Fibrillin 1 anticorps (C-Term)

N° du produit ABIN2854314

Cet anticorps anti-Fibrillin 1 est un anticorps Lapin Polyclonal détectant Fibrillin 1 dans WB. Adapté pour Humain.

Aperçu rapide pour Fibrillin 1 anticorps (C-Term) (ABIN2854314)

Antigène: Fibrillin 1 (FBN1)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Fibrillin 1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Fibrillin 1 anticorps

Épitope: C-Term

Réactivité croisée: Humain

Attributs du produit: Rabbit Polyclonal antibody to Fibrillin 1 (fibrillin 1)
Fibrillin 1 antibody [C3], C-term

Purification: Affinity purified by Protein A.

Immunogène: Recombinant protein encompassing a sequence within the C-terminus region of human Fibrillin 1. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: HeLa

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 2 mg/mL

Buffer: 1XPBS ( pH 7), 40 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur Fibrillin 1

Antigène: Fibrillin 1 (FBN1)

Autre désignation: fibrillin 1

Sujet: This gene encodes a member of the fibrillin family. The encoded protein 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.

Cellular Localization: Secreted , extracellular space , extracellular matrix

Poids moléculaire: 312 kDa

ID gène: 2200

UniProt: P35555

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