TUFM anticorps

N° du produit ABIN2855161

Cet anticorps Lapin Polyclonal détecte spécifiquement TUFM dans WB, IP et IHC (p). Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour TUFM anticorps (ABIN2855161)

Antigène: TUFM (Tufm) (Tu Translation Elongation Factor, Mitochondrial (Tufm))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TUFM est non-conjugé

Application: Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-TUFM anticorps

Réactivité croisée: Humain

Attributs du produit: Rabbit Polyclonal antibody to TUFM (Tu translation elongation factor, mitochondrial)
TUFM antibody [N3C3]

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human TUFM. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. IP: 1:100-1:500. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: A431

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 40 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur TUFM

Antigène: TUFM (Tufm) (Tu Translation Elongation Factor, Mitochondrial (Tufm))

Autre désignation: Tu translation elongation factor, mitochondrial

Sujet: This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17.

Poids moléculaire: 50 kDa

ID gène: 7284

UniProt: P49411