DDB1-Polyclonal Antibodies

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DDB1

Qty


Total
$220
Catalog #
A2896
Antibody Type
Polyclonal Antibody
Gene ID
1642
Swiss Prot
Q16531
Size
Species
Rabbit
Isotype
IgG
Purity
Affinity purification
Additional Information
ReactivityHuman Mouse Rat
Tested applicationsWB IHC
Recommended DilutionWB 1:500 - 1:1000 IHC 1:50 - 1:100
Calculated MW127kDa
Observed MWRefer to Figures
ImmunogenA synthetic peptide of human DDB1
Storage BufferStore at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Concentratione
SynonymXPE;DDBA;XAP1;XPCE;XPE-BF;UV-DDB1;
Images
  • A2896: image 1

    Western blot analysis of extracts of various cell lines, using DDB1 antibody.

  • A2896: image 2

    Immunohistochemistry of paraffin-embedded human cervical cancer tissue using DDB1 antibody.

  • A2896: image 3

    Immunohistochemistry of paraffin-embedded human metrocarcinoma using DDB1 antibody at dilution of 1:200 (400x lens).

  • A2896: image 4

    Immunohistochemistry of paraffin-embedded mouse testis using DDB1 antibody at dilution of 1:200 (400x lens).

  • A2896: image 5

    Immunohistochemistry of paraffin-embedded human liver injury using DDB1 antibody at dilution of 1:200 (400x lens).

  • A2896: image 6

    Immunohistochemistry of paraffin-embedded human kidney cancer using DDB1 antibody at dilution of 1:200 (400x lens).

  • A2896: image 7

    Immunohistochemistry of paraffin-embedded human stomach cancer using DDB1 antibody at dilution of 1:200 (400x lens).

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.

Protocol

N/A

MSDS
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