Tricellulin anticorps (AA 12-496) (Fluoro647)

N° du produit ABIN8049492

L’anticorps anti-Tricellulin Polyclonal Lapin est utilisé pour la détection de Tricellulin dans des échantillons de Humain et Rat. Il a été validé pour FACS.

Aperçu rapide pour Tricellulin anticorps (AA 12-496) (Fluoro647) (ABIN8049492)

Antigène: Tricellulin (MARVELD2)

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Tricellulin est conjugé à/à la Fluoro647

Application: Flow Cytometry (FACS)

Détail du produit anti-Tricellulin anticorps (Fluoro647)

Épitope: AA 12-496

Fonction: Anti-MARVELD2 Antibody Fluoro647 Conjugated

Homologie: Human MARVELD2 shares 87% amino acid (aa) sequence identity with mouse MARVELD2.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human MARVELD2 recombinant protein (Position: R12-H496). Human MARVELD2 shares 87% amino acid (aa) sequence identity with mouse MARVELD2.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur Tricellulin

Antigène: Tricellulin (MARVELD2)

Autre désignation: MARVELD2

Sujet:

Background: MARVEL domain-containing protein 2 is a protein that in humans is encoded by the MARVELD2 gene. The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene.

Gene Full Name: MARVEL domain containing 2

ID gène: 153562

UniProt: Q8N4S9

Pathways: Sensory Perception of Sound, Cell-Cell Junction Organization