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Turbo核酸酶

Turbo核酸酶,Turbo Nuclease,也称为Benzonase®,粘质沙雷氏菌,重组,大肠杆菌。更多视频请关注视频号【艾维缔】。哔哩哔哩【IVDSHOW】。抖音【军哥聊表观】。


关键词

Turbo核酸酶


所属分类


目录号

EN180

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  • For general laboratory use.

    Please centrifuge briefly before opening (volume ≤2 ml).

    Unit Definition: One unit will digest sonicated salmon sperm DNA to acid-soluble oligonucleotides equivalent to a Δ260 of 1.0 in 30 min at pH 8.0 at 37 °C.

    Shipping: shipped on gel packs

    Storage Conditions: store at -20 °C
    avoid freeze/thaw cycles

    Shelf Life: 12 months

    Form: liquid (Supplied in 20 mM Tris-HCl pH 8.0, 20 mM NaCl, 2 mM MgCl2, 1 mM DTT and 50 % [v/v] glycerol)

    Concentration: 250 units/μl

    Applications:
    Turbo Nuclease is very effective in degrading nucleic acid from protein samples and it is used in a variety of application where complete hydrolysis of DNA/RNA is required:

    • Reduction of viscosity from cell lysates
    • Prevention of cell clumping
    • Elimination of unspecific protein-DNA complexes prior 2D- or native gel electrophoresis
    • Removal of nucleic acids from large-scale protein preparations

    Description:
    Turbo Nuclease is a broad-spectrum endonuclease that cleaves both DNA and RNA molecules independently of being single- or double-stranded, circular, linear or supercoiled. The enzyme is highly stable and active in a broad range of pH and temperature, making it ideal for a variety of downstream processes that require the degradation of DNA/RNA in a simple, efficient and specific manner.

    • Endonuclease from Serratia macescens recombinant expressed and purified from E. coli
    • Catalytic activity from pH 6 to 10 (optimal around 8.8) and temperature 0 to 44 °C
    • High catalytic efficiency (34-fold greater than DNase I)
    • Activity requires the presence of Mg2+ (optimum 2 mM)

    Procedure:

    • Make a fresh, cold lysis buffer in which the target protein is soluble and is compatible with downstream purification processes, e.g. minimal amount of EDTA or DTT if a Ni-NTA column will be used.
    • Resuspend the thawed cell paste in lysis buffer. Use 2-10 ml Lysis Buffer for each gram of cell paste.
    • Add Turbo Nuclease to 2.5 units/ml.
    • A fluid 'aqueous' solution will result after 15 min.
  • 产品组分

    内容

    型号

    规格

    储存温度

    Turbo核酸酶

    EN180-01

    10000Units

    -20°C

    Turbo核酸酶

    EN180-02

    50000Units

    -20°C

    操作手册

    1 1

    常温

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    EN180-Turbo核酸酶

    操作手册

    EN180-Turbo核酸酶相关单页

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  • 注意事项

    保存建议厂家推荐蓝冰运输。当您收到产品后,按照说明书建议保存于-20°C。

     

  • FAQ

  • Mass spectrometry reveals novel features of tubulin polyglutamylation in the flagellum of Trypanosoma brucei

    Nisavic Marija, Chaze Thibault, ..., Chamot-Rooke Julia

    bioRxiv  |  2025 Feb 06

    Features of membrane protein sequence direct post-translational insertion.

    Ilya A Kalinin, Hadas Peled-Zehavi, ..., Nir Fluman

    Nature communications  |  2024 Nov 25  |  39587101

    The long non-coding RNA FAM30A regulates the Musashi2-RUNX1 axis and is required for LSC function in AML cells

    Sánchez Jaime Calvo, Scott Mary T., ..., Köhn Marcel

    bioRxiv  |  2024 Oct 15

      Supplementary   Gentle Rhodamines for Live-Cell Fluorescence Microscopy

    Tianyan Liu, Julian Kompa, ..., Zhixing Chen

    ACS Central Science  |  2024 Oct 02

    APOBEC3C-mediated NF-κB activation enhances clear cell renal cell carcinoma progression.

    Nora Hase, Danny Misiak, ..., Marcel Köhn

    Molecular oncology  |  2024 Aug 26  |  39183666

    Biochemical and structural elucidation of the L-carnitine degradation pathway of the human pathogen Acinetobacter baumannii

    Fabian Piskol, Peer Lukat, ..., Jürgen Moser

    Frontiers in Microbiology  |  2024 Aug 14

    Rbfox1 controls alternative splicing of focal adhesion genes in cardiac muscle cells.

    Peter Zorn, Jaime Calvo Sánchez, ..., Marcel Köhn

    Journal of molecular cell biology  |  2024 Jul 01  |  38253401

    Membrane protein sequence features direct post-translational insertion

    Kalinin Ilya A., Peled-Zehavi Hadas, ..., Fluman Nir

    bioRxiv  |  2023 Dec 12

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