Fukutin Protein (FKTN) (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2721450

Détail du produit

Antigène: Fukutin (FKTN)

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

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

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

Attributs du produit:

• Recombinant human Fukutin (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

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: Fukutin (FKTN)

Autre désignation: Fukutin (FKTN Produits)

Synonymes: FCMD Protein, fcmd Protein, im:7163166 Protein, zgc:162828 Protein, FKTN Protein, CMD1X Protein, LGMD2M Protein, MDDGA4 Protein, MDDGB4 Protein, MDDGC4 Protein, D830030O17Rik Protein, Fcmd Protein, fukutin Protein, fukutin S homeolog Protein, Fukutin Protein, FKTN Protein, fktn Protein, fktn.S Protein, Bm1_09375 Protein, Bm1_09380 Protein, Bm1_44655 Protein, Fktn Protein

Sujet: The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene.

Poids moléculaire: 53.5 kDa

NCBI Accession: NP_001073270

Pathways: Regulation of Carbohydrate Metabolic Process