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T-Box 19 抗体

TBX19 适用: 人, 小鼠 WB, IP, IHC (p), FACS, IF (cc) 宿主: 兔 Monoclonal 1F11 unconjugated
产品编号 ABIN6945138
发货至: 中国
  • 抗原 See all T-Box 19 (TBX19) 抗体
    T-Box 19 (TBX19)
    适用
    • 10
    • 6
    • 6
    • 5
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    人, 小鼠
    宿主
    • 10
    • 1
    克隆类型
    • 10
    • 1
    单克隆
    标记
    • 11
    This T-Box 19 antibody is un-conjugated
    应用范围
    • 11
    • 4
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc))
    交叉反应
    人, 小鼠
    纯化方法
    Purified by Protein A.
    免疫原
    Recombinant protein within human TBXT aa 200-400.
    克隆位点
    1F11
    亚型
    IgG
    Top Product
    Discover our top product TBX19 Primary Antibody
  • 应用备注
    WB 1:300-5000
    FCM 1:20-100
    IHC-P 1:200-400
    IF(ICC) 1:50-200
    IP(1-2 μg)
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 1xTBS ( pH 7.4), 1 % BSA, 40 %Glycerol and 0.05 % Sodium Azide.
    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
    T-Box 19 (TBX19)
    别名
    TBXT (TBX19 产品)
    别名
    TBX19 antibody, TBS19 antibody, TPIT antibody, dJ747L4.1 antibody, CH-TBXT antibody, TBXT antibody, AU019250 antibody, D1Ertd754e antibody, Tpit antibody, T-box 19 antibody, TBX19 antibody, Tbx19 antibody
    背景

    Synonyms: T-box transcription factor T, TBXT, Brachyury protein

    Background: TBXTis an embryonic nuclear transcription factor that binds to a specific DNA element, the palindromic T-site. It binds through a region in its N-terminus, called the T-box, and effects transcription of genes required for mesoderm formation and differentiation. The protein is localized to notochord-derived cells. Variation in this gene was associated with susceptibility to neural tube defects and chordoma. A mutation in this gene was found in a family with sacral agenesis with vertebral anomalies. Involved in the transcriptional regulation of genes required for mesoderm formation and differentiation.

    基因ID
    6862
    UniProt
    O15178
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