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T-Box 1 Protein (TBX1) (Transcript Variant A) (Myc-DYKDDDDK Tag)

Recombinant T-Box 1 protein expressed in HEK-293 Cells.
Catalog No. ABIN2733302
$1,112.40
Plus shipping costs $50.00, if applicable $20.00 dry ice
20 μg
Shipping to: United States
Delivery in 11 to 12 Business Days

Quick Overview for T-Box 1 Protein (TBX1) (Transcript Variant A) (Myc-DYKDDDDK Tag) (ABIN2733302)

Target

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

Protein Type

Recombinant

Origin

  • 4
  • 2
  • 1
  • 1
  • 1
Human

Source

  • 3
  • 3
  • 2
  • 1
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Protein Characteristics

    Transcript Variant A

    Purification tag / Conjugate

    This T-Box 1 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human TBX1 (transcript variant A) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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    Product
    Expression System
    Conjugate
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    Expression System HEK-293 Cells
    Conjugate His tag
    Origin Human
    Price starts at $13,686.36
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    Conjugate Strep Tag
    Origin Human
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  • Application Notes

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Comment

    The tag is located at the C-terminal.

    Restrictions

    For Research Use only
  • Concentration

    50 μg/mL

    Buffer

    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

    Storage

    -80 °C

    Storage Comment

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target

    T-Box 1 (TBX1)

    Alternative Name

    Tbx1

    Background

    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.

    Molecular Weight

    43 kDa

    NCBI Accession

    NP_542377

    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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