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T-Box 5 antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects T-Box 5 in WB and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN2798704

Quick Overview for T-Box 5 antibody (N-Term) (ABIN2798704)

Target

See all T-Box 5 (TBX5) Antibodies
T-Box 5 (TBX5)

Reactivity

  • 34
  • 14
  • 6
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
Human

Host

  • 31
  • 3
  • 1
Rabbit

Clonality

  • 32
  • 3
Polyclonal

Conjugate

  • 21
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This T-Box 5 antibody is un-conjugated

Application

  • 28
  • 16
  • 16
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 11
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-30, N-Term

    Purpose

    Rabbit Anti-Human TBX5 (N-term) Antibody

    Immunogen

    This TBX5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human TBX5.

    Isotype

    Ig Fraction
  • Application Notes

    Western Blot, Immunohistochemistry
    Recommended Dilutions
    WB: 1:1000, IHC: 1:10-50TBX5 Antibody (N-term) for immunohistochemistry. Clinical relevance has not been evaluated.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Storage

    4 °C,-20 °C

    Storage Comment

    2-8°C (short-term), -20°C (long-term)
  • Target

    T-Box 5 (TBX5)

    Alternative Name

    TBX5

    Background

    Target Description: 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 is closely linked to related family member T-box 3 (ulnar mammary syndrome) on human chromosome 12. The encoded protein may play a role in heart development and specification of limb identity. Mutations in this gene have been associated with Holt-Oram syndrome, a developmental disorder affecting the heart and upper limbs. Several transcript variants encoding different isoforms have been described for this gene.

    Gene Symbol: TBX5

    Molecular Weight

    57711 Da

    Gene ID

    6910

    UniProt

    Q99593
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