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C16orf72 抗体 (AA 201-275) (FITC)

This anti-C16orf72 antibody is a 兔 多克隆 antibody detecting C16orf72 in WB, IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN1709689
发货至: 中国

Quick Overview for C16orf72 抗体 (AA 201-275) (FITC) (ABIN1709689)

抗原

C16orf72 (Chromosome 16 Open Reading Frame 72 (C16orf72))

适用

  • 20
  • 1

宿主

  • 15
  • 5

克隆类型

  • 15
  • 5
多克隆

标记

  • 7
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This C16orf72 antibody is conjugated to FITC

应用范围

  • 20
  • 12
  • 12
  • 4
  • 4
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    AA 201-275

    预测反应

    Human,Mouse,Rat,Cow,Sheep,Horse,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C16orf72

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    C16orf72 (Chromosome 16 Open Reading Frame 72 (C16orf72))

    别名

    C16orf72

    背景

    Synonyms: C16orf72, Chromosome 16 open reading frame 72, CP072_HUMAN, FLJ41272, Hypothetical protein LOC29035, PRO0149, UPF0472 protein C16orf72.

    Background: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The C16orf72 gene product has been provisionally designated C16orf72 pending further characterization.

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