TUFM anticorps

N° du produit ABIN2855161

Cet anticorps Lapin Polyclonal détecte spécifiquement TUFM dans WB, IP et IHC (p). Il présente une réactivité envers 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