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BAZ1B 抗体

BAZ1B 适用: 人, 小鼠, 大鼠 WB, IHC, IF (cc), IHC (p), IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6989742
发货至: 中国
  • 抗原 See all BAZ1B 抗体
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    适用
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    人, 小鼠, 大鼠
    宿主
    • 53
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    克隆类型
    • 46
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    多克隆
    标记
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    This BAZ1B antibody is un-conjugated
    应用范围
    • 26
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    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human BAZ1B (NP_115784.1).
    亚型
    IgG
    Top Product
    Discover our top product BAZ1B Primary Antibody
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    IF(ICC) 1:50-200
    IHC()
    IF()
    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
    -20 °C
    储存方法
    Store at -20°C for 12 months.
    有效期
    12 months
  • 抗原
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    别名
    BAZ1B (BAZ1B 产品)
    别名
    BAZ1B antibody, wstf antibody, wbscr9 antibody, wbscr10 antibody, LOC100220420 antibody, WBSCR10 antibody, WBSCR9 antibody, WSTF antibody, C87820 antibody, Wbscr9 antibody, fi60d02 antibody, im:7137554 antibody, wu:fi60d02 antibody, bromodomain adjacent to zinc finger domain 1B antibody, bromodomain adjacent to zinc finger domain, 1B antibody, bromodomain adjacent to zinc finger domain 1B S homeolog antibody, BAZ1B antibody, baz1b antibody, Baz1b antibody, baz1b.S antibody
    背景

    Synonyms: BAZ1B,WBSCR10,WBSCR9,WSTF

    Background: This gene encodes 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.

    基因ID
    9031
    UniProt
    Q9UIG0
    途径
    Nuclear Hormone Receptor Binding, Chromatin Binding
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