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BAZ1B 抗体 (N-Term)

BAZ1B 适用: 人 WB 宿主: 兔 Polyclonal RB40230 unconjugated
产品编号 ABIN1539094
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
    • 8
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 157-186, N-Term
    适用
    • 53
    • 14
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    宿主
    • 48
    • 5
    克隆类型
    • 41
    • 12
    多克隆
    标记
    • 21
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This BAZ1B antibody is un-conjugated
    应用范围
    • 21
    • 16
    • 14
    • 13
    • 7
    • 6
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This BAZ1B antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 157-186 amino acids from the N-terminal region of human BAZ1B.
    克隆位点
    RB40230
    亚型
    Ig Fraction
    Top Product
    Discover our top product BAZ1B Primary Antibody
  • 应用备注
    WB: 1:1000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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
    4 °C,-20 °C
    储存方法
    BAZ1B Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
    有效期
    6 months
  • 抗原
    BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
    别名
    BAZ1B (BAZ1B 产品)
    背景
    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.
    分子量
    170903
    基因ID
    9031
    NCBI登录号
    NP_115784
    UniProt
    Q9UIG0
    途径
    Nuclear Hormone Receptor Binding, Chromatin Binding
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