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WNK1 anticorps (AA 1625-1675)

L’anticorps Lapin Polyclonal anti-WNK1 a été validé pour WB et IP. Il convient pour détecter WNK1 dans des échantillons de Humain.
N° du produit ABIN7452167

Aperçu rapide pour WNK1 anticorps (AA 1625-1675) (ABIN7452167)

Antigène

Voir toutes WNK1 Anticorps
WNK1 (WNK Lysine Deficient Protein Kinase 1 (WNK1))

Reactivité

  • 68
  • 42
  • 39
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 83
  • 1
Lapin

Clonalité

  • 74
  • 10
Polyclonal

Conjugué

  • 33
  • 5
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp WNK1 est non-conjugé

Application

  • 29
  • 27
  • 23
  • 13
  • 13
  • 10
  • 6
  • 5
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • Épitope

    • 15
    • 11
    • 6
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1625-1675

    Fonction

    Rabbit anti-WNK1 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogène

    between AA 1625 and 1675

    Isotype

    IgG
  • Indications d'application

    IP: 2 - 5 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C

    Date de péremption

    12 months
  • Antigène

    WNK1 (WNK Lysine Deficient Protein Kinase 1 (WNK1))

    Autre désignation

    WNK1

    Sujet

    Background: WNK1 (with no lysine 1) is a member of the WNK family of serine-threonine kinases. The WNK family of kinases has been observed to play a role in several cellular processes which include ion balance, signal transduction, survival, proliferation and organ development. WNK1 appears to be important to ion homeostasis. Mutations in WNK1 cause pseudohypoaldosteronism type II (PHA II), also called Gordon's syndrome, an autosomal dominant disease characterized by defects in ion transport in the nephron that result in hypertension and hyperkalemia. WNK1 has been reported to regulate sodium and chloride ion transport by influencing the activity of another WNK family member, WNK4. WNKF1 has also been observed to regulate ion homeostasis independent of WNK4.

    ID gène

    65125

    NCBI Accession

    NP_061852

    UniProt

    Q9H4A3
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