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DDB1 抗体 (AA 198-213)

The 兔 多克隆 anti-DDB1 antibody (ABIN303090) specifically detects DDB1 in WB, IP, IHC (p) 和 EIA. The antibody is reactive with 人 samples.
产品编号 ABIN303090
发货至: 中国
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Quick Overview for DDB1 抗体 (AA 198-213) (ABIN303090)

抗原

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

适用

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宿主

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克隆类型

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多克隆

标记

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This DDB1 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
  • 抗原表位

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    AA 198-213

    特异性

    This antibody reacts to amino acids 198-213 of DDB1 (internal) coupled to KLH.

    交叉反应 (详细)

    Species reactivity (tested):Human.

    纯化方法

    Delipidation and Defibrination.

    免疫原

    Synthetic peptide (coupled to KLH) corresponding to amino acids 198-213 of Human DDB1 (internal).
  • 应用备注

    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.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    85 mg/mL

    注意事项

    Avoid repeated freezing and thawing.

    储存条件

    4 °C/-20 °C

    储存方法

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.
  • 抗原

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

    别名

    DDB1 / XAP1

    背景

    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

    基因ID

    100290337

    NCBI登录号

    NP_001914

    UniProt

    Q16531

    途径

    DNA Damage Repair
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