EIF4H anticorps (AA 1-248) (Fluoro488)

N° du produit ABIN7989080

Cet anticorps anti-EIF4H Polyclonal Lapin conjugué à Fluoro488 (ABIN7989080) détecte spécifiquement EIF4H dans FACS. L’anticorps est réactif avec des échantillons de Humain et Singe.

Aperçu rapide pour EIF4H anticorps (AA 1-248) (Fluoro488) (ABIN7989080)

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

Reactivité: Humain, Singe

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp EIF4H est conjugé à/à la Fluoro488

Application: Flow Cytometry (FACS)

Détail du produit anti-EIF4H anticorps (Fluoro488)

Épitope: AA 1-248

Fonction: Anti-EIF4H Antibody Fluoro488 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins

Homologie: Human EIF4Hshares 98.8%,98% amino acid (aa) sequence identity with mouse,rat EIF4H,respectively.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human EIF4H recombinant protein (Position: M1-E248). Human EIF4Hshares 98.8% and 98% amino acid (aa) sequence identity with mouse and rat EIF4H, respectively.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur EIF4H

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

Autre désignation: EIF4H

Sujet:

Background: 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.

Gene Full Name: eukaryotic translation initiation factor 4H

ID gène: 7458

UniProt: Q15056

Pathways: SARS-CoV-2 Protein Interactome