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FAM78A 抗体

FAM78A 适用: 人, 小鼠, 大鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1385951
发货至: 中国
  • 抗原 See all FAM78A products
    FAM78A (Family with Sequence Similarity 78, Member A (FAM78A))
    适用
    • 24
    • 19
    • 19
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    人, 小鼠, 大鼠
    宿主
    • 24
    克隆类型
    • 24
    多克隆
    标记
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FAM78A antibody is un-conjugated
    应用范围
    • 20
    • 12
    • 5
    • 2
    • 2
    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 FAM78A/C9orf59
    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
    FAM78A (Family with Sequence Similarity 78, Member A (FAM78A))
    别名
    C9orf59 (FAM78A 产品)
    别名
    fam78a antibody, zgc:175187 antibody, C9orf59 antibody, A130092J06Rik antibody, RGD1566351 antibody, family with sequence similarity 78 member A antibody, family with sequence similarity 78, member Ab antibody, family with sequence similarity 78, member A antibody, FAM78A antibody, fam78ab antibody, fam78a antibody, Fam78a antibody
    背景

    Synonyms: C9orf59, Chromosome 9 open reading frame 59, Family with sequence similarity 78, member A, FLJ00024, Hypothetical protein LOC286336,FAM78A.

    Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The FAM78A gene product has been provisionally designated FAM78A pending further characterization.

    基因ID
    286336
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