TM4SF20 Protein (Myc-DYKDDDDK Tag)

Produktnummer ABIN2733827

Produktdetails

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

Protein-Typ: Recombinant

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses TM4SF20 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

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

Produktmerkmale:

• Recombinant human TM4SF20 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

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

Anwendungsinformationen

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

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: 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.

Antigendetails

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

Andere Bezeichnung: Tm4sf20 (TM4SF20 Produkte)

Synonyme: 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

Hintergrund: 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.

Molekulargewicht: 24.9 kDa

NCBI Accession: NP_079071