PRND anticorps (AA 111-144) (APC)

N° du produit ABIN8025271

Cet anticorps anti-PRND Polyclonal Lapin conjugué à APC (ABIN8025271) détecte spécifiquement PRND dans FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour PRND anticorps (AA 111-144) (APC) (ABIN8025271)

Antigène: PRND (Prion Protein 2 (Dublet) (PRND))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PRND est conjugé à/à la APC

Application: Flow Cytometry (FACS)

Détail du produit anti-PRND anticorps (APC)

Épitope: AA 111-144

Fonction: Anti-PRND Antibody APC Conjugated

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

Homologie: Human PRND shares 69.4% amino acid (aa) sequence identity with mouse PRND.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human PRND recombinant protein (Position: A111-H144). Human PRND shares 69.4% amino acid (aa) sequence identity with mouse PRND.

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 PRND

Antigène: PRND (Prion Protein 2 (Dublet) (PRND))

Autre désignation: PRND

Sujet:

Background: This gene is found on chromosome 20, approximately 20 kbp downstream of the gene encoding cellular prion protein, to which it is biochemically and structurally similar. The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that is found predominantly in testis. Mutations in this gene may lead to neurological disorders.

Gene Full Name: prion like protein doppel

ID gène: 23627

UniProt: Q9UKY0

Pathways: Transition Metal Ion Homeostasis