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ASL anticorps (AA 86-335)

L’anticorps Lapin Polyclonal anti-ASL a été validé pour WB et IHC. Il convient pour détecter ASL dans des échantillons de Humain.
N° du produit ABIN1886687

Aperçu rapide pour ASL anticorps (AA 86-335) (ABIN1886687)

Antigène

Voir toutes ASL Anticorps
ASL (Argininosuccinate Lyase (ASL))

Reactivité

  • 58
  • 15
  • 11
  • 6
  • 6
  • 6
  • 6
  • 6
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
Humain

Hôte

  • 53
  • 5
Lapin

Clonalité

  • 55
  • 3
Polyclonal

Conjugué

  • 29
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ASL est non-conjugé

Application

  • 39
  • 13
  • 13
  • 12
  • 11
  • 11
  • 7
  • 6
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Épitope

    • 15
    • 11
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 86-335

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 86 and 335 of Human ASL
  • Indications d'application

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.50-1.500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Antigène

    ASL (Argininosuccinate Lyase (ASL))

    Autre désignation

    Argininosuccinate Lyase

    Sujet

    This gene encodes a member of the lyase 1 family.The encoded 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 this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.A nontranscribed pseudogene is also located on the long arm of chromosome 22.Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq]

    Poids moléculaire

    49 kDa

    ID gène

    435

    NCBI Accession

    NP_001020117, NM_001024946

    Pathways

    Response to Growth Hormone Stimulus
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