SLMAP anticorps (AA 25-607) (Cy3)

N° du produit ABIN8034581

Cet anticorps Lapin Polyclonal détecte spécifiquement SLMAP dans FACS. Il présente une réactivité avec des échantillons de Humain et Souris.

Aperçu rapide pour SLMAP anticorps (AA 25-607) (Cy3) (ABIN8034581)

Antigène: SLMAP (Sarcolemma Associated Protein (SLMAP))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLMAP est conjugé à/à la Cy3

Application: Flow Cytometry (FACS)

Détail du produit anti-SLMAP anticorps (Cy3)

Épitope: AA 25-607

Fonction: Anti-SLMAP Antibody Cy3 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human SLMAP recombinant protein (Position: D25-E607).

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, 1-3 μg/1x10⁶ cells

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 SLMAP

Antigène: SLMAP (Sarcolemma Associated Protein (SLMAP))

Autre désignation: SLMAP

Sujet:

Background: Sarcolemmal membrane-associated protein is a protein that in humans is encoded by the SLMAP gene. This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants.

Gene Full Name: sarcolemma associated protein

ID gène: 7871

UniProt: Q14BN4