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PHF6 抗体 (AA 315-349)

PHF6 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5647227
发货至: 中国
  • 抗原 See all PHF6 抗体
    PHF6 (PHD Finger Protein 6 (PHF6))
    抗原表位
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 315-349
    适用
    • 32
    • 6
    • 6
    • 5
    • 5
    • 5
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    宿主
    • 30
    • 2
    克隆类型
    • 31
    • 1
    多克隆
    标记
    • 22
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PHF6 antibody is un-conjugated
    应用范围
    • 20
    • 8
    • 6
    • 5
    • 5
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB)
    交叉反应 (详细)
    Expected species reactivity: Bovine
    纯化方法
    Antigen affinity purified
    免疫原
    A portion of amino acids 315-349 from the human protein was used as the immunogen for the PHF6 antibody.
    亚型
    Ig Fraction
    Top Product
    Discover our top product PHF6 Primary Antibody
  • 应用备注
    Western blot: 1:1000-2000
    限制
    仅限研究用
  • 缓冲液
    In 1X PBS, pH 7.4, with 0.09 % sodium azide
    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
    Aliquot the PHF6 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 抗原
    PHF6 (PHD Finger Protein 6 (PHF6))
    别名
    PHF6 / PHD finger protein 6 (PHF6 产品)
    别名
    zgc:55403 antibody, wu:fa22g03 antibody, BFLS antibody, BORJ antibody, CENP-31 antibody, 2700007B13Rik antibody, 4931428F02Rik antibody, mKIAA1823 antibody, PHD finger protein 6 antibody, PHD finger protein 6 L homeolog antibody, phf6 antibody, phf6.L antibody, PHF6 antibody, Phf6 antibody
    背景
    This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes PHD finger protein 6, a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by mental retardation, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms. [RefSeq]
    基因ID
    84295
    UniProt
    Q8IWS0
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