Lamin B Receptor anticorps (AA 102-209) (PE)

N° du produit ABIN8005003

Cet anticorps anti-Lamin B Receptor Polyclonal Lapin conjugué à PE (ABIN8005003) détecte spécifiquement Lamin B Receptor dans FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour Lamin B Receptor anticorps (AA 102-209) (PE) (ABIN8005003)

Antigène: Lamin B Receptor (LBR)

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Lamin B Receptor est conjugé à/à la PE

Application: Flow Cytometry (FACS)

Détail du produit anti-Lamin B Receptor anticorps (PE)

Épitope: AA 102-209

Fonction: Anti-Lamin B Receptor/LBR Antibody PE Conjugated

Specificité: No cross reactivity with other proteins.

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

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human Lamin B Receptor/LBR recombinant protein (Position: H102-F209).

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 Lamin B Receptor

Antigène: Lamin B Receptor (LBR)

Autre désignation: LBR

Sujet:

Background: Lamin-B receptor is a protein, and in humans, it is encoded by the LBR gene. It is mapped to 1q42.12. The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified.

Gene Full Name: lamin B receptor

ID gène: 3930

UniProt: Q14739