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T-Box 1 antibody (C-Term)

This anti-T-Box 1 antibody is a Rabbit Polyclonal antibody detecting T-Box 1 in WB, IHC (p) and EIA. Suitable for Human.
Catalog No. ABIN955110

Quick Overview for T-Box 1 antibody (C-Term) (ABIN955110)

Target

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

Reactivity

  • 53
  • 21
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  • 2
  • 1
Human

Host

  • 51
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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 1
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  • 1
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  • 1
  • 1
  • 1
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  • 1
This T-Box 1 antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
  • Binding Specificity

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    AA 334-364, C-Term

    Specificity

    This antibody reacts to TBX1.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human.

    Purification

    Affinity chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 334~364 amino acids from the C-terminal region of human TBX1

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS, 0.09 % (W/V) sodium azide

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    T-Box 1 (TBX1)

    Alternative Name

    TBX1

    Background

    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.Synonyms: T-box protein 1, T-box transcription factor TBX1, Testis-specific T-box protein

    Molecular Weight

    43133 Da

    Gene ID

    6899

    NCBI Accession

    NP_005983

    Pathways

    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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