MAGE-Like 2 anticorps (AA 578-847) (Fluoro647)

N° du produit ABIN8007360

L’anticorps anti-MAGE-Like 2 Polyclonal Lapin est utilisé pour la détection de MAGE-Like 2 dans des échantillons de Humain. Il a été validé pour FACS.

Aperçu rapide pour MAGE-Like 2 anticorps (AA 578-847) (Fluoro647) (ABIN8007360)

Antigène: MAGE-Like 2 (MAGEL2)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MAGE-Like 2 est conjugé à/à la Fluoro647

Application: Flow Cytometry (FACS)

Détail du produit anti-MAGE-Like 2 anticorps (Fluoro647)

Épitope: AA 578-847

Fonction: Anti-MAGEL2 Antibody Fluoro647 Conjugated

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

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human MAGEL2 recombinant protein (Position: Q578-A847).

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 MAGE-Like 2

Antigène: MAGE-Like 2 (MAGEL2)

Autre désignation: MAGEL2

Sujet:

Background: Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS.

Gene Full Name: MAGE family member L2

ID gène: 54551

UniProt: Q9UJ55