MAGE-Like 2 anticorps (AA 578-847)

N° du produit ABIN8007361

Cet anticorps anti-MAGE-Like 2 Polyclonal Lapin (ABIN8007361) détecte spécifiquement MAGE-Like 2 dans ELISA, IHC, WB et FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour MAGE-Like 2 anticorps (AA 578-847) (ABIN8007361)

Antigène: MAGE-Like 2 (MAGEL2)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MAGE-Like 2 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC), Western Blotting (WB), Flow Cytometry (FACS)

Classe de qualité: Carrier-free

Détail du produit anti-MAGE-Like 2 anticorps

Épitope: AA 578-847

Fonction: Anti-MAGEL2 Antibody

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

Attributs du produit: Anti-MAGEL2 Antibody. Tested in ELISA, IHC, WB, Flow Cytometry applications. This antibody reacts with Human.

Purification: Immunogen affinity purified.

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

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Human Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

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

Poids moléculaire: 133 kDa

ID gène: 54551

UniProt: Q9UJ55