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FANCC 抗体 (AA 1-558)

This 兔 多克隆 antibody specifically detects FANCC in WB, ELISA 和 FACS. It exhibits reactivity toward 人.
产品编号 ABIN7989639
发货至: 中国
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中国
北京 101111
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Beijing Economic Technological Development Area
Room 801-803
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for FANCC 抗体 (AA 1-558) (ABIN7989639)

抗原

See all FANCC 抗体
FANCC (Fanconi Anemia, Complementation Group C (FANCC))

适用

  • 72
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宿主

  • 67
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克隆类型

  • 68
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多克隆

标记

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This FANCC antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Flow Cytometry (FACS)

质量等级

Carrier-free
  • 抗原表位

    • 17
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    AA 1-558

    原理

    Anti-FANCC Antibody

    交叉反应 (详细)

    No cross-reactivity with other proteins.

    产品特性

    Anti-FANCC Antibody. Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human FANCC recombinant protein (Position: M1-V558).

    亚型

    IgG
  • 应用备注

    Western blot, 0.25-0.5 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human ELISA, 0.1-0.5 μg/mL, -

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    浓度

    500 μg/mL

    缓冲液

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    储存条件

    4 °C,-20 °C

    储存方法

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

    有效期

    12 months
  • 抗原

    FANCC (Fanconi Anemia, Complementation Group C (FANCC))

    别名

    FANCC

    背景

    Background: Fanconi anemia group C protein is a protein that in humans is encoded by the FANCC gene. 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 C.

    Gene Full Name: FA complementation group C

    分子量

    63 kDa

    基因ID

    2176

    UniProt

    Q00597

    途径

    DNA Damage Repair
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