Fibrillin 1 anticorps

N° du produit ABIN2461618

Cet anticorps Lapin Polyclonal détecte spécifiquement Fibrillin 1 dans WB et ELISA. Il présente une réactivité envers Humain et Chien.

Aperçu rapide pour Fibrillin 1 anticorps (ABIN2461618)

Antigène: Fibrillin 1 (FBN1)

Reactivité: Humain, Chien

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Fibrillin 1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Fibrillin 1 anticorps

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FBN1.

Information d'application

Indications d'application: FBN1 antibody can be used for detection of FBN1 by ELISA at 1:1562500. FBN1 antibody can be used for detection of FBN1 by western blot at 0.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store FBN1 antibody at -20 °C.

Détails sur Fibrillin 1

Antigène: Fibrillin 1 (FBN1)

Autre désignation: FBN1

Sujet: FBN1 is a member of the fibrillin family. FBN1 is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated with Marfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.

Poids moléculaire: 21 kDa, 312 kDa

ID gène: 2200

UniProt: Q75N89

Pathways: Maintenance of Protein Location, SARS-CoV-2 Protein Interactome