GFM1 antibody
Contáctenos para saber el precio
Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
935106861
info@markelab.com
name
GFM1 antibody
category
Primary Antibodies
provider
FineTest
reference
FNab03430
tested applications
ELISA, IHC, WB, IF
Description
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.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | G elongation factor, mitochondrial 1 (GFM1) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1:500 - 1:2000; IHC: 1:50 - 1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 100 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, IHC, WB, IF |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.) |
| UniProt ID | Q96RP9 |
| Gene ID | 85476 |
| Alias | Elongation factor G, mitochondrial (EF-Gmt),Elongation factor G 1, mitochondrial (mEF-G 1),Elongation factor G1 (hEFG1),GFM1,EFG,EFG1,GFM |
| Background | Antibody anti-GFM1 |
| Status | RUO |
| Note | Mol. Weight 100 kDa |
Descripción
Related Products
Human GFM1 (Elongation factor G, mitochondrial) ELISA Kit
Ver Producto
Rat GFM1 (Elongation factor G, mitochondrial) ELISA Kit
Ver Producto
GFM1 antibody
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.
Ver Producto