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IQCA1 抗体 (Alexa Fluor 594)

IQCA1 适用: 人, 小鼠, 大鼠 WB, IF (p) 宿主: 兔 Polyclonal Alexa Fluor 594
产品编号 ABIN2814891
发货至: 中国
  • 抗原 See all IQCA1 抗体
    IQCA1 (IQ Motif Containing with AAA Domain 1 (IQCA1))
    适用
    人, 小鼠, 大鼠
    宿主
    • 32
    • 1
    克隆类型
    • 32
    多克隆
    标记
    • 10
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This IQCA1 antibody is conjugated to Alexa Fluor 594
    应用范围
    • 32
    • 15
    • 14
    • 12
    • 6
    • 1
    • 1
    • 1
    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 IQCA1
    亚型
    IgG
    Top Product
    Discover our top product IQCA1 Primary Antibody
  • 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
    IQCA1 (IQ Motif Containing with AAA Domain 1 (IQCA1))
    别名
    IQCA1 (IQCA1 产品)
    别名
    4930465P12Rik antibody, 4930585L22Rik antibody, BB288505 antibody, Iqca1 antibody, IQCA antibody, RGD1305311 antibody, IQ motif containing with AAA domain antibody, IQ motif containing with AAA domain 1 antibody, Iqca antibody, IQCA1 antibody, Iqca1 antibody
    背景

    Synonyms: IQ and AAA domain-containing protein 1, IQ mot containing with AAA domain 1, IQCA, Iqca1, IQCA1_HUMAN, RGD1305311, FLJ22527, 4930465P12Rik, FLJ33588.

    Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

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