Formin 2 antibody (AA 1510-1590)

Catalog No. ABIN7223674

This Rabbit Polyclonal antibody specifically detects Formin 2 in ELISA, IHC and IF. It exhibits reactivity toward Human and Mouse.

Quick Overview for Formin 2 antibody (AA 1510-1590) (ABIN7223674)

Target: Formin 2 (FMN2)

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Formin 2 antibody is un-conjugated

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

Product Details anti-Formin 2 Antibody

Binding Specificity: AA 1510-1590

Purpose: Rabbit Anti-Formin 2 Polyclonal Antibody

Specificity: 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.

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

Isotype: IgG

Application Details

Application Notes: 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

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: 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.

Expiry Date: 12 months

Target Details for Formin 2

Target: Formin 2 (FMN2)

Alternative Name: Formin 2

Background: 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.

Gene ID: 56776

UniProt: Q9NZ56

Pathways: Regulation of Actin Filament Polymerization