Formin 2 anticorps (AA 1510-1590)

N° du produit ABIN7223674

Cet anticorps Lapin Polyclonal détecte spécifiquement Formin 2 dans ELISA, IHC et IF. Il présente une réactivité avec des échantillons de Humain et Souris.

Aperçu rapide pour Formin 2 anticorps (AA 1510-1590) (ABIN7223674)

Antigène: Formin 2 (FMN2)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Formin 2 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)

Détail du produit anti-Formin 2 anticorps

Épitope: AA 1510-1590

Fonction: Rabbit Anti-Formin 2 Polyclonal Antibody

Specificité: Formin 2 Polyclonal Antibody detects endogenous levels of Formin 2 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from the C-terminal region of human Formin 2 at AA range: 1510-1590

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC 1:100-1:300,ELISA 1:40000,IF 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur Formin 2

Antigène: Formin 2 (FMN2)

Autre désignation: Formin 2

Sujet: FMN2, Formin-2FMN2 (formin 2) is a member of the formin homology protein family. The encoded protein is thought to have essential roles in organization of the actin cytoskeleton and in cell polarity. Mutations in FMN2 have been associated with mental retardation autosomal recessive 47 (MRT47). Alternatively spliced transcript variants have been identified.

ID gène: 56776

UniProt: Q9NZ56

Pathways: Regulation of Actin Filament Polymerization