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ERCC5 antibody (AA 1136-1186)

ERCC5 Reactivity: Human IP Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7452322
  • Target See all ERCC5 Antibodies
    ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))
    Binding Specificity
    • 8
    • 6
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1136-1186
    Reactivity
    • 40
    • 13
    • 12
    • 4
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 36
    • 4
    Rabbit
    Clonality
    • 37
    • 3
    Polyclonal
    Conjugate
    • 28
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ERCC5 antibody is un-conjugated
    Application
    • 30
    • 14
    • 8
    • 6
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Immunoprecipitation (IP)
    Purpose
    Rabbit anti-ERCC5/XPG Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogen
    between AA 1136 and 1186
    Isotype
    IgG
    Top Product
    Discover our top product ERCC5 Primary Antibody
  • Application Notes

    IP: 2 - 5 μg/mg lysate

    WB: Not recommended. Use rabbit anti-ERCC5/XPG antibody ABIN7453883.

    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
    ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))
    Alternative Name
    ERCC5/XPG (ERCC5 Products)
    Background
    Background: ERCC5 is a single-stranded DNA endonuclease involved in DNA excision repair. ERCC5 is an important component of the nucleotide excision repair (NER) pathway which is critical to the repair of DNA lesions caused by exposure to UV light. Defects in ERCC5 are the cause of xeroderma pigmentosum, an autosomal recessive disease characterized by a hypersensitivity to sunlight and a high predisposition to cancer on UV-exposed areas.
    Gene ID
    2073
    NCBI Accession
    NP_000114
    UniProt
    P28715
    Pathways
    DNA Damage Repair
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