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IQCJ 抗体 (AA 47-67) (AbBy Fluor® 680)

This anti-IQCJ antibody is a 兔 多克隆 antibody detecting IQCJ in WB 和 IF (p). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN5005523
发货至: 中国
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Quick Overview for IQCJ 抗体 (AA 47-67) (AbBy Fluor® 680) (ABIN5005523)

抗原

IQCJ (IQ Motif Containing J (IQCJ))

适用

人, 小鼠, 大鼠

宿主

  • 45

克隆类型

  • 45
多克隆

标记

  • 7
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This IQCJ antibody is conjugated to AbBy Fluor® 680

应用范围

  • 39
  • 25
  • 13
  • 13
  • 10
  • 9
  • 8
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 15
    • 14
    • 8
    • 3
    • 2
    AA 47-67

    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

    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

    IQCJ (IQ Motif Containing J (IQCJ))

    别名

    IQCJ

    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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