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DDB1 抗体 (AA 951-1140)

This anti-DDB1 antibody is a 兔 多克隆 antibody detecting DDB1 in ELISA, IHC (p), IHC (fro), IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN742455
发货至: 中国

Quick Overview for DDB1 抗体 (AA 951-1140) (ABIN742455)

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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ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 8
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    AA 951-1140

    预测反应

    Human,Mouse,Rat,Cow,Horse,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human DDB1

    亚型

    IgG
  • 应用备注

    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    储存条件

    4 °C,-20 °C

    储存方法

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    有效期

    12 months
  • 抗原

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

    别名

    DDB1

    背景

    Synonyms: DNA damage-binding protein 1, DDB1, DDB-1, ,Damage specic DNA binding protein 1, DDB 1, DDB p127 subunit, DDBa, DNA damage binding protein 1, UV damaged DNA binding factor, UV damaged DNA binding protein 1, UV DDB 1, UV-DDB1, X associated protein 1, XAP 1, XAP1, Xeroderma pigmentosum group E complementing protein, XPCE, XPE, XPE binding factor, XPE-BF.

    Background: This gene encodes the large subunit of DNA damage-binding protein which is a heterodimer composed of a large and a small subunit. This protein functions in nucleotide-excision repair. Its defective activity causes the repair defect in the patients with xeroderma pigmentosum complementation group E (XPE). 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. [provided by RefSeq].

    基因ID

    1642

    途径

    DNA Damage Repair
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