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FOXN1 抗体 (AA 350-378)

The 兔 多克隆 anti-FOXN1 antibody (Clone RB32003) (ABIN655992) specifically detects FOXN1 in WB 和 FACS. The antibody is reactive with 人 samples.
产品编号 ABIN655992
发货至: 中国
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Quick Overview for FOXN1 抗体 (AA 350-378) (ABIN655992)

抗原

See all FOXN1 抗体
FOXN1 (Forkhead Box N1 (FOXN1))

适用

  • 45
  • 21
  • 20
  • 2
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  • 1
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  • 1
  • 1
  • 1

宿主

  • 44
  • 1

克隆类型

  • 45
多克隆

标记

  • 15
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  • 2
  • 1
  • 1
  • 1
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  • 1
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This FOXN1 antibody is un-conjugated

应用范围

  • 34
  • 22
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  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

克隆位点

RB32003
  • 抗原表位

    • 16
    • 6
    • 6
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 350-378

    预测反应

    M

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This FOXN1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 350-378 amino acids from the Central region of human FOXN1.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:2000. FC: 1:10~50

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: 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

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    有效期

    6 months
  • 抗原

    FOXN1 (Forkhead Box N1 (FOXN1))

    别名

    FOXN1

    背景

    Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq].

    分子量

    68925

    基因ID

    8456

    NCBI登录号

    NP_003584

    UniProt

    O15353
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