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EYA4 抗体 (N-Term)

This anti-EYA4 antibody is a 兔 多克隆 antibody detecting EYA4 in WB. Suitable for 人.
产品编号 ABIN7468333
发货至: 中国

Quick Overview for EYA4 抗体 (N-Term) (ABIN7468333)

抗原

See all EYA4 抗体
EYA4 (Eyes Absent Homolog 4 (EYA4))

适用

  • 40
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1

宿主

  • 39
  • 1

克隆类型

  • 40
多克隆

标记

  • 17
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This EYA4 antibody is un-conjugated

应用范围

  • 18
  • 17
  • 13
  • 13
  • 13
  • 11
  • 7
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 15
    • 9
    • 5
    • 3
    • 3
    • 3
    • 2
    • 1
    N-Term

    交叉反应

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the N-terminus region of human EYA4. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: A431 , HeLa

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.26 mg/mL

    缓冲液

    1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

    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

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    EYA4 (Eyes Absent Homolog 4 (EYA4))

    别名

    EYA transcriptional coactivator and phosphatase 4

    背景

    Synonyms: EYA transcriptional coactivator and phosphatase 4 , CMD1J , DFNA10

    Background: This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may act as a transcriptional activator through its protein phosphatase activity, and it may be important for eye development, and for continued function of the mature organ of Corti. Mutations in this gene are associated with postlingual, progressive, autosomal dominant hearing loss at the deafness, autosomal dominant nonsyndromic sensorineural 10 locus. Defects in this gene are also associated with dilated cardiomyopathy 1J. Three transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq]

    分子量

    70 kDa

    基因ID

    2070

    UniProt

    O95677

    途径

    Sensory Perception of Sound
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