T-Box 1 Protein (TBX1) (Transcript Variant C) (Myc-DYKDDDDK Tag)
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- Target Alle T-Box 1 (TBX1) Proteine anzeigen
- T-Box 1 (TBX1)
- Protein-Typ
- Recombinant
- Proteineigenschaft
- Transcript Variant C
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Spezies
- Human
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Quelle
- HEK-293 Cells
- Aufreinigungstag / Konjugat
- Dieses T-Box 1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
- Applikation
- Antibody Production (AbP), Standard (STD)
- Produktmerkmale
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- Recombinant human TBX1 (transcript variant C) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Reinheit
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product TBX1 Protein
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- Applikationshinweise
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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 - Kommentare
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The tag is located at the C-terminal.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Lagerung
- -80 °C
- Informationen zur Lagerung
- 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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- Target
- T-Box 1 (TBX1)
- Andere Bezeichnung
- Tbx1 (TBX1 Produkte)
- Synonyme
- CAFS Protein, CTHM Protein, DGCR Protein, DGS Protein, DORV Protein, TBX1C Protein, TGA Protein, VCFS Protein, mp:zf637-3-000616 Protein, zgc:136724 Protein, TBX1 Protein, dgs Protein, tga Protein, cafs Protein, cthm Protein, dgcr Protein, dorv Protein, vcfs Protein, tbx1c Protein, xtbx1 Protein, tbx1 Protein, T-box 1 Protein, T-box 1 S homeolog Protein, T-box 1 L homeolog Protein, TBX1 Protein, Tbx1 Protein, tbx1 Protein, tbx1.S Protein, tbx1.L Protein
- Hintergrund
- 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.
- Molekulargewicht
- 52.5 kDa
- NCBI Accession
- NP_542378
- 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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