SOX10 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2732430

Détail du produit

Antigène: SOX10 (SRY (Sex Determining Region Y)-Box 10 (SOX10))

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette SOX10 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human SOX10 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: SOX10 (SRY (Sex Determining Region Y)-Box 10 (SOX10))

Autre désignation: Sox10 (SOX10 Produits)

Synonymes: DOM Protein, PCWH Protein, WS2E Protein, WS4 Protein, WS4C Protein, SOX-10 Protein, SOX10 Protein, dom Protein, ws4 Protein, Dom Protein, Sox21 Protein, SOX9 Protein, cls/sox10 Protein, zgc:100757 Protein, SRY-box 10 Protein, SRY box 10 Protein, SRY-box 10 L homeolog Protein, SRY (sex determining region Y)-box 10 Protein, SOX10 Protein, Sox10 Protein, sox10.L Protein, sox10 Protein

Sujet: This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein acts as a nucleocytoplasmic shuttle protein and is important for neural crest and peripheral nervous system development. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease.

Poids moléculaire: 49.7 kDa

NCBI Accession: NP_008872

Pathways: Chromatin Binding