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ZNF532 抗体 (AA 185-290) (FITC)

This anti-ZNF532 antibody is a 兔 多克隆 antibody detecting ZNF532 in IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN1395968
发货至: 中国
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Quick Overview for ZNF532 抗体 (AA 185-290) (FITC) (ABIN1395968)

抗原

See all ZNF532 抗体
ZNF532 (Zinc Finger Protein 532 (ZNF532))

适用

宿主

  • 15

克隆类型

  • 15
多克隆

标记

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This ZNF532 antibody is conjugated to FITC

应用范围

  • 12
  • 12
  • 3
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Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 1
    AA 185-290

    预测反应

    Human,Mouse,Rat

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human ZNF532

    亚型

    IgG
  • 应用备注

    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

    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.

    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

    ZNF532 (Zinc Finger Protein 532 (ZNF532))

    别名

    ZNF532

    背景

    Synonyms: Zinc finger protein 532, ZN532_HUMAN, Znf532.

    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, ZNF532 is a 1301 amino acid nuclear protein that contains twelve C2H2-type zinc fingers. The gene encoding ZNF532 maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases, representing about 2.5 % of total DNA in cells. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.

    基因ID

    55205
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