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FAM164A 抗体

This anti-FAM164A antibody is a 兔 多克隆 antibody detecting FAM164A in WB, IF (p) 和 IHC (p). Suitable for 人, 大鼠 和 小鼠.
产品编号 ABIN1387566
发货至: 中国

Quick Overview for FAM164A 抗体 (ABIN1387566)

抗原

FAM164A (Family with Sequence Similarity 164, Member A (FAM164A))

适用

  • 41
  • 17
  • 15
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
人, 大鼠, 小鼠

宿主

  • 37
  • 4

克隆类型

  • 40
  • 1
多克隆

标记

  • 16
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FAM164A antibody is un-conjugated

应用范围

  • 35
  • 12
  • 8
  • 6
  • 4
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C8orf70

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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

    4 °C,-20 °C

    储存方法

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    有效期

    12 months
  • 抗原

    FAM164A (Family with Sequence Similarity 164, Member A (FAM164A))

    别名

    CGI62/C8orf70

    背景

    Synonyms: C8orf70, Chromosome 8 open reading frame 70, F164A_HUMAN, fam164a, family with sequence similarity 164, member A, Hypothetical protein C8orf70, hypothetical protein LOC51101, Protein FAM164A, CGI 62, CGI-62.

    Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf70 gene product has been provisionally designated C8orf70 pending further characterization.

    基因ID

    4879
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