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WNK1 antibody (AA 1625-1675)

The Rabbit Polyclonal anti-WNK1 antibody has been validated for WB and IP. It is suitable to detect WNK1 in samples from Human.
Catalog No. ABIN7452167

Quick Overview for WNK1 antibody (AA 1625-1675) (ABIN7452167)

Target

See all WNK1 Antibodies
WNK1 (WNK Lysine Deficient Protein Kinase 1 (WNK1))

Reactivity

  • 71
  • 44
  • 41
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 86
  • 1
Rabbit

Clonality

  • 75
  • 12
Polyclonal

Conjugate

  • 36
  • 5
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This WNK1 antibody is un-conjugated

Application

  • 31
  • 29
  • 25
  • 13
  • 13
  • 11
  • 6
  • 5
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • Binding Specificity

    • 15
    • 12
    • 6
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1625-1675

    Purpose

    Rabbit anti-WNK1 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 1625 and 1675

    Isotype

    IgG
  • Application Notes

    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

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    4 °C

    Expiry Date

    12 months
  • Target

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

    Alternative Name

    WNK1

    Background

    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.

    Gene ID

    65125

    NCBI Accession

    NP_061852

    UniProt

    Q9H4A3
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