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IQCE 抗体 (FITC)

IQCE 适用: 人, 小鼠, 大鼠 WB, IF (p) 宿主: 兔 Polyclonal FITC
产品编号 ABIN1400366
发货至: 中国
  • 抗原 See all IQCE products
    IQCE (IQ Motif Containing E (IQCE))
    适用
    • 19
    • 17
    • 17
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 19
    克隆类型
    • 18
    多克隆
    标记
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This IQCE antibody is conjugated to FITC
    应用范围
    • 19
    • 12
    • 3
    • 3
    • 2
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (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 IQCE
    亚型
    IgG
  • 应用备注
    IF(IHC-P) 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
    IQCE (IQ Motif Containing E (IQCE))
    别名
    IQCE (IQCE 产品)
    别名
    1700028P05Rik antibody, mKIAA1023 antibody, RGD1311349 antibody, IQ motif containing E antibody, IQCE antibody, Iqce antibody
    背景

    Synonyms: IQ domain-containing protein E, IQ mot containing E, IQCE, IQCE_HUMAN.

    Background: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

    基因ID
    23288
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