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BCL7B 抗体 (Biotin)

BCL7B 适用: 人, 小鼠, 大鼠 WB, IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1401913
发货至: 中国
  • 抗原 See all BCL7B 抗体
    BCL7B (B-Cell CLL/lymphoma 7B (BCL7B))
    适用
    人, 小鼠, 大鼠
    宿主
    • 38
    • 3
    克隆类型
    • 39
    • 2
    多克隆
    标记
    • 12
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    This BCL7B antibody is conjugated to Biotin
    应用范围
    • 34
    • 17
    • 15
    • 13
    • 4
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human BCL7B
    亚型
    IgG
    Top Product
    Discover our top product BCL7B Primary Antibody
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    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
    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
    BCL7B (B-Cell CLL/lymphoma 7B (BCL7B))
    别名
    BCL7B (BCL7B 产品)
    别名
    bcl7b antibody, zgc:103501 antibody, wu:fb94h01 antibody, zgc:85678 antibody, B-cell CLL/lymphoma 7B, b antibody, B-cell CLL/lymphoma 7B, a antibody, B-cell CLL/lymphoma 7B antibody, B-cell CLL/lymphoma 7b antibody, B cell CLL/lymphoma 7B antibody, BCL tumor suppressor 7B antibody, bcl7bb antibody, bcl7ba antibody, bcl7b antibody, Bcl7b antibody, BCL7B antibody
    背景

    Synonyms: B cell CLL/lymphoma 7 protein family member B, B cell CLL/lymphoma 7B, BCL 7B, BCL7B_HUMAN.

    Background: BCL7B shows high homology to the BCL7A protein, which is known to be directly involved in a complex chromosomal translocation in Burkitt lymphoma cell lines. The specific function of BCL7B has not yet been determined. However, it may play a role in lung tumor development or progression. The BCL7B gene is located at a chromosomal region commonly deleted in the congenital disorder, Williams syndrome.

    基因ID
    9275
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