GFM1 Protein (Myc-DYKDDDDK Tag)

Produktnummer ABIN2712292

Produktdetails

Target: GFM1 (G-Elongation Factor, Mitochondrial 1 (GFM1))

Protein-Typ: Recombinant

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses GFM1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

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

Produktmerkmale:

• Recombinant human GFM1 / EFG1 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: GFM1 (G-Elongation Factor, Mitochondrial 1 (GFM1))

Andere Bezeichnung: Gfm1,efg1 (GFM1 Produkte)

Synonyme: COXPD1 Protein, EFG Protein, EFG1 Protein, EFGM Protein, EGF1 Protein, GFM Protein, hEFG1 Protein, AW545374 Protein, D3Wsu133e Protein, Gfm Protein, EF-G Protein, Efg Protein, G elongation factor mitochondrial 1 Protein, G elongation factor, mitochondrial 1 Protein, GFM1 Protein, Gfm1 Protein

Hintergrund: Eukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain-oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors. Its role in the regulation of normal mitochondrial function and in different disease states attributed to mitochondrial dysfunction is not known.

Molekulargewicht: 83.3 kDa

NCBI Accession: NP_079272