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MAGT1 anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement MAGT1 dans WB et FACS. Il présente une réactivité envers Humain et Souris.
N° du produit ABIN651247

Aperçu rapide pour MAGT1 anticorps (N-Term) (ABIN651247)

Antigène

Voir toutes MAGT1 Anticorps
MAGT1 (Magnesium Transporter 1 (MAGT1))

Reactivité

  • 16
  • 11
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 16
Lapin

Clonalité

  • 16
Polyclonal

Conjugué

  • 10
  • 2
  • 1
  • 1
  • 1
  • 1
Cet anticorp MAGT1 est non-conjugé

Application

  • 16
  • 11
  • 10
  • 2
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Clone

RB25786
  • Épitope

    • 8
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 44-71, N-Term

    Homologie

    C

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This MAGT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 44-71 amino acids from the N-terminal region of human MAGT1.

    Isotype

    IgG
  • Indications d'application

    WB: 1:1000. FC: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Stockage commentaire

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Date de péremption

    6 months
  • Antigène

    MAGT1 (Magnesium Transporter 1 (MAGT1))

    Autre désignation

    MAGT1

    Sujet

    MAGT1 encodes a magnesium cation transporter protein that localizes to the cell membrane. This protein also associates with N-oligosaccharyl transferase and therefore may have a role in N-glycosylation. Mutations in this gene cause mental retardation X-linked type 95 (MRX95). This gene may have multiple in-frame translation initiation sites, one of which would encode a shorter protein with an N-terminus containing a signal peptide at amino acids 1-29.

    Poids moléculaire

    38037

    ID gène

    84061

    NCBI Accession

    NP_115497

    UniProt

    Q9H0U3

    Pathways

    Cell RedoxHomeostasis
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