gacaataccg 
         3541 gaaggaaccc gcgctatgac ggcaataaaa agacagaata aaacgcacgg tgttgggtcg 
         3601 tttgttcata aacgcggggt tcggtcccag ggctggcact ctgtcgatac cccaccgaga 
         3661 ccccattggg gccaatacgc ccgcgtttct tccttttccc caccccaccc cccaagttcg 
         3721 ggtgaaggcc cagggctcgc agccaacgtc ggggcggcag gccctgccat agcctcaggt 
         3781 tactcatata tactttagat tgatttaaaa cttcattttt aatttaaaag gatctaggtg 
         3841 aagatccttt ttgataatct catgaccaaa atcccttaac gtgagttttc gttccactga 
         3901 gcgtcagacc ccgtagaaaa gatcaaagga tcttcttgag atcctttttt tctgcgcgta 
         3961 atctgctgct tgcaaacaaa aaaaccaccg ctaccagcgg tggtttgttt gccggatcaa 
         4021 gagctaccaa ctctttttcc gaaggtaact ggcttcagca gagcgcagat accaaatact 
         4081 gttcttctag tgtagccgta gttaggccac cacttcaaga actctgtagc accgcctaca 
         4141 tacctcgctc tgctaatcct gttaccagtg gctgctgcca gtggcgataa gtcgtgtctt 
         4201 accgggttgg actcaagacg atagttaccg gataaggcgc agcggtcggg ctgaacgggg 
         4261 ggttcgtgca cacagcccag cttggagcga acgacctaca ccgaactgag atacctacag 
         4321 cgtgagctat gagaaagcgc cacgcttccc gaagggagaa aggcggacag gtatccggta 
         4381 agcggcaggg tcggaacagg agagcgcacg agggagcttc cagggggaaa cgcctggtat 
         4441 ctttatagtc ctgtcgggtt tcgccacctc tgacttgagc gtcgattttt gtgatgctcg 
         4501 tcaggggggc ggagcctatg gaaaaacgcc agcaacgcgg cctttttacg gttcctggcc 
         4561 ttttgctggc cttttgctca catgttcttt cctgcgttat cccctgattc tgtggataac 
         4621 cgtattaccg ccatgcat 

    风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。

    图标文献和实验
    相关实验
    • 【求助】转染后有mRNA没有蛋白表达

      birkin 我在尝试转染某种细胞,载体是购买的商业载体pCMV6),之前转染HEK293作为预实验,已经用WB证明有效,但是换到现在这种细胞之后就很奇怪,一开始想用短期转,结果WB做不出来,觉得可能是转染率太低,于是又改做稳定转染,用了G418筛选。花了近2个月,细胞稳定下来了,取样做RT-PCR,有相当强的mRNA表达(-RT和对照组转染也做了的,基本没有带,所以不会是污染),谁知做WB还是一点东西都没有……我都快疯了,既然能抗G418,又有大量mRNA

    • 【求助】求含有CRE重组酶序列的载体

      lwjssry 求含有CRE重组酶序列的载体,有如下质粒可交换,或积分交换 表达载体: pcDNA3.1(+) pcDNA3.1/GS pcDNA4HisMax B pIRES2-EGFP pAAV-IRES-hrGFP pBudCE4.1 pEGFP-C1 pEGFP-N1 pCMV-DsRed 腺病毒载体 pADeasy-1,pShuttle,包括菌种

    • 测序通用引物

      相关专题引物设计载体 名称上游引物 ( 5'primer )下游引物( 3'primer )P3*FLAG-CMVCMV-30(825-854)CMV-24(1129-1152)pAc5.1/V5-His(_A,_B,_C)pAc5-5BGH revpAcG2TpGEX-5not availablepACTT7EEVT3/EBVrevpACT2GAL4 ADforpGAL4-ADrvpACT2p17110p12584pACYC184(BamHI-site

    图标技术资料

    暂无技术资料 索取技术资料

    同类产品报价

    产品名称
    产品价格
    公司名称
    报价日期
    ¥1000
    上海再康生物科技有限公司
    2025年11月20日询价
    ¥1000
    上海信裕生物科技有限公司
    2025年07月11日询价
    ¥800
    上海沪震实业有限公司
    2025年07月05日询价
    ¥750
    上海盖宁生物科技有限公司
    2026年03月19日询价
    ¥2000
    上海泽叶生物科技有限公司
    2025年07月11日询价
    pCMV-DsRed-Express2载体
    ¥2000