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DDB1 抗体 (AA 1011-1140)

This anti-DDB1 antibody is a 兔 多克隆 antibody detecting DDB1 in WB, IHC (p), ICC 和 IHC (fro). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN4950780
发货至: 中国

Quick Overview for DDB1 抗体 (AA 1011-1140) (ABIN4950780)

抗原

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

适用

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人, 小鼠, 大鼠

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), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • 抗原表位

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    AA 1011-1140

    纯化方法

    Antigen affinity

    免疫原

    Amino acids 1011-1140 of human DDB1 were used as the immunogen for the DDB1 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the DDB1 antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL,IHC (Paraffin): 0.5-1 μg/mL,IHC (Frozen): 0.5-1 μg/mL,ICC (Paraffin): 0.5-1 μg/mL

    限制

    仅限研究用
  • 缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    -20 °C

    储存方法

    After reconstitution, the DDB1 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • 抗原

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

    别名

    DDB1

    背景

    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. And 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.

    UniProt

    Q16531

    途径

    DNA Damage Repair
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