GFM1 Protein (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes GFM1 Protéines
- GFM1 (G-Elongation Factor, Mitochondrial 1 (GFM1))
- Type de proteíne
- Recombinant
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Origine
- Humain
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Source
- HEK-293 Cells
- Purification/Conjugué
- Cette GFM1 protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human GFM1 / EFG1 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product GFM1 Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- 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.
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- Antigène
- GFM1 (G-Elongation Factor, Mitochondrial 1 (GFM1))
- Autre désignation
- Gfm1,efg1 (GFM1 Produits)
- Synonymes
- 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
- 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. Its role in the regulation of normal mitochondrial function and in different disease states attributed to mitochondrial dysfunction is not known.
- Poids moléculaire
- 83.3 kDa
- NCBI Accession
- NP_079272
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