GFM1 anticorps

N° du produit ABIN5703276

Cet anticorps anti-GFM1 est un anticorps Lapin Polyclonal détectant GFM1 dans WB, IHC, ELISA et IP. Adapté pour Humain, Souris et Rat.

Aperçu rapide pour GFM1 anticorps (ABIN5703276)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GFM1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunoprecipitation (IP)

Détail du produit anti-GFM1 anticorps

Fonction: GFM1 antibody

Immunogène: G elongation factor, mitochondrial 1

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

mouse kidney tissue were subjected to SDS PAGE followed by western blot with FNab03430(GFM1 antibody) at dilution of 1:500

Restrictions: For Research Use only

Stockage

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur GFM1

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

Autre désignation: GFM1

Sujet:

Synonyms: Elongation factor G, mitochondrial (EF-Gmt)|Elongation factor G 1, mitochondrial (mEF-G 1)|Elongation factor G1 (hEFG1)|GFM1|EFG|EFG1|GFM

Background: 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: 70 kDa

ID gène: 85476

UniProt: Q96RP9