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T-Box 1 抗体

TBX1 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7254388
发货至: 中国
  • 抗原 See all T-Box 1 (TBX1) 抗体
    T-Box 1 (TBX1)
    适用
    • 53
    • 22
    • 21
    • 4
    • 4
    • 2
    • 1
    宿主
    • 51
    • 2
    • 1
    克隆类型
    • 52
    • 2
    多克隆
    标记
    • 24
    • 5
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This T-Box 1 antibody is un-conjugated
    应用范围
    • 48
    • 24
    • 20
    • 19
    • 14
    • 6
    • 5
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of human TBX1
    亚型
    IgG
    Top Product
    Discover our top product TBX1 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.7 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    T-Box 1 (TBX1)
    别名
    TBX1 (TBX1 产品)
    别名
    CAFS antibody, CTHM antibody, DGCR antibody, DGS antibody, DORV antibody, TBX1C antibody, TGA antibody, VCFS antibody, mp:zf637-3-000616 antibody, zgc:136724 antibody, TBX1 antibody, dgs antibody, tga antibody, cafs antibody, cthm antibody, dgcr antibody, dorv antibody, vcfs antibody, tbx1c antibody, xtbx1 antibody, tbx1 antibody, T-box 1 antibody, T-box 1 S homeolog antibody, T-box 1 L homeolog antibody, TBX1 antibody, Tbx1 antibody, tbx1 antibody, tbx1.S antibody, tbx1.L antibody
    背景
    This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98 % amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.
    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 43 kDa

    UniProt
    O43435
    途径
    Retinoic Acid Receptor Signaling Pathway, Sensory Perception of Sound, Cellular Response to Molecule of Bacterial Origin, Regulation of Muscle Cell Differentiation
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