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HEMK1 抗体 (FITC)

HEMK1 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal FITC
产品编号 ABIN1709762
发货至: 中国
  • 抗原 See all HEMK1 抗体
    HEMK1 (HemK Methyltransferase Family Member 1 (HEMK1))
    适用
    人, 小鼠, 大鼠
    宿主
    • 37
    • 1
    克隆类型
    • 38
    多克隆
    标记
    • 11
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This HEMK1 antibody is conjugated to FITC
    应用范围
    • 33
    • 20
    • 15
    • 14
    • 3
    • 1
    Western Blotting (WB)
    交叉反应
    小鼠
    预测反应
    Human,Rat,Dog,Cow,Horse,Chicken,Rabbit
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human HEMK1
    亚型
    IgG
    Top Product
    Discover our top product HEMK1 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
    Sodium azide
    注意事项
    This product contains Sodium azide: 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
    HEMK1 (HemK Methyltransferase Family Member 1 (HEMK1))
    别名
    Hemk1 (HEMK1 产品)
    别名
    HEMK antibody, MTQ1 antibody, 2310008M14Rik antibody, AW049265 antibody, RGD1308293 antibody, HemK methyltransferase family member 1 antibody, CpipJ_CPIJ016651 antibody, HEMK1 antibody, Hemk1 antibody
    背景

    Synonyms: HEMK, HemK methyltransferase family member 1, Hemk1, HEMK1_HUMAN, M.HsaHemKP, MTQ1.

    Background: HEMK1 is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and 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. name change

    基因ID
    51409
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