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FANCA 抗体 (AA 667-694)

This anti-FANCA antibody is a 兔 多克隆 antibody detecting FANCA in WB. Suitable for 人.
产品编号 ABIN1538566
发货至: 中国

Quick Overview for FANCA 抗体 (AA 667-694) (ABIN1538566)

抗原

See all FANCA 抗体
FANCA (Fanconi Anemia Group A Protein (FANCA))

适用

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宿主

  • 61
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克隆类型

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多克隆

标记

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This FANCA antibody is un-conjugated

应用范围

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Western Blotting (WB)

克隆位点

RB23899
  • 抗原表位

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    AA 667-694

    纯化方法

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

    免疫原

    This FANCA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 667-694 amino acids from the Central region of human FANCA.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000

    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

    FANCA Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    有效期

    6 months
  • 抗原

    FANCA (Fanconi Anemia Group A Protein (FANCA))

    别名

    FANCA

    背景

    The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity, they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia.

    分子量

    162775

    基因ID

    2175

    NCBI登录号

    NP_000126, NP_001018122

    UniProt

    O15360

    途径

    DNA Damage Repair
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