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T-Box 5 antibody

The Rabbit Polyclonal anti-T-Box 5 antibody has been validated for WB, ELISA and IHC. It is suitable to detect T-Box 5 in samples from Human and Dog.
Catalog No. ABIN2460713

Quick Overview for T-Box 5 antibody (ABIN2460713)

Target

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

Reactivity

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  • 14
  • 5
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Human, Dog

Host

  • 31
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  • 1
Rabbit

Clonality

  • 32
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Polyclonal

Conjugate

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This T-Box 5 antibody is un-conjugated

Application

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Purification

    Antibody is purified by peptide affinity chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human TBX5.
  • Application Notes

    TBX5 antibody can be used for detection of TBX5 by ELISA at 1:62500. TBX5 antibody can be used for detection of TBX5 by western blot at 0.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Concentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handling Advice

    As with any antibody avoid repeat freeze-thaw cycles.

    Storage

    4 °C/-20 °C

    Storage Comment

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store TBX5 antibody at -20 °C.
  • Target

    T-Box 5 (TBX5)

    Alternative Name

    TBX5

    Background

    TBX5 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.

    Molecular Weight

    39 kDa

    Gene ID

    6910

    NCBI Accession

    NP_542449

    UniProt

    Q99593
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