FLNB anticorps (AA 397-701)

N° du produit ABIN7874650

Cet anticorps anti-FLNB Monoclonal Souris (Clone 11E2D2) (ABIN7874650) détecte spécifiquement FLNB dans WB, IF et IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour FLNB anticorps (AA 397-701) (ABIN7874650)

Antigène: FLNB (Filamin B, beta (FLNB))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp FLNB est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: 11E2D2

Détail du produit anti-FLNB anticorps

Épitope: AA 397-701

Fonction: Filamin B Antibody / Migfilin-1 / FLNB / FBLIM1

Purification: Affinity purified

Immunogène: Recombinant human protein (amino acids Q397-D701) was used as the immunogen for the Filamin B antibody.

Isotype: IgG1

Information d'application

Indications d'application: Optimal dilution of the Filamin B antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the Filamin B antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur FLNB

Antigène: FLNB (Filamin B, beta (FLNB))

Autre désignation: Filamin B

Sujet: Filamin B, beta (FLNB), also known as Filamin B (truncated actin binding protein 278 homolog), is a cytoplasmic protein which in humans is encoded by the FLNB gene. This gene encodes a member of the filamin family. The encoded protein interacts with glycoprotein Ib alpha as part of the process to repair vascular injuries. The platelet glycoprotein Ib complex includes glycoprotein Ib alpha, and it binds the actin cytoskeleton. Mutations in this gene have been found in several conditions: atelosteogenesis type 1 and type 3, boomerang dysplasia, autosomal dominant Larsen syndrome, and spondylocarpotarsal synostosis syndrome. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.

UniProt: O75369

Pathways: Maintenance of Protein Location