GFM2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2721847

Détail du produit

Antigène: GFM2 (G Elongation Factor, Mitochondrial 2 (GFM2))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette GFM2 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human GFM2 / EFG2 (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: GFM2 (G Elongation Factor, Mitochondrial 2 (GFM2))

Autre désignation: Gfm2,efg2 (GFM2 Produits)

Synonymes: RGD1309854 Protein, 6530419G12Rik Protein, A930009M04Rik Protein, EF-G2mt Protein, EFG2 Protein, MST027 Protein, RRF2mt Protein, mEF-G 2 Protein, si:dkey-35i22.3 Protein, zgc:153835 Protein, MRRF2 Protein, RRF2 Protein, hEFG2 Protein, ST15 Protein, G elongation factor, mitochondrial 2 Protein, G elongation factor mitochondrial 2 Protein, ribosome-releasing factor 2, mitochondrial Protein, reversion inducing cysteine rich protein with kazal motifs Protein, Gfm2 Protein, GFM2 Protein, gfm2 Protein, LOC662021 Protein, RECK Protein

Sujet: 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, which is a GTPase that plays a role at the termination of mitochondrial translation by mediating the disassembly of ribosomes from messenger RNA. Its role in the regulation of normal mitochondrial function and in disease states attributed to mitochondrial dysfunction is not known. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Poids moléculaire: 86.4 kDa

NCBI Accession: NP_115756

Pathways: Ribonucleoprotein Complex Subunit Organization