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C15orf40 抗体

The 兔 多克隆 anti-C15orf40 antibody (ABIN7246064) specifically detects C15orf40 in ELISA, WB 和 IHC. The antibody is reactive with 人 samples.
产品编号 ABIN7246064
发货至: 中国
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Quick Overview for C15orf40 抗体 (ABIN7246064)

抗原

C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))

适用

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宿主

  • 27
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克隆类型

  • 27
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多克隆

标记

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This C15orf40 antibody is un-conjugated

应用范围

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ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Antigen affinity purification

    免疫原

    Fusion protein of human C15orf40

    亚型

    IgG
  • 应用备注

    WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.5 mg/mL

    缓冲液

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))

    别名

    C15orf40

    背景

    Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The C15orf40 gene product has been provisionally designated C15orf40 pending further characterization.

    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 16 kDa

    UniProt

    Q8WUR7
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