DDB1 antibody (AA 198-213)
Quick Overview for DDB1 antibody (AA 198-213) (ABIN303090)
Target
See all DDB1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 198-213
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Specificity
- This antibody reacts to amino acids 198-213 of DDB1 (internal) coupled to KLH.
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Cross-Reactivity (Details)
- Species reactivity (tested):Human.
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Purification
- Delipidation and Defibrination.
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Immunogen
- Synthetic peptide (coupled to KLH) corresponding to amino acids 198-213 of Human DDB1 (internal).
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Application Notes
- ELISA: 1/2000-1/10000. Immunoprecipitation. Western Blot: 1/500-1/1000. Immunohistochemistry on Paraffin Sections: 1/500. This antibody was validated for use in immunohistochemistry on a panel of 21formalin-fixed, paraffin-embedded (FFPE) human tissues after heat induced antigenretrieval in pH 6.0 citrate buffer. After incubation with the primary antibody, slides wereincubated with biotinylated secondary antibody LS-D1, followed by alkalinephosphatase-streptavidin and chromogen.
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 85 mg/mL
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Handling Advice
- Avoid repeated freezing and thawing.
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Storage
- 4 °C/-20 °C
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Storage Comment
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.
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- DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))
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Alternative Name
- DDB1 / XAP1
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Background
- DDB1 is also known as damage-specific DNA binding protein 1, DDB p127 subunit, DDBa, UV-damaged DNA-binding protein 1, UV-DDB 1, Xeroderma pigmentosum group E complementing protein, XPCe, X-associated protein 1 and XAP-1. The DDB1 gene encodes the large subunit (p127) of DNA damage-binding protein, which is a heterodimer, composed of a large and a small subunit (p48 DDB2). This nuclear protein functions in nucleotide-excision repair resulting from UV-damaged DNA by binding to pyrimidine dimers. Its defective activity causes the repair defect in the patients with xeroderma pigmentosum complementation group E (XPE). XP-E is a rare human autosomal recessive disease characterized by solar sensitivity, high predisposition for developing cancers on areas exposed to sunlight and, in some cases, neurological abnormalities. 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.Synonyms: DDBa, DNA damage-binding protein 1, DNA damage-binding protein a, Damage-specific DNA-binding protein 1, HBV X-associated protein 1, UV-DDB 1, UV-damaged DNA-binding factor, XAP-1, XPCe, XPE-BF, Xeroderma pigmentosum group E-complementing protein
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Gene ID
- 100290337
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NCBI Accession
- NP_001914
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UniProt
- Q16531
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Pathways
- DNA Damage Repair
Target
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