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PHF8 抗体 (AA 501-600) (Biotin)

PHF8 适用: 人 ELISA 宿主: 兔 Polyclonal Biotin
产品编号 ABIN910975
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
    • 1
    • 1
    • 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 Biotin
    应用范围
    • 14
    • 7
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    ELISA
    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
    ELISA 1:500-1000
    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 for 12 months.
    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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