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DDB1 antibody (AA 749-1123)

The Rabbit Polyclonal anti-DDB1 antibody has been validated for WB, IHC and IF. It is suitable to detect DDB1 in samples from Human.
Catalog No. ABIN1886645

Quick Overview for DDB1 antibody (AA 749-1123) (ABIN1886645)

Target

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

Reactivity

  • 45
  • 24
  • 20
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

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
  • 15
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  • 9
  • 4
  • 2
  • 2
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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 8
    • 5
    • 2
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    • 2
    • 1
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    • 1
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    AA 749-1123

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 749 and 1123 of DDB1
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.50-1.500
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

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

    Alternative Name

    DDB1

    Background

    This gene encodes the large subunit of DNA damage-binding protein which is a heterodimer composed of a large and a small subunit.This protein functions in nucleotide-excision repair.Its defective activity causes the repair defect in the patients with xeroderma pigmentosum complementation group E (XPE).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.[provided by RefSeq]

    Molecular Weight

    127 kDa

    Gene ID

    1642

    NCBI Accession

    NM_001923, NP_001914

    Pathways

    DNA Damage Repair
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