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IQCJ 抗体 (AA 47-67) (Biotin)

IQCJ 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1400383
发货至: 中国
  • 抗原 See all IQCJ products
    IQCJ (IQ Motif Containing J (IQCJ))
    抗原表位
    • 15
    • 14
    • 8
    • 8
    • 7
    AA 47-67
    适用
    人, 小鼠, 大鼠
    宿主
    • 50
    克隆类型
    • 50
    多克隆
    标记
    • 7
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This IQCJ antibody is conjugated to Biotin
    应用范围
    • 44
    • 26
    • 17
    • 14
    • 13
    • 13
    • 8
    • 3
    • 1
    Western Blotting (WB), ELISA, 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 IQCJ
    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
    IQCJ (IQ Motif Containing J (IQCJ))
    别名
    IQCJ (IQCJ 产品)
    别名
    D230050A05 antibody, EG208426 antibody, IQ motif containing J antibody, IQCJ antibody, Iqcj antibody
    背景

    Synonyms: IQ domain-containing protein J, IQCJ

    Background: IQCJ (IQ domain-containing protein J) is a 159 amino acid protein that contains one IQ domain. Existing as four alternatively spliced isoforms, the gene encoding IQCJ maps to human chromosome 3q25.32. Chromosome 3 houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

    基因ID
    654502
    UniProt
    Q1A5X6
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