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WRNIP1 antibody (AA 400-450)

The Rabbit Polyclonal anti-WRNIP1 antibody has been validated for WB, IP and IHC (fp). It is suitable to detect WRNIP1 in samples from Human.
Catalog No. ABIN7454746

Quick Overview for WRNIP1 antibody (AA 400-450) (ABIN7454746)

Target

See all WRNIP1 Antibodies
WRNIP1 (Werner Helicase Interacting Protein 1 (WRNIP1))

Reactivity

  • 20
  • 7
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 19
  • 1
Rabbit

Clonality

  • 20
Polyclonal

Conjugate

  • 15
  • 1
  • 1
  • 1
  • 1
  • 1
This WRNIP1 antibody is un-conjugated

Application

  • 18
  • 11
  • 6
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 9
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 400-450

    Purpose

    Rabbit anti-WRNIP1 Antibody, Affinity Purified

    Predicted Reactivity

    Mouse,Rat

    Purification

    Affinity Purified

    Immunogen

    between AA 400 and 450

    Isotype

    IgG
  • Application Notes

    IHC: 1:500 - 1:2,000. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 10 μg/mg lysate

    WB: 1:1,000 - 1:5,000

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 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

    WRNIP1 (Werner Helicase Interacting Protein 1 (WRNIP1))

    Alternative Name

    WRNIP1

    Background

    Background: WRNIP1 (Werner helicase interacting protein 1) was identified as a protein that interacts with the N-terminal region of Werner protein (WRN). WRN is a RecQ DNA helicase important to DNA repair and is the causative gene of Werner syndrome (WS), an autosomal recessive disease characterized by premature aging. WRNIP1 has been shown to interact with DNA polymerase delta (pol delta) and play a role in pol delta-mediated DNA synthesis. Additionally, WRNIP1 has been shown to interact with polyubiquitin chains indicating a link between ubiquitination and the DNA repair pathway.

    Gene ID

    56897

    NCBI Accession

    NP_064520

    UniProt

    Q96S55
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