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DDB1 antibody

This anti-DDB1 antibody is a Rabbit Polyclonal antibody detecting DDB1 in WB and ELISA. Suitable for Human, Mouse and Rat.
Catalog No. ABIN7237955

Quick Overview for DDB1 antibody (ABIN7237955)

Target

See all DDB1 Antibodies
DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))

Reactivity

  • 45
  • 23
  • 19
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 37
  • 7
  • 1
Rabbit

Clonality

  • 35
  • 10
Polyclonal

Conjugate

  • 34
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DDB1 antibody is un-conjugated

Application

  • 30
  • 16
  • 14
  • 14
  • 11
  • 10
  • 9
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Synthetic peptide of human DDB1

    Isotype

    IgG
  • Application Notes

    WB 1:200-1:500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.3 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))

    Alternative Name

    DDB1

    Background

    The protein encoded by this gene is the large subunit (p127) of the heterodimeric DNA damage-binding (DDB) complex while another protein (p48) forms the small subunit. This protein complex functions in nucleotide-excision repair and binds to DNA following UV damage. Defective activity of this complex causes the repair defect in patients with xeroderma pigmentosum complementation group E (XPE) - an autosomal recessive disorder characterized by photosensitivity and early onset of carcinomas. However, it remains for mutation analysis to demonstrate whether the defect in XPE patients is in this gene or the gene encoding the small subunit. In addition, Best vitelliform mascular dystrophy is mapped to the same region as this gene on 11q, but no sequence alternations of this gene are demonstrated in Best disease patients. The protein encoded by this gene also functions as an adaptor molecule for the cullin 4 (CUL4) ubiquitin E3 ligase complex by facilitating the binding of substrates to this complex and the ubiquitination of proteins.

    Molecular Weight

    127 kDa

    NCBI Accession

    NP_001914

    UniProt

    Q16531

    Pathways

    DNA Damage Repair
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