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ERCC5 antibody (N-Term)

This anti-ERCC5 antibody is a Rabbit Polyclonal antibody detecting ERCC5 in WB. Suitable for Human, Mouse and Rat.
Catalog No. ABIN631899

Quick Overview for ERCC5 antibody (N-Term) (ABIN631899)

Target

See all ERCC5 Antibodies
ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))

Reactivity

  • 43
  • 12
  • 11
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 38
  • 5
Rabbit

Clonality

  • 39
  • 4
Polyclonal

Conjugate

  • 31
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ERCC5 antibody is un-conjugated

Application

  • 32
  • 16
  • 10
  • 6
  • 6
  • 5
  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 8
    • 5
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificity

    ERCC5 antibody was raised against the N terminal of ERCC5

    Purification

    Affinity purified

    Immunogen

    ERCC5 antibody was raised using the N terminal of ERCC5 corresponding to a region with amino acids NPQAIDIESEDFSSLPPEVKHEILTDMKEFTKRRRTLFEAMPEESDDFSQ
  • Application Notes

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    ERCC5 Blocking Peptide, (ABIN5613393), is also available for use as a blocking control in assays to test for specificity of this ERCC5 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ERCC5 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))

    Alternative Name

    ERCC5

    Background

    Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage.

    Molecular Weight

    133 kDa (MW of target protein)

    Pathways

    DNA Damage Repair
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