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Recombinant Human GAMT protein (ab185414)

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Key features and details

  • Expression system: Escherichia coli
  • Purity: > 95% SDS-PAGE
  • Endotoxin level: < 1.000 Eu/ng
  • Tags: His tag C-Terminus, His tag N-Terminus
  • Suitable for: SDS-PAGE, HPLC

製品の詳細

  • 製品名

    Recombinant Human GAMT protein
    GAMT タンパク質・ペプチド 製品一覧

  • 精製度

    > 95 % SDS-PAGE.
    Purity is determined by SEC-HPLC and reducing SDS-PAGE.

  • エンドトキシン・レベル

    < 1.000 Eu/ng

  • 発現系

    Escherichia coli

  • アクセッション番号

    Q14353

  • タンパク質長

    Full length protein

  • Animal free

    No

  • 由来

    Recombinant

    • 生物種

      Human

    • 配列

      MGSSHHHHHHSSGLVPRGSHMSAPSATPIFAPGENCSPAWGAAPAAYDAA DTHLRILGKPVMERWETPYMHALAAAASSKGGRVLEVGFGMAIAASKVQE APIDEHWIIECNDGVFQRLRDWAPRQTHKVIPLKGLWEDVAPTLPDGHFD GILYDTYPLSEETWHTHQFNFIKNHAFRLLKPGGVLTYCNLTSWGELMKS KYSDITIMFEETQVPALLEAGFRRENIRTEVMALVPPADCRYYAFPQMIT PLVTKGLEHH HHHH

    • 予測される分子量

      30 kDa including tags

    • 領域

      1 to 236

    • タグ

      His tag C-Terminus , His tag N-Terminus

特性

Our Abpromise guarantee covers the use of ab185414 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • アプリケーション

    SDS-PAGE

    HPLC

  • 製品の状態

    Liquid
  • Concentration information loading...

前処理および保存

  • 保存方法および安定性

    Shipped on Dry Ice. Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle.

    pH: 8.00
    Constituents: 0.32% Tris HCl, 0.02% DTT

関連情報

  • 別名

    • CCDS2
    • Epididymis secretory protein Li 20
    • GAMT
    • GAMT_HUMAN
    • Guanidinoacetate N methyltransferase
    • Guanidinoacetate N-methyltransferase
    • HEL-S-20
    • PIG2
    • TP53I2
    see all

  • 組織特異性

    Expressed in liver.

  • パスウェイ

    Amine and polyamine biosynthesis; creatine biosynthesis; creatine from L-arginine and glycine: step 2/2.

  • 関連疾患

    Defects in GAMT are the cause of guanidinoacetate methyltransferase deficiency (GAMT deficiency) [MIM:612736]. GAMT deficiency is an autosomal recessive disorder characterized by developmental delay/regression, mental retardation, severe disturbance of expressive and cognitive speech, intractable seizures and movement disturbances, severe depletion of creatine/phosphocreatine in the brain, and accumulation of guanidinoacetic acid (GAA) in brain and body fluids.

  • 配列類似性

    Belongs to the RMT2 methyltransferase family.
  • Information by UniProt

プロトコール

To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

Click here to view the general protocols

参考文献 (0)

ab185414 を使用した論文を発表された方は、こちらまでお知らせください。データシートに掲載させていただきます。

ab185414 は論文での使用が確認できていません。

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