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pUC19 Plasmid

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  • 2025年09月20日
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    • 文献和实验
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    • 保存条件

      负20摄氏度

    • 保质期

      3个月

    • 英文名

      pUC19

    • 库存

      50

    • 供应商

      LSMBIO

    • 规格

      2ug

    pUC19

    Search name

    pUC19,Plasmid pUC19,pUC19 vector

     

    pUC19 Information

    Promoter: Lac/lac promoter

    Replicon: ColE1 ori

    Plasmid classification: Escherichia coli vector; cloned plasmid

    Plasmid size: 2686bp

    Plasmid label: LacZ

    Prokaryotic resistance: ampicillin Amp

    Cloned strain: DH5 alpha

    Culture conditions: 37 centigrade, aerobic, LB

    5'sequencing primers: M13F:TGTAAAACGACGGCCAGT

    3'sequencing primers: M13R:CAGGAAACAGCTATGACC

    Note: selection of blue leukoplakia

     

    pUC19 Description

    The size of pUC18 and pUC19 is only 2686bp, the most commonly used plasmid vector with compact structure, almost free of excess DNA, and GenBank registration number of L08752 (pUC18) and X02514 (pUC19). From pBR322, lacZ (MSC) comes from M13mp18/19. The structure of these two plasmids is almost the same, but the direction of the polyclonal sites is opposite. These plasmids lack ROP gene that controls copy number, so the copy number is 500-700. The pUC series contains a partial coding sequence of the amino terminal of a lacZ protein, which can exhibit alpha complementarity in specific receptor cells. Therefore, after inserting foreign fragments into polyclonal sites, the recombinant plasmids can be screened through blue and white colonies formed by alpha complementarity. PUC18 and pUC19 vectors are suitable for cloning DNA fragments, sequencing DNA, and expressing foreign genes. Because of the polyclonal loci in the lacZ field, it can be easily screened by blue and white to judge whether there is a DNA fragment insertion in the carrier when the lacZ deficient cell is transformed into a host (such as JM109 and so on) and is cultured on a flat medium containing IPTG and X-Gal. At the same time, foreign genes can be expressed by lac promoter on the vector, and DNA fragments in insertion vectors can be sequenced. DNA sequencing can facilitate the use of M13 universal primers.

     

    pUC19 Multiple site

    pUC19-multiple-site

     

    pUC19 Sequence

    LOCUS       Exported File           2686 bp ds-DNA    circular SYN 02-2-2015
    KEYWORDS    pUC19
    SOURCE      synthetic DNA construct
      ORGANISM  synthetic DNA construct
    REFERENCE   1  (bases 1 to 2686)
      AUTHORS   .
      TITLE     Direct Submission
      JOURNAL   Exported 2015-2-2  
    FEATURES             Location/Qualifiers
         source          1..2686
                         /organism="synthetic DNA construct"
                         /mol_type="other DNA"
         protein_bind    106..127
                         /bound_moiety="E. coli catabolite activator protein"
                         /note="CAP binding site"
                         /note="CAP binding activates transcription in the presence
                         of cAMP."
         promoter        142..172
                         /note="lac promoter"
                         /note="promoter for the E. coli lac operon"
         protein_bind    180..196
                         /bound_moiety="lac repressor encoded by lacI"
                         /note="lac operator"
                         /note="The lac repressor binds to the lac operator to
                         inhibit transcription in E. coli. This inhibition can be
                         relieved by adding lactose or
                         isopropyl-beta-D-thiogalactopyranoside (IPTG)."
         primer_bind     204..220
                         /note="M13 rev"
                         /note="common sequencing primer, one of multiple similar
                         variants"
         CDS             216..539
                         /codon_start=1
                         /gene="lacZ?fragment"
                         /product="LacZ-alpha fragment of beta-galactosidase"
                         /note="lacZ-alpha"
                         /translation="MTMITPSLHACRSTLEDPRVPSSNSLAVVLQRRDWENPGVTQLNR
                         LAAHPPFASWRNSEEARTDRPSQQLRSLNGEWRLMRYFLLTHLCGISHRIWCTLSTICS
                         DAA"
         misc_feature    233..289
                         /gene="
                         "
                         /note="MCS"
                         /note="pUC18/19 multiple cloning site"
         primer_bind     complement(290..306)
                         /note="M13 fwd"
                         /note="common sequencing primer, one of multiple similar
                         variants"
         promoter        780..884
                         /gene="bla"
                         /note="AmpR promoter"
         CDS             885..1745
                         /codon_start=1
                         /gene="bla"
                         /product="beta-lactamase"
                         /note="AmpR"
                         /note="confers resistance to ampicillin, carbenicillin, and
                         related antibiotics"
                         /translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI
                         ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRIDAGQEQLGRRIHYSQNDLVEYS
                         PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW
                         EPELNEAIPNDERDTTMPVAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA
                         LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS
                         LIKHW"
         rep_origin      1916..2504
                         /direction=RIGHT
                         /note="ori"
                         /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
                         replication"
    ORIGIN
            1 gcgcccaata cgcaaaccgc ctctccccgc gcgttggccg attcattaat gcagctggca
           61 cgacaggttt cccgactgga aagcgggcag tgagcgcaac gcaattaatg tgagttagct
          121 cactcattag gcaccccagg ctttacactt tatgcttccg gctcgtatgt tgtgtggaat
          181 tgtgagcgga taacaatttc acacaggaaa cagctatgac catgattacg ccaagcttgc
          241 atgcctgcag gtcgactcta gaggatcccc gggtaccgag ctcgaattca ctggccgtcg
          301 ttttacaacg tcgtgactgg gaaaaccctg gcgttaccca acttaatcgc cttgcagcac
          361 atcccccttt cgccagctgg cgtaatagcg aagaggcccg caccgatcgc ccttcccaac
          421 agttgcgcag cctgaatggc gaatggcgcc tgatgcggta ttttctcctt acgcatctgt
          481 gcggtatttc acaccgcata tggtgcactc tcagtacaat ctgctctgat gccgcatagt
          541 taagccagcc ccgacacccg ccaacacccg ctgacgcgcc ctgacgggct tgtctgctcc
          601 cggcatccgc ttacagacaa gctgtgaccg tctccgggag ctgcatgtgt cagaggtttt
          661 caccgtcatc accgaaacgc gcgagacgaa agggcctcgt gatacgccta tttttatagg
          721 ttaatgtcat gataataatg gtttcttaga cgtcaggtgg cacttttcgg ggaaatgtgc
          781 gcggaacccc tatttgttta tttttctaaa tacattcaaa tatgtatccg ctcatgagac
          841 aataaccctg ataaatgctt caataatatt gaaaaaggaa gagtatgagt attcaacatt
          901 tccgtgtcgc ccttattccc ttttttgcgg cattttgcct tcctgttttt gctcacccag
          961 aaacgctggt gaaagtaaaa gatgctgaag atcagttggg tgcacgagtg ggttacatcg
         1021 aactggatct caacagcggt aagatccttg agagttttcg ccccgaagaa cgttttccaa
         1081 tgatgagcac ttttaaagtt ctgctatgtg gcgcggtatt atcccgtatt gacgccgggc
         1141 aagagcaact cggtcgccgc atacactatt ctcagaatga cttggttgag tactcaccag
         1201 tcacagaaaa gcatcttacg gatggcatga cagtaagaga attatgcagt gctgccataa
         1261 ccatgagtga taacactgcg gccaacttac ttctgacaac gatcggagga ccgaaggagc
         1321 taaccgcttt tttgcacaac atgggggatc atgtaactcg ccttgatcgt tgggaaccgg
         1381 agctgaatga agccatacca aacgacgagc gtgacaccac gatgcctgta gcaatggcaa
         1441 caacgttgcg caaactatta actggcgaac tacttactct agcttcccgg caacaattaa
         1501 tagactggat ggaggcggat aaagttgcag gaccacttct gcgctcggcc cttccggctg
         1561 gctggtttat tgctgataaa tctggagccg gtgagcgtgg gtctcgcggt atcattgcag
         1621 cactggggcc agatggtaag ccctcccgta tcgtagttat ctacacgacg gggagtcagg
         1681 caactatgga tgaacgaaat agacagatcg ctgagatagg tgcctcactg attaagcatt
         1741 ggtaactgtc agaccaagtt tactcatata tactttagat tgatttaaaa cttcattttt
         1801 aatttaaaag gatctaggtg aagatccttt ttgataatct catgaccaaa atcccttaac
         1861 gtgagttttc gttccactga gcgtcagacc ccgtagaaaa gatcaaagga tcttcttgag
         1921 atcctttttt tctgcgcgta atctgctgct tgcaaacaaa aaaaccaccg ctaccagcgg
         1981 tggtttgttt gccggatcaa gagctaccaa ctctttttcc gaaggtaact ggcttcagca
         2041 gagcgcagat accaaatact gttcttctag tgtagccgta gttaggccac cacttcaaga
         2101 actctgtagc accgcctaca tacctcgctc tgctaatcct gttaccagtg gctgctgcca
         2161 gtggcgataa gtcgtgtctt accgggttgg actcaagacg atagttaccg gataaggcgc
         2221 agcggtcggg ctgaacgggg ggttcgtgca cacagcccag cttggagcga acgacctaca
         2281 ccgaactgag atacctacag cgtgagctat gagaaagcgc cacgcttccc gaagggagaa
         2341 aggcggacag gtatccggta agcggcaggg tcggaacagg agagcgcacg agggagcttc
         2401 cagggggaaa cgcctggtat ctttatagtc ctgtcgggtt tcgccacctc tgacttgagc
         2461 gtcgattttt gtgatgctcg tcaggggggc ggagcctatg gaaaaacgcc agcaacgcgg
         2521 cctttttacg gttcctggcc ttttgctggc cttttgctca catgttcttt cctgcgttat
         2581 cccctgattc tgtggataac cgtattaccg cctttgagtg agctgatacc gctcgccgca
         2641 gccgaacgac cgagcgcagc gagtcagtga gcgaggaagc ggaaga
    //

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    图标文献和实验
    该产品被引用文献
    Structural basis for the interaction of the chaperone Cbp3 with newly synthesized cytochrome b during mitochondrial respiratory chain assembly Mama Ndi1, Geoffrey Masuyer1, Hannah Dawitz1, Andreas Carlstr?m1, Mirco Michel1, Arne Elofsson2, Mikaela Rapp1, P?l Stenmark3 and Martin Ott3* First Published on Journal of biological chemistry September 19, 2019 doi: 10.1074/jbc.RA119.010483 jbc.RA119.010483.
    相关实验
    • pUC18 和 pUC19质粒图谱

      相关专题 那些实验室常用的克隆载体 pUC18 和 pUC19质粒图谱 pUC18 和 pUC19 大小只有 2686bp ,是最常用的质粒载体,其结构组成紧凑,几乎不含多余的 DNA 片段,GenBank注册号为 L08752(pUC18)和 X02514(pUC19)。由 pBR322 改造而来,其中 lacZ (MSC)来自 M13mp18/19 图 3-4 是其质粒图谱 。 这两个质粒的结构几乎是完全一样的,只是多克隆位点的排列方向相反。这些质粒缺乏控制拷贝数的 rop 基因

    • pUC18 和 pUC19质粒图谱

      相关专题 那些实验室常用的克隆载体 pUC18 和 pUC19质粒图谱 pUC18 和 pUC19 大小只有 2686bp ,是最常用的质粒载体,其结构组成紧凑,几乎不含多余的 DNA 片段,GenBank注册号为 L08752(pUC18)和 X02514(pUC19)。由 pBR322 改造而来,其中 lacZ (MSC)来自 M13mp18/19 图 3-4 是其质粒图谱 。 这两个质粒的结构几乎是完全

    • pUC18 和 pUC19质粒图谱

      相关专题 那些实验室常用的克隆载体 pUC18 和 pUC19质粒 图谱 pUC18 和 pUC19 大小只有 2686bp ,是最常用的质粒载体 ,其结构组成紧凑,几乎不含多余的 DNA 片段,GenBank注册号为 L08752(pUC18)和 X02514(pUC19)。由 pBR322 改造而来,其中 lacZ (MSC)来自 M13mp18/19 图 3-4 是其质粒图谱。 这两个质粒的结构几乎

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