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Argininosuccinate Lyase (ASL) Peptide

ASL Reactivité: Mammifères Hôte: Synthetic BP, WB, IHC
N° du produit ABIN938561
  • Antigène Tous les produits ASL
    ASL (Argininosuccinate Lyase (ASL))
    Type de proteíne
    Synthetic
    Origine
    Mammifères
    Source
    • 4
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Séquence
    GATAGKLHTG RSRNDQVVTD LRLWMRQTCS TLSGLLWELI RTMVDRAEAE
    Attributs du produit
    A synthetic peptide for use as a blocking control in assays to test for specificity of ASL antibody,
    Alternative Names: ASL control peptide, ASL antibody Blocking Peptide, Anti-ASL Blocking Peptide, Argininosuccinate Lyase Blocking Peptide, ASAL Blocking Peptide
  • Indications d'application
    Optimal conditions should be determined by the investigator
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20 °C long term.
  • Antigène
    ASL (Argininosuccinate Lyase (ASL))
    Synonymes
    ASAL Peptide, 2510006M18Rik Peptide, zgc:63532 Peptide, BA4879 Peptide, PSPTO0125 Peptide, Adl Peptide, Asl Peptide, argininosuccinate lyase Peptide, argininosuccinate lyase ArgH Peptide, adenylosuccinate lyase Peptide, argininosuccinate lyase L homeolog Peptide, ASL Peptide, Asl Peptide, asl Peptide, argH2 Peptide, argH Peptide, arg7 Peptide, CNC04420 Peptide, STHERM_c13370 Peptide, Adsl Peptide, asl.L Peptide, ARG7 Peptide
    Sujet
    ASL is a member of the lyase 1 family. The protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in its gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.
    Poids moléculaire
    52 kDa
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