GTPBP3 anticorps

N° du produit ABIN7466322

Cet anticorps Lapin Polyclonal détecte spécifiquement GTPBP3 dans WB et IHC (p). Il présente une réactivité envers Humain.

Aperçu rapide pour GTPBP3 anticorps (ABIN7466322)

Antigène: GTPBP3 (GTP Binding Protein 3 (Mitochondrial) (GTPBP3))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GTPBP3 est non-conjugé

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

Détail du produit anti-GTPBP3 anticorps

Réactivité croisée: Humain

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human GTPBP3. The exact sequence is proprietary.

Isotype: IgG

Information d'application

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

Commentaires:

Positive Control: IMR32

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 1 % BSA, 20 % 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 GTPBP3

Antigène: GTPBP3 (GTP Binding Protein 3 (Mitochondrial) (GTPBP3))

Autre désignation: GTP binding protein 3, mitochondrial

Sujet: GTP binding protein 3, mitochondrial , COXPD23 , GTPBG3 , MSS1 , MTGP1 , THDF1,This locus encodes a GTP-binding protein. The encoded protein is localized to the mitochondria and may play a role in mitochondrial tRNA modification. Polymorphisms at this locus may be associated with severity of aminoglycoside-induced deafness, a disease associated with a mutation in the 12S rRNA. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq]

Poids moléculaire: 52 kDa

ID gène: 84705

UniProt: Q969Y2