EIF4H anticorps

N° du produit ABIN7467331

L’anticorps Lapin Polyclonal anti-EIF4H a été validé pour WB, IF et ICC. Il convient pour détecter EIF4H dans des échantillons de Humain.

Aperçu rapide pour EIF4H anticorps (ABIN7467331)

Antigène: EIF4H (Eukaryotic Translation Initiation Factor 4H (EIF4H))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp EIF4H est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC)

Détail du produit anti-EIF4H anticorps

Réactivité croisée: Humain

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human eIF4H. The exact sequence is proprietary.

Isotype: IgG

Information d'application

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

Commentaires:

Positive Control: Raji

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.63 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 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 EIF4H

Antigène: EIF4H (Eukaryotic Translation Initiation Factor 4H (EIF4H))

Autre désignation: eukaryotic translation initiation factor 4H

Sujet: Eukaryotic translation initiation factor 4H , WBSCR1 , WSCR1 , eIF-4H,This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq]

Poids moléculaire: 27 kDa

ID gène: 7458

UniProt: Q15056

Pathways: SARS-CoV-2 Protein Interactome