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T-Box 1 抗体 (AA 327-356)

This 兔 多克隆 antibody specifically detects T-Box 1 in WB, IF 和 IHC (p). It exhibits reactivity toward 人.
产品编号 ABIN7873976
发货至: 中国
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Quick Overview for T-Box 1 抗体 (AA 327-356) (ABIN7873976)

抗原

See all T-Box 1 (TBX1) 抗体
T-Box 1 (TBX1)

适用

  • 70
  • 31
  • 29
  • 4
  • 4
  • 2
  • 1

宿主

  • 68
  • 2
  • 1

克隆类型

  • 57
  • 14
多克隆

标记

  • 31
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This T-Box 1 antibody is un-conjugated

应用范围

  • 55
  • 26
  • 26
  • 23
  • 20
  • 15
  • 10
  • 7
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 16
    • 8
    • 8
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 327-356

    原理

    TBX1 Antibody / T-box protein 1

    纯化方法

    Antigen affinity purified

    免疫原

    A portion of amino acids 327-356 from the human protein was used as the immunogen for the TBX1 antibody.

    亚型

    Ig Fraction
  • 应用备注

    The stated application concentrations are suggested starting points. Titration of the TBX1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    In 1X PBS, pH 7.4, with 0.09 % 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

    -20 °C

    储存方法

    Aliquot the TBX1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    T-Box 1 (TBX1)

    别名

    TBX1

    背景

    TBX1 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.

    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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