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C9ORF173 抗体 (AA 201-300) (Biotin)

C9ORF173 适用: 小鼠 WB, ELISA 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1700926
发货至: 中国
  • 抗原 See all C9ORF173 products
    C9ORF173 (Chromosome 9 Open Reading Frame 173 (C9ORF173))
    抗原表位
    • 2
    • 1
    • 1
    AA 201-300
    适用
    • 14
    • 14
    • 12
    小鼠
    宿主
    • 16
    克隆类型
    • 16
    多克隆
    标记
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C9ORF173 antibody is conjugated to Biotin
    应用范围
    Western Blotting (WB), ELISA
    交叉反应
    小鼠
    预测反应
    Human,Rat,Dog
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C9orf173
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    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 for 12 months.
    有效期
    12 months
  • 抗原
    C9ORF173 (Chromosome 9 Open Reading Frame 173 (C9ORF173))
    别名
    C9orf173 (C9ORF173 产品)
    别名
    sperm-tail PG-rich repeat containing 3 antibody, STPG3 antibody
    背景

    Synonyms: C9orf173, Chromosome 9 open reading frame 173, CI173_HUMAN, Uncharacterized protein C9orf173.

    Background: C9orf173 (chromosome 9 open reading frame 173) is a 389 amino acid protein that exists as four alternatively spliced isoforms. The gene encoding C9orf173 maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought 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.

    基因ID
    441476
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