製品の概要

製品の詳細

  • 由来
    Recombinant
  • 由来
    Escherichia coli
  • アミノ酸配列
    • アクセッション番号
    • 生物種
      Human
    • 配列
      MGSSHHHHHH SSGLVPRGSH MSTEGGGRRC QAQVSRRISF SASHRLYSKF LSDEENLKLF GKCNNPNGHG HNYKVVVTVH GEIDPATGMV MNLADLKKYM EEAIMQPLDH KNLDMDVPYF ADVVSTTENV AVYIWDNLQK VLPVGVLYKV KVYETDNNIV VYKGE.
    • 分子量
      19 kDa including tags
    • 領域
      1 to 145
    • タグ
      His tag N-Terminus

特性

Our Abpromise guarantee covers the use of ab116410 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

  • 精製度
    > 95 % SDS-PAGE.
    ab116410 was purified by proprietary chromatographic techniques and filter sterilized.
  • 製品の状態
    Liquid
  • 備考
    Although stable at 4°C for 4 weeks, ab116410 should be stored desiccated below -18°C. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Please prevent freeze-thaw cycles.
  • Concentration information loading...

前処理および保存

  • 保存方法および安定性

    Shipped at 4°C. Please see notes section.

    pH: 8.00
    Constituents: 20% Glycerol, 0.32% Tris HCl, 0.02% DTT

関連情報

  • 別名
    • 6 pyruvoyl tetrahydrobiopterin synthase
    • 6 pyruvoyl tetrahydropterin synthase
    • 6 pyruvoyltetrahydropterin synthase
    • 6-pyruvoyl tetrahydrobiopterin synthase
    • EC 4.2.3.12
    • FLJ97081
    • OTTHUMP00000235385
    • PTP synthase
    • PTPS
    • PTPS_HUMAN
    • PTS
    see all
  • 機能
    Involved in the biosynthesis of tetrahydrobiopterin, an essential cofactor of aromatic amino acid hydroxylases. Catalyzes the transformation of 7,8-dihydroneopterin triphosphate into 6-pyruvoyl tetrahydropterin.
  • パスウェイ
    Cofactor biosynthesis; tetrahydrobiopterin biosynthesis; tetrahydrobiopterin from 7,8-dihydroneopterin triphosphate: step 1/3.
  • 関連疾患
    Defects in PTS are the cause of BH4-deficient hyperphenylalaninemia type A (HPABH4A) [MIM:261640]; also called 6-pyruvoyl-tetrahydropterin synthase deficiency (PTS deficiency) or hyperphenylalaninemia tetrahydrobiopterin-deficient due to PTS deficiency. HPABH4A is an autosomal recessive disorder characterized by depletion of the neurotransmitters dopamine and serotonin, and clinically by severe neurological symptoms unresponsive to the classic phenylalanine-low diet.
  • 配列類似性
    Belongs to the PTPS family.
  • 翻訳後修飾
    Phosphorylation of Ser-19 is required for maximal enzyme activity.
  • Information by UniProt

Recombinant Human PTS protein (ab116410) 使用論文

ab116410 has not yet been referenced specifically in any publications.

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