Recombinant Human Argininosuccinate Lyase protein (ab113605)

製品の概要

  • 製品名
    Recombinant Human Argininosuccinate Lyase protein
  • タンパク質長
    Full length protein

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
      MGSSHHHHHHSSGLVPRGSHMASESGKLWGGRFVGAVDPIMEKFNASIAY DRHLWEVDVQGSKAYSRGLEKAGLLTKAEMDQILHGLDKVAEEWAQGTFK LNSNDEDIHTANERRLKELIGATAGKLHTGRSRNDQVVTDLRLWMRQTCS TLSGLLWELIRTMVDRAEAERDVLFPGYTHLQRAQPIRWSHWILSHAVAL TRDSERLLEVRKRINVLPLGSGAIAGNPLGVDRELLRAELNFGAITLNSM DATSERDFVAEFLFWASLCMTHLSRMAEDLILYCTKEFSFVQLSDAYSTG SSLMPQKKNPDSLELIRSKAGRVFGRCAGLLMTLKGLPSTYNKDLQEDKE AVFEVSDTMSAVLQVATGVISTLQIHQENMGQALSPDMLATDLAYYLVRK GMPFRQAHEASGKAVFMAETKGVALNQLSLQELQTISPLFSGDVICVWDY GHSVEQYGALGGTARSSVDWQIRQVRALLQAQQA
    • 分子量
      54 kDa including tags
    • 領域
      1 to 464
    • タグ
      His tag N-Terminus

特性

Our Abpromise guarantee covers the use of ab113605 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.
    ab113605 was purified using conventional chromatography techniques.
  • 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 at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.32% Tris HCl, 0.04% DTT, 10% Glycerol, 0.58% Sodium chloride

関連情報

  • 別名
    • Argininosuccinase
    • Argininosuccinate lyase
    • Arginosuccinase
    • ARLY_HUMAN
    • ASAL
    • ASL
    • EC 4.3.2.1
    see all
  • パスウェイ
    Amino-acid biosynthesis; L-arginine biosynthesis; L-arginine from L-ornithine and carbamoyl phosphate: step 3/3.
    Nitrogen metabolism; urea cycle; L-arginine and fumarate from (N(omega)-L-arginino)succinate: step 1/1.
  • 関連疾患
    Defects in ASL are the cause of arginosuccinicaciduria (ARGINSA) [MIM:207900]. Arginosuccinicaciduria is an autosomal recessive disorder of the urea cycle. The disease is characterized by mental and physical retardation, liver enlargement, skin lesions, dry and brittle hair showing trichorrhexis nodosa microscopically and fluorescing red, convulsions, and episodic unconsciousness.
  • 配列類似性
    Belongs to the lyase 1 family. Argininosuccinate lyase subfamily.
  • 翻訳後修飾
    Acetylation modifies enzyme activity in response to alterations of extracellular nutrient availability. Acetylation increased with trichostin A (TSA) or with nicotinamide (NAM). Glucose increases acetylation by about a factor of 3 with decreasing enzyme activity. Acetylation on Lys-288 is decreased on the addition of extra amino acids resulting in activation of enzyme activity.
  • Information by UniProt

Recombinant Human Argininosuccinate Lyase protein 画像

  • 15% SDS-PAGE showing ab113605 (3 µg) at approximately 53.8 kDa.

Recombinant Human Argininosuccinate Lyase protein (ab113605) 使用論文

ab113605 has not yet been referenced specifically in any publications.

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

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