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ZNF704 抗体 (AA 56-180) (HRP)

This anti-ZNF704 antibody is a 兔 多克隆 antibody detecting ZNF704 in ELISA, IHC (fro) 和 IHC (p). Suitable for 人.
产品编号 ABIN1413884
发货至: 中国

Quick Overview for ZNF704 抗体 (AA 56-180) (HRP) (ABIN1413884)

抗原

ZNF704 (Zinc Finger Protein 704 (ZNF704))

适用

宿主

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克隆类型

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多克隆

标记

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This ZNF704 antibody is conjugated to HRP

应用范围

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

    AA 56-180

    预测反应

    Human,Mouse,Rat,Dog,Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human ZNF704

    亚型

    IgG
  • 应用备注

    IHC-P 1:200-400
    IHC-F 1:100-500

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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.

    注意事项

    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    ZNF704 (Zinc Finger Protein 704 (ZNF704))

    别名

    ZNF704

    背景

    Synonyms: Gig1, Zinc finger protein 704, ZN704_HUMAN, ZNF704.

    Background: Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. The majority of zinc-finger proteins contain a Kr_ppel-type DNA binding domain and a KRAB domain, which is thought to interact with KAP1, thereby recruiting histone modifying proteins. As a member of the krueppel C2H2-type zinc-finger protein family, ZNF704 is a 412 amino acid nuclear protein that contains one C2H2-type zinc finger. The gene encoding ZNF704 maps to human chromosome 8, which is made up of nearly 146 million bases and encodes about 800 genes. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.

    基因ID

    619279
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