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BAZ1B 抗体 (N-Term)

BAZ1B 适用: 人 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN965640
发货至: 中国
  • 抗原 See all BAZ1B 抗体
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    抗原表位
    • 15
    • 9
    • 3
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    • 2
    • 2
    • 1
    • 1
    • 1
    N-Term
    适用
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    • 14
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    宿主
    • 48
    • 5
    克隆类型
    • 41
    • 12
    多克隆
    标记
    • 21
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    • 1
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    This BAZ1B antibody is un-conjugated
    应用范围
    • 22
    • 16
    • 14
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    • 7
    • 5
    • 3
    • 3
    • 3
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    Immunohistochemistry (IHC)
    纯化方法
    Purified by antigen-specific affinity chromatography.
    免疫原
    Polyclonal antibody produced in rabbits immunizing with a synthetic peptide corresponding to N-terminal residues of human BAZ1B (bromodomain adjacent to zinc finger domain, 1B)
    Top Product
    Discover our top product BAZ1B Primary Antibody
  • 应用备注
    ELISA, Western blotting: 1µg/ml for 2hrs.
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    This antibody is stored in PBS, 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
  • Lu, Meng, Morris, Keating: "A novel human gene, WSTF, is deleted in Williams syndrome." in: Genomics, Vol. 54, Issue 2, pp. 241-9, (1999) (PubMed).

  • 抗原
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    别名
    BAZ1B (BAZ1B 产品)
    背景
    The BAZ1B (bromodomain adjacent to zinc finger domain, 1B) is a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing of this gene generates at least 2 transcript variants.
    途径
    Nuclear Hormone Receptor Binding, Chromatin Binding
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