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PHF8 抗体 (AA 501-600) (Cy5.5)

PHF8 适用: 人 FACS 宿主: 兔 Polyclonal Cy5.5
产品编号 ABIN910966
发货至: 中国
  • 抗原 See all PHF8 抗体
    PHF8 (PHD Finger Protein 8 (PHF8))
    抗原表位
    • 15
    • 3
    • 2
    • 1
    AA 501-600
    适用
    • 29
    • 11
    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 29
    • 1
    克隆类型
    • 28
    • 2
    多克隆
    标记
    • 9
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PHF8 antibody is conjugated to Cy5.5
    应用范围
    • 13
    • 7
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Flow Cytometry (FACS)
    交叉反应
    预测反应
    Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human PHF8
    亚型
    IgG
    Top Product
    Discover our top product PHF8 Primary Antibody
  • 应用备注
    FCM 1:20-100
    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
    PHF8 (PHD Finger Protein 8 (PHF8))
    别名
    PHF8 (PHF8 产品)
    别名
    9830141C09Rik antibody, mKIAA1111 antibody, JHDM1F antibody, MRXSSD antibody, ZNF422 antibody, RGD1561065 antibody, zPHF8 antibody, PHD finger protein 8 antibody, Phf8 antibody, PHF8 antibody, phf8 antibody
    背景

    Synonyms: PHD finger protein 8, PHD finger protein 8, Histone lysine demethylase PHF8, PHD finger protein 8, PHF8, PHF8_HUMAN, ZNF422.

    Background: The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe(2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. Defects in this gene are a cause of mental retardation syndromic X-linked Siderius type (MRXSSD). Four transcript variants encoding different isoforms have been found for this gene.

    基因ID
    23133
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