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C9orf64 抗体 (AA 161-260) (Biotin)

C9orf64 适用: 人 WB, ELISA, IHC (fro), IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1701204
发货至: 中国
  • 抗原 See all C9orf64 products
    C9orf64 (Chromosome 9 Open Reading Frame 64 (C9orf64))
    抗原表位
    • 14
    • 5
    • 2
    • 2
    • 1
    • 1
    AA 161-260
    适用
    • 25
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 25
    克隆类型
    • 25
    多克隆
    标记
    • 8
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C9orf64 antibody is conjugated to Biotin
    应用范围
    • 21
    • 13
    • 13
    • 6
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    预测反应
    Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C9orf64
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    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
    C9orf64 (Chromosome 9 Open Reading Frame 64 (C9orf64))
    别名
    C9orf64 (C9orf64 产品)
    别名
    C9orf64 antibody, MGC84745 antibody, MGC97544 antibody, chromosome Z C9orf64 homolog antibody, chromosome 9 open reading frame 64 L homeolog antibody, chromosome 9 open reading frame 64 antibody, chromosome 15 open reading frame, human C9orf64 antibody, queuosine salvage protein antibody, CZH9orf64 antibody, c9orf64.L antibody, c9orf64 antibody, C15H9orf64 antibody, C8H9orf64 antibody, C9orf64 antibody
    背景

    Synonyms: C9orf64, CI064_HUMAN, UPF0553 protein C9orf64.

    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 C9orf64 gene product has been provisionally designated C9orf64 pending further characterization.

    基因ID
    84267
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