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C22orf9 抗体 (Biotin)

C22orf9 适用: 人, 小鼠, 大鼠 WB, IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1405795
发货至: 中国
  • 抗原 See all C22orf9 products
    C22orf9 (Chromosome 22 Open Reading Frame 9 (C22orf9))
    适用
    • 18
    • 18
    • 18
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 18
    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 C22orf9 antibody is conjugated to Biotin
    应用范围
    • 17
    • 13
    • 2
    • 1
    Western Blotting (WB), 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 C22orf9
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    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
    C22orf9 (Chromosome 22 Open Reading Frame 9 (C22orf9))
    别名
    C22orf9 (C22orf9 产品)
    别名
    c22orf9 antibody, C22orf9 antibody, AW554572 antibody, mKIAA0930 antibody, KIAA0930 S homeolog antibody, KIAA0930 antibody, RIKEN cDNA 5031439G07 gene antibody, similar to CG9646-PA antibody, KIAA0930 ortholog antibody, kiaa0930.S antibody, KIAA0930 antibody, kiaa0930 antibody, 5031439G07Rik antibody, RGD1304694 antibody, Kiaa0930 antibody
    背景

    Synonyms: Chromosome 22 open reading frame 9, Hypothetical protein LOC23313, KIAA0930, Uncharacterized protein C22orf9, K0930_HUMAN.

    Background: C22orf9 is a 404 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.

    基因ID
    23313
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