Leadgene Leadgene
LeadGMP® T7 RNA Polymerase
カタログ番号

LDG005R-GMP

その他のドキュメント
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  • 概要

    説明

    Bacteriophage T7 RNA Polymerase is a DNA-dependent RNA polymerase with high specificity for the T7 promoter. This enzyme catalyzes the 5’→3’ synthesis of RNA from DNA downstream from its promoter.

    コンポーネント

    Package

    Items

    Quantity

    25,000 U

    T7 RNA Polymerase (200 U/μL)

    1 vial (25,000 U)

    10× RNA Polymerase reaction buffer

    1 vial (1 mL)

    100 mM DTT

    1 vial (1 mL)

    200,000 U

    T7 RNA Polymerase (200 U/μL)

    1 vial (200,000 U)

    10× RNA Polymerase reaction buffer

    1 vial (4 mL)

    100 mM DTT

    1 vial (4 mL)

    2,000,000 U

    T7 RNA Polymerase (200 U/μL)

    1 vial (2,000,000 U)

    10× RNA Polymerase reaction buffer

    1 vial (40 mL)

    100 mM DTT

    1 vial (40 mL)

    • 25,000 U

      Items

      T7 RNA Polymerase (200 U/μL)

      Quantity

      1 vial (25,000 U)

      Items

      10× RNA Polymerase reaction buffer

      Quantity

      1 vial (1 mL)

      Items

      100 mM DTT

      Quantity

      1 vial (1 mL)

    • 200,000 U

      Items

      T7 RNA Polymerase (200 U/μL)

      Quantity

      1 vial (200,000 U)

      Items

      10× RNA Polymerase reaction buffer

      Quantity

      1 vial (4 mL)

      Items

      100 mM DTT

      Quantity

      1 vial (4 mL)

    • 2,000,000 U

      Items

      T7 RNA Polymerase (200 U/μL)

      Quantity

      1 vial (2,000,000 U)

      Items

      10× RNA Polymerase reaction buffer

      Quantity

      1 vial (40 mL)

      Items

      100 mM DTT

      Quantity

      1 vial (40 mL)

  • 仕様
    • 発現系

      Escherichia coli

      保存バッファー

      T7 RNA Polymerase is supplied in 100 mM Tris-HCl (pH 7.9), 20 mM KCl, 1 mM DTT, 1 mM EDTA, 0.1% Triton® X-100 and 50% (v/v) glycerol.

    • 純度

      >98% as determined by SDS-PAGE analysis.

      単位定義

      One unit is defined as the amount of the enzyme incorporates 1 nmol of ATP into acid-insoluble product in 1 hour at 37°C.

    • 反応条件

      1× RNA Polymerase Reaction Buffer, supplemented with 0.5 mM each ATP, UTP, GTP, CTP, and DNA template containing the T7 RNA Polymerase promoter. Incubate at 37°C.
      10× RNA Polymerase Reaction Buffer: 400 mM Tris-HCl (pH 8.0), 60 mM MgCl₂, and 20 mM spermidine.

      エンドトキシン量

      <0.05 EU per 1 µg of the protein by the LAL method.

    • マイコプラズマ

      Not detected

  • 使用説明
    • 配送

      The product is shipped with polar packs. Upon receipt, store it immediately at -20°C or lower for long term storage.

      安定性および保存

      This product is stable after storage at:

      • -20°C or -80°C for 12 months under sterile conditions from date of receipt.
      • For optimal storage, aliquot the enzyme, reaction buffer and DTT reagent into smaller quantities and store at recommended temperature.
      • For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
    • 製造仕様

      LeadGMP® recombinant proteins are manufactured in ISO 13485:2016 and GMP certified facility. The processes include:

      • Animal-free reagent and laboratory
      • Manufactured and tested under GMP guideline
      • Testing and traceability of raw material
      • Records of the maintenance and equipment calibration
      • Personnel training records
      • Batch-to-batch consistency
      • Documentation of QA control and process changes
      • Manufactured and tested under an ISO 13485:2016 certified quality management system
      • Stability monitor of product shelf-life
  • 画像
    SDS-PAGE analysis of recombinant T7 RNA Polymerase.

    SDS-PAGE analysis of recombinant T7 RNA Polymerase.

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    合計   (1)
  • レビュー

    この製品についてのご経験を共有してください。下のリンクから投稿いただけます。

  • 論文

    現在論文はありません。下のリンクからお知らせください。

  • データシート & ドキュメント
    MSDS
    マニュアル
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免責事項:For Research Use or Further Manufacturing Only.

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