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HEMK1 抗体 (AA 21-120)

HEMK1 适用: 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1714060
发货至: 中国
  • 抗原 See all HEMK1 抗体
    HEMK1 (HemK Methyltransferase Family Member 1 (HEMK1))
    抗原表位
    • 15
    • 8
    • 8
    • 2
    AA 21-120
    适用
    • 36
    • 15
    • 13
    小鼠
    宿主
    • 37
    • 1
    克隆类型
    • 38
    多克隆
    标记
    • 10
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This HEMK1 antibody is un-conjugated
    应用范围
    • 33
    • 19
    • 15
    • 14
    • 3
    • 1
    Western Blotting (WB), ELISA
    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
  • 应用备注
    WB 1:300-5000
    ELISA 1:500-1000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
    4 °C,-20 °C
    储存方法
    Shipped at 4°C. Store at -20°C for one year. 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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