TM4SF20 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2733827

Détail du produit

Antigène: TM4SF20 (Transmembrane 4 L Six Family Member 20 (TM4SF20))

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette TM4SF20 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human TM4SF20 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: TM4SF20 (Transmembrane 4 L Six Family Member 20 (TM4SF20))

Autre désignation: Tm4sf20 (TM4SF20 Produits)

Synonymes: pro994 Protein, tcce518 Protein, PRO994 Protein, TCCE518 Protein, 1810018L02Rik Protein, transmembrane 4 L six family member 20 Protein, transmembrane 4 L six family member 20 L homeolog Protein, TM4SF20 Protein, Tm4sf20 Protein, tm4sf20.L Protein, tm4sf20 Protein

Sujet: The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Knockout of the homologous gene in mouse results in a neurobehavioral phenotype with suggested enhanced motor coordination. A deletion mutation in the human gene is associated with specific language impairment-5.

Poids moléculaire: 24.9 kDa

NCBI Accession: NP_079071