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TEX33 抗体 (AA 201-280) (AbBy Fluor® 555)

TEX33 适用: 小鼠 IF (p), IF (cc) 宿主: 兔 Polyclonal AbBy Fluor® 555
产品编号 ABIN6978267
发货至: 中国
  • 抗原 See all TEX33 products
    TEX33 (Testis Expressed 33 (TEX33))
    抗原表位
    • 15
    • 14
    • 8
    AA 201-280
    适用
    • 15
    • 14
    小鼠
    宿主
    • 29
    克隆类型
    • 29
    多克隆
    标记
    • 6
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TEX33 antibody is conjugated to AbBy Fluor® 555
    应用范围
    • 15
    • 15
    • 12
    • 12
    • 3
    • 3
    • 1
    • 1
    Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
    交叉反应
    小鼠
    预测反应
    Human,Rat,Dog,Cow,Pig,Horse
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human EAN57
    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
    TEX33 (Testis Expressed 33 (TEX33))
    别名
    EAN57 (TEX33 产品)
    别名
    C22orf33 antibody, EAN57 antibody, cE81G9.2 antibody, 1700061J05Rik antibody, Ean57 antibody, testis expressed 33 antibody, TEX33 antibody, Tex33 antibody
    背景

    Synonyms: C22orf33, cE81G9.2, Chromosome 22 open reading frame 33, Ean57, TEX33_HUMAN, Protein EAN57, Testis expressed sequence 33 protein, TEX33.

    Background: EAN57 is a 59 amino acid protein encoded by the C22orf33 protein. 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.

    基因ID
    339669
    UniProt
    O43247
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