NK2 Homeobox 5 Protein (NKX2-5) (Myc-DYKDDDDK Tag)

N° du produit ABIN2727353

Détail du produit

Antigène: NK2 Homeobox 5 (NKX2-5)

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette NK2 Homeobox 5 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human NKX2-5 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

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

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

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.

Détail du antigène

Antigène: NK2 Homeobox 5 (NKX2-5)

Autre désignation: Nkx2-5 (NKX2-5 Produits)

Synonymes: CHNG5 Protein, CSX Protein, CSX1 Protein, HLHS2 Protein, NKX2.5 Protein, NKX2E Protein, NKX4-1 Protein, VSD3 Protein, Csx Protein, Nkx-2.5 Protein, Nkx2.5 Protein, tinman Protein, nk2.5 Protein, nkx2-5 Protein, zgc:111912 Protein, AR2 Protein, XNkx2-5 Protein, csx Protein, nkx-2.5 Protein, nkx2-5b Protein, nkx2.5 Protein, NKX2-5 Protein, Nkx2-5 Protein, csx1 Protein, nkx2e Protein, XNkx-2.5 Protein, CNKX-2.5 Protein, NKX-2.5 Protein, NK2 homeobox 5 Protein, NK2 homeobox 5 S homeolog Protein, NKX2-5 Protein, Nkx2-5 Protein, nkx2.5 Protein, nkx2-5.S Protein, nkx2-5 Protein

Sujet: This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.

Poids moléculaire: 34.7 kDa

NCBI Accession: NP_004378

Pathways: Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development