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ATOH7 抗体 (AA 31-120) (AbBy Fluor® 680)

This anti-ATOH7 antibody is a 兔 多克隆 antibody detecting ATOH7 in WB, IF (cc) 和 IF (p). Suitable for 小鼠.
产品编号 ABIN6981057
发货至: 中国

Quick Overview for ATOH7 抗体 (AA 31-120) (AbBy Fluor® 680) (ABIN6981057)

抗原

See all ATOH7 抗体
ATOH7 (Atonal Homolog 7 (ATOH7))

适用

  • 16
  • 16
  • 1
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小鼠

宿主

  • 30
  • 2
  • 1

克隆类型

  • 32
  • 1
多克隆

标记

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  • 1
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This ATOH7 antibody is conjugated to AbBy Fluor® 680

应用范围

  • 29
  • 13
  • 12
  • 12
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 7
    • 3
    • 2
    • 2
    • 2
    • 1
    AA 31-120

    交叉反应

    小鼠

    预测反应

    Human,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human MAT2A

    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

    ATOH7 (Atonal Homolog 7 (ATOH7))

    别名

    MATH5

    背景

    Synonyms: ATOH7, ATOH7_HUMAN, Atonal homolog 7 (Drosophila), Atonal Homolog 7, bHLHa13, Class A basic helix-loop-helix protein 13, hATH5, Helix-loop-helix protein hATH-5, Math5, Protein atonal homolog 7.

    Background: This intronless gene encodes a member of the basic helix-loop-helix family of transcription factors, with similarity to Drosophila atonal gene that controls photoreceptor development. Studies in mice suggest that this gene plays a central role in retinal ganglion cell and optic nerve formation. Mutations in this gene are associated with nonsyndromic congenital retinal nonattachment. [provided by RefSeq, Dec 2011]

    基因ID

    220202

    UniProt

    Q8N100
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