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EC300110

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  • 询价
  • Epicentre已认证
  • EC300105,EC300110,EC300150
  • USA
  • 2026年01月02日
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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 供应商

      北京中北林格科技发展有限公司

    • 英文名

      TransforMax™ EPI300™ Electrocompetent E. coli

    • 库存

      大量

    • 保存条件

      -70℃

    TransforMax™ EPI300™ Electrocompetent E. coli
    TransforMax™ EPI300™ Chemically Competent E. coli

    欢迎来电询价订购

    电话:010-88891086(806)

    联系人:康 乐

    TransforMax™ EPI300™ E. coli cells lack the tonA gene and are engineered for use with EPICENTRE's CopyControl™ cDNA, Gene, and PCR Cloning Kit and other CopyControl Cloning Systems* that do not require phage T1-resistant cells. The cells contain an inducible mutant trfA gene whose gene product is required for initiation of replication from the oriV origin of replication, such as that in CopyControl pCC1™ vectors or in clones that are retrofitted with CopyControl capability using the EZ-Tn5™< oriV/KAN-2> Insertion Kit. On LB chloramphenicol plates or in LB or SOC media supplemented with chloramphenicol, CopyControl clones grown in TransforMax EPI300 E. coli replicate at single-copy number from the F-factor replicon because expression of the trfA gene is repressed. Addition of CopyControl Induction Solution induces the cells to express the trfA gene product and induces their replication at high-copy number from oriV (Fig. 1). Replication from oriV results in higher yields and higher purity of cloned DNA.

    Benefits

    • Copy-number of clones is under tight control of an inducible promoter linked to the trfA gene.
    • High transformation efficiency with clones of all sizes.
    • lacZΔM15 for blue/white screening of recombinants.
    • Restriction-minus [mcrA, Δ(mrr-hsdRMS-mcrBC)] phenotype enables efficient cloning of methylated DNA.
    • Endonuclease-minus (endA1), to ensure high yields of DNA.
    • Recombination-minus (recA1), for greater stability of large insert clones.

    Figure 1

    Figure 1. Copy number of CopyControl™ BAC clones can be induced 10- to 20-fold in TransforMax™ EPI300™ E. coli. The yield of BAC DNA from CopyControl BAC clones of 110-145 kb increased >14-fold following addition of CopyControl Induction Solution. U=uninduced cells; I=induced cells.

    Genotype

    F- mcrA Δ(mrr-hsdRMS-mcrBC) Φ80dlacZΔM15 ΔlacX74 recA1 endA1 araD139 Δ(ara, leu)7697 galU galK λ- rpsL (StrR) nupG trfA dhfr

    TransforMax EPI300 Electrocompetent E. coli

    • Transformation efficiency of >1 x 1010 cfu/µg of pUC19.

    TransforMax EPI300 Chemically Competent E. coli

    • Transformation efficiency of >5 x 108 cfu/µg of pUC19.



    ZhongBei LinGe Biotechnology Ltd.
    Room C, Building W48, Longcheng Huayuan Mansion
    Changping District
    Beijing 102208, China
    Tel: (8610)88891086 80794780
    Fax: (8610)80794780
    Email: bjzblg@126.com
    Web: www.bjzblg.com

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    图标文献和实验
    相关实验
    • DNA and RNA Ligases (EC 6.5.1.1, EC 6.5.1.2, and EC 6.5.1.3)

      Ligases are a class of enzymes that catalyze the joining of nucleic acid molecules by the formation of phosphodiester bonds between their termini (1 ). The nucleic acid substrate to be linked may be DNA or RNA depending on the type of ligase

    • Deoxyribonuclease I (EC 3.1.21.1) and II (EC 3.1.22.1)

      From Chapter 1 on nucleases, we know that the term DNase refers to an enzyme that endonucleolytically cleaves DNA molecules. This chapter deals with those DNases that preferentially catalyze the hydrolysis of double-stranded DNA (ds DNA

    • DNA Methyltransferases (EC 2.1.1.72 and EC 2.1.1.73)

      for one or the other base, and modify at the 6-NH2 of dA (EC 2.1.1.72) or at the N4 or 5-C position of dC (EC 2.1.1.73) depending on the particular enzyme (2 ). The reaction is predominantly irreversible. Enzymes, such as O 6 -methylguanine DNA Mtase, that participate

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