FNBP4 antibody

Catalog No. ABIN7228566

The Rabbit Polyclonal anti-FNBP4 antibody is suitable to detect FNBP4 in samples from Human and Mouse. It has been validated for WB and ELISA.

Quick Overview for FNBP4 antibody (ABIN7228566)

Target: FNBP4 (Formin Binding Protein 4 (FNBP4))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FNBP4 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-FNBP4 Antibody

Purpose: Rabbit Anti-FNBP4 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of FNBP4 protein

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

Immunogen: Synthesized peptide derived from part region of human FNBP4 protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Preservative: ProClin

Precaution of Use: This product contains ProClin: 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 FNBP4

Target: FNBP4 (Formin Binding Protein 4 (FNBP4))

Alternative Name: FNBP4

Background: Formin-binding protein 4, Formin-binding protein 30FNBP4 encodes a protein containing two tryptophan-rich WW domains that binds the proline-rich formin homology 1 domains of formin family proteins, suggesting a role in the regulation of cytoskeletal dynamics during cell division and migration. It also binds intersectin family proteins suggesting a role in the maintenance of membrane curvature at sites of nascent vesicle formation. Naturally occurring mutations in this gene are associated with Waardenburg anophthalmia syndrome. FNBP4 (Formin Binding Protein 4) is a Protein Coding gene. Diseases associated with FNBP4 include Microphthalmia With Limb Anomalies.

Molecular Weight: 111kD

Gene ID: 23360

UniProt: Q8N3X1