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C9orf68 抗体 (AA 201-300) (Biotin)

C9orf68 适用: 人 ELISA, IHC (fro), IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1699952
发货至: 中国
  • 抗原 See all C9orf68 products
    C9orf68 (Chromosome 9 Open Reading Frame 68 (C9orf68))
    抗原表位
    • 14
    • 1
    • 1
    • 1
    AA 201-300
    适用
    宿主
    • 16
    • 2
    克隆类型
    • 18
    多克隆
    标记
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C9orf68 antibody is conjugated to Biotin
    应用范围
    • 13
    • 13
    • 4
    • 2
    • 2
    • 2
    • 1
    ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    预测反应
    Human
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C9orf68
    亚型
    IgG
  • 应用备注
    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
    C9orf68 (Chromosome 9 Open Reading Frame 68 (C9orf68))
    别名
    C9orf68 (C9orf68 产品)
    别名
    MGC131199 antibody, MGC146453 antibody, C9orf68 antibody, bA6J24.2 antibody, spermatogenesis associated 6-like L homeolog antibody, spermatogenesis associated 6-like antibody, spermatogenesis associated 6 like antibody, spata6l.L antibody, spata6l antibody, SPATA6L antibody
    背景

    Synonyms: bA6J24.2, chromosome 9 open reading frame 68, FLJ10058, RP11-280I16.2, Uncharacterized protein C9orf68,SPA6L_HUMAN.

    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 C9orf68 gene product has been provisionally designated C9orf68 pending further characterization. There are two isoforms of C9orf68 that are produced as a result of alternative splicing events.

    基因ID
    55064
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