Damage Specific DNA Binding Protein 1 (DDB1) (Middle Region) Peptide
DDB1
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all DDB1 products
- DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))
- Protein Region
- Middle Region
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Sequence
- RHVKTYEVSL REKEFNKGPW KQENVEAEAS MVIAVPEPFG GAIIIGQESI
- Characteristics
- This is a synthetic peptide designed for use in combination with anti- DDB1 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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Damage Specific DNA Binding Protein 1 (DDB1) peptide
DDB1 Reactivity: Human, Mouse, Cow, Dog, Rat Host: Synthetic BP, Imm
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- Application Notes
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))
- Synonyms
- DDBA Peptide, UV-DDB1 Peptide, XAP1 Peptide, XPCE Peptide, XPE Peptide, XPE-BF Peptide, DDB1 Peptide, xpe Peptide, ddba Peptide, xap1 Peptide, xpce Peptide, xpe-bf Peptide, uv-ddb1 Peptide, ddb1 Peptide, 127kDa Peptide, AA408517 Peptide, p127-Ddb1 Peptide, damage specific DNA binding protein 1 Peptide, damage-specific DNA binding protein 1, 127kDa Peptide, DNA damage-binding protein 1 Peptide, damage-specific DNA binding protein 1 Peptide, DDB1 Peptide, ddb1 Peptide, LOC100187356 Peptide, Ddb1 Peptide, ddb-1 Peptide
- Background
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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.
Alias Symbols: XPE, DDBA, XAP1, XPCE, XPE-BF, UV-DDB1
Protein Size: 1140 - Gene ID
- 1642
- NCBI Accession
- NM_001923, NP_001914
- UniProt
- Q16531
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