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C22ORF15 抗体 (AA 61-148) (Alexa Fluor 350)

C22ORF15 适用: 人 WB, IF (cc), IF (p) 宿主: 兔 Polyclonal Alexa Fluor 350
产品编号 ABIN1692632
发货至: 中国
  • 抗原 See all C22ORF15 products
    C22ORF15 (Chromosome 22 Open Reading Frame 15 (C22ORF15))
    抗原表位
    AA 61-148
    适用
    宿主
    • 14
    克隆类型
    • 14
    多克隆
    标记
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C22ORF15 antibody is conjugated to Alexa Fluor 350
    应用范围
    • 14
    • 12
    • 12
    • 3
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    预测反应
    Human
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C22orf15
    亚型
    IgG
  • 应用备注
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    C22ORF15 (Chromosome 22 Open Reading Frame 15 (C22ORF15))
    别名
    C22orf15 (C22ORF15 产品)
    别名
    N27C7-3 antibody, chromosome 22 open reading frame 15 antibody, C22orf15 antibody
    背景

    Synonyms: C22orf15, chromosome 22 open reading frame 15, CV015_HUMAN, N27C7 3, Protein N27C7-3, Uncharacterized protein C22orf15.

    Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. 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. The C22orf15 gene product has been provisionally designated C22orf15 pending further characterization.

    基因ID
    150248
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