SEC24D Protein (Myc-DYKDDDDK Tag)

Produktnummer ABIN2731577

Produktdetails

Target: SEC24D (SEC24 Family, Member D (S. Cerevisiae) (SEC24D))

Protein-Typ: Recombinant

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses SEC24D Protein ist gelabelt mit Myc-DYKDDDDK Tag.

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

Produktmerkmale:

• Recombinant human SEC24D 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: SEC24D (SEC24 Family, Member D (S. Cerevisiae) (SEC24D))

Andere Bezeichnung: Sec24d (SEC24D Produkte)

Synonyme: Gm1349 Protein, 2310020L09Rik Protein, sec24d Protein, SEC24 homolog D, COPII coat complex component Protein, Sec24 related gene family, member D (S. cerevisiae) Protein, SEC24 homolog D, COPII coat complex component S homeolog Protein, SEC24D Protein, Sec24d Protein, sec24d.S Protein

Hintergrund: The protein encoded by this gene is a member of the SEC24 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein has similarity to yeast Sec24p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. This gene product is implicated in the shaping of the vesicle, and also in cargo selection and concentration. Mutations in this gene have been associated with Cole-Carpenter syndrome, a disorder affecting bone formation, resulting in craniofacial malformations and bones that break easily. Alternative splicing results in multiple transcript variants encoding different isoforms.

Molekulargewicht: 112.8 kDa

NCBI Accession: NP_055637