T-Box 5 Protein (TBX5) (Transcript Variant 1) (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes T-Box 5 (TBX5) Protéines
- T-Box 5 (TBX5)
- Type de proteíne
- Recombinant
- Attributs du protein
- Transcript Variant 1
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Origine
- Humain
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Source
- HEK-293 Cells
- Purification/Conjugué
- Cette T-Box 5 protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human TBX5 (transcript variant 1) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product TBX5 Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Stock
- -80 °C
- Stockage commentaire
- 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.
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- Antigène
- T-Box 5 (TBX5)
- Autre désignation
- Tbx5 (TBX5 Produits)
- Synonymes
- TBX5 Protein, tbx-5 Protein, xtbx-5 Protein, xtbx5 Protein, tbx5 Protein, HOS Protein, tbx5.1 Protein, zTbx5 Protein, zf-tbx5 Protein, T-box 5 Protein, T-box 5 L homeolog Protein, T-box 5a Protein, TBX5 Protein, tbx5 Protein, tbx5.L Protein, Tbx5 Protein, tbx5a Protein
- Sujet
- 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.
- Poids moléculaire
- 57.5 kDa
- NCBI Accession
- NP_000183
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