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FOXN1 抗体 (AA 340-420)

This 兔 多克隆 anti-FOXN1 antibody specifically detects FOXN1 in WB 和 ELISA. The antibody is reactive with 人 samples.
产品编号 ABIN7228580
发货至: 中国
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Quick Overview for FOXN1 抗体 (AA 340-420) (ABIN7228580)

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), ELISA
  • 抗原表位

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    AA 340-420

    原理

    FOXN1 Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of FOXN1 protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human FOXN1 protein at AA range: 340-420

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    -20 °C

    储存方法

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    FOXN1 (Forkhead Box N1 (FOXN1))

    别名

    FOXN1

    背景

    Rabbit Anti-FOXN1 Polyclonal Antibody,Forkhead box protein N1, Winged-helix transcription factor nude,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. FOXN1 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 FOXN1 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.,FOXN1

    分子量

    observerd band 71kDa

    基因ID

    8456

    UniProt

    O15353
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