GFM2 anticorps (AA 151-250) (Cy7)

N° du produit ABIN1708690

Cet anticorps Lapin Polyclonal détecte spécifiquement GFM2 dans WB, IF (cc) et IF (p). Il présente une réactivité envers Humain et Rat.

Aperçu rapide pour GFM2 anticorps (AA 151-250) (Cy7) (ABIN1708690)

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

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GFM2 est conjugé à/à la Cy7

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-GFM2 anticorps (Cy7)

Épitope: AA 151-250

Réactivité croisée: Humain, Rat

Homologie: Mouse,Dog,Cow,Sheep,Pig

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human GFM2

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur GFM2

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

Autre désignation: GFM2

Sujet:

Synonyms: EF-G2mt, EFG2, EFG2mt, elongation factor G 2, mitochondrial, Elongation factor G2, G elongation factor mitochondrial 2, GFM2, hEFG2, mEFG 2, mEFG2, Mitochondrial elongation factor G2, mitochondrial ribosome recycling factor 2, MRRF2, MST027, MSTP027, OTTHUMP00000222951, OTTHUMP00000222952, ribosome-releasing factor 2, mitochondrial, RRF2, RRF2mt.

Background: GFM2 is a mitochondrial translation elongation factor. Its role in the regulation of normal mitochondrial function and in different disease states attributed to mitochondrial dysfunction is not known. 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.

ID gène: 84340

UniProt: Q969S9

Pathways: Ribonucleoprotein Complex Subunit Organization