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FOXN1 抗体 (C-Term)

This anti-FOXN1 antibody is a 兔 多克隆 antibody detecting FOXN1 in WB. Suitable for 人.
产品编号 ABIN2855969
发货至: 中国
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Quick Overview for FOXN1 抗体 (C-Term) (ABIN2855969)

抗原

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

适用

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宿主

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克隆类型

  • 45
多克隆

标记

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This FOXN1 antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    C-Term

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Rabbit polyclonal antibody to FOXN1 (forkhead box N1)
    FOXN1 antibody [C3], C-term

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human FOXN1. 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: 293T , A431 , HeLa , HepG2 , A549 , H1299 , HCT116 , mouse thymus , rat thymus

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.8 mg/mL

    缓冲液

    1XPBS ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): 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

    FOXN1 (Forkhead Box N1 (FOXN1))

    别名

    forkhead box N1

    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.

    Cellular Localization: Nucleus

    分子量

    69 kDa

    基因ID

    8456

    UniProt

    O15353
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