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LARGE anticorps (AA 35-142) (PE)

L’anticorps Souris Monoclonal anti-LARGE a été validé pour FACS. Il convient pour détecter LARGE dans des échantillons de Humain.
N° du produit ABIN5541531

Aperçu rapide pour LARGE anticorps (AA 35-142) (PE) (ABIN5541531)

Antigène

Voir toutes LARGE Anticorps
LARGE (Like-Glycosyltransferase (LARGE))

Reactivité

  • 9
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Humain

Hôte

  • 6
  • 2
  • 1
Souris

Clonalité

  • 8
  • 1
Monoclonal

Conjugué

  • 9
Cet anticorp LARGE est conjugé à/à la PE

Application

  • 8
  • 3
  • 2
  • 1
  • 1
  • 1
Flow Cytometry (FACS)

Clone

LARGE-02
  • Épitope

    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 35-142

    Specificité

    Thisa ntibody recognizes human LARGE1, a glycosyltransferase localizing mainly to the Golgi apparatus. Crossreactivity with LARGE2 was not determined.

    Immunogène

    Recombinant fragment of human LARGE1 (amino acids 35-142)

    Isotype

    IgG2b
  • Indications d'application

    Flow cytometry.

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

    Stockage commentaire

    Store the antibody at 2-8°C. DO NOT FREEZE! This product is photosensitive and should be protected from light. Shelf life: one year from despatch.

    Date de péremption

    12 months
  • Antigène

    LARGE (Like-Glycosyltransferase (LARGE))

    Autre désignation

    large

    Sujet

    LARGE1 serves as a glycosyltransferase which participates in glycosylation of the muscle membrane protein alpha-dystroglycan. Mutations of LARGE1 lead to hypoglycosylation of alpha-dystroglycan and cause congenital muscular dystrophy (MDC1D) associated with severe mental retardation. Altered alpha-dystroglycan glycosylation may also play a role in cancer, as hypoglycosylation of the protein and loss of laminin binding have been demonstrated in invasive carcinoma cells.

    UniProt

    O95461
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