DDB1 抗体
Quick Overview for DDB1 抗体 (ABIN7467424)
抗原
See all DDB1 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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交叉反应
- 人
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纯化方法
- Protein G purified
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免疫原
- Synthetic peptide congugated to protein carrier. The mice were immunized with a combination of N & C peptide. The Swiss Prot ID is Q16531.
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亚型
- IgG1
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应用备注
- For ELISA: Use at an assay dependent dilution. For WB(ECL): Use at a dilution of 1:1,000 in 5 % Milk/PBS containing 0.05 % Tween. We recommend an overnight incubation at 4!C. Secondary antibody (GTX30590) 2 hours at RT with dilution of 1:5,000 in 5 % Milk/PBS containing 0.05 % Tween. Not tested in other applictions. Optiamal dilutions/concentrations should be determined by the researcher.
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说明
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Positive Control: T47D and MCF-7 whole cell lysate
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 3 mg/mL
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缓冲液
- PBS pH 7.2, No Preservative
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储存液
- Without preservative
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储存条件
- 4 °C,-20 °C
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储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))
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别名
- damage specific DNA binding protein 1
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背景
- Damage specific DNA binding protein 1 , DDBA , UV-DDB1 , XAP1 , XPCE , XPE , XPE-BF,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. [provided by RefSeq, May 2012]
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分子量
- 127 kDa
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基因ID
- 1642
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UniProt
- Q16531
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途径
- DNA Damage Repair
抗原
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