SGK196 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2731931

Détail du produit

Antigène: SGK196 (Protein Kinase Protein SgK196 (SGK196))

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette SGK196 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human SGK196 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: SGK196 (Protein Kinase Protein SgK196 (SGK196))

Autre désignation: Sgk196 (SGK196 Produits)

Synonymes: MDDGA12 Protein, SGK196 Protein, Sgk196 Protein, RGD1310810 Protein, sgk196 Protein, wu:fc58e12 Protein, protein-O-mannose kinase Protein, protein-O-mannose kinase L homeolog Protein, POMK Protein, Pomk Protein, pomk Protein, pomk.L Protein

Sujet: This gene encodes a protein that may be involved in the presentation of the laminin-binding O-linked carbohydrate chain of alpha-dystroglycan (a-DG), which forms transmembrane linkages between the extracellular matrix and the exoskeleton. Some pathogens use this O-linked carbohydrate unit for host entry. Loss of function compound heterozygous mutations in this gene were found in a human patient affected by the Walker-Warburg syndrome (WWS) phenotype. Mice lacking this gene contain misplaced neurons (heterotopia) in some regions of the brain, possibly from defects in neuronal migration. Alternative splicing of this gene results in multiple transcript variants.

Poids moléculaire: 39.9 kDa

NCBI Accession: NP_115613