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POMT1 anticorps

Cet anticorps anti-POMT1 est un anticorps Lapin Polyclonal détectant POMT1 dans WB. Adapté pour Humain et Souris.
N° du produit ABIN6566852

Aperçu rapide pour POMT1 anticorps (ABIN6566852)

Antigène

Voir toutes POMT1 Anticorps
POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))

Reactivité

  • 45
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 47
Lapin

Clonalité

  • 47
Polyclonal

Conjugué

  • 20
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp POMT1 est non-conjugé

Application

  • 25
  • 15
  • 14
  • 13
  • 13
  • 13
  • 7
  • 4
  • 4
  • 3
  • 1
Western Blotting (WB)
  • Purification

    Affinity purification

    Immunogène

    Recombinant protein of human POMT1

    Isotype

    IgG
  • Indications d'application

    WB 1:1000 - 1:2000

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))

    Autre désignation

    POMT1

    Sujet

    Synonyms: Dolichyl phosphate mannose protein mannosyltransferase 1,Dolichyl phosphate mannose protein mannosyltransferase1,Dolichyl-phosphate-mannose--protein mannosyltransferase 1,LGMD2K,MDDGA1,MDDGB1,MDDGC1,POMT 1,POMT1,POMT1,Protein O mannosyl transferase 1,Protein O mannosyl transferase1,Protein O-mannosyl-transferase 1,Rotate abdomen,Drosophila,homolog of,RT

    Background: The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    Observed_MW: 53kDa

    Calculated_MW: 69kDa/76kDa/82kDa/84kDa

    ID gène

    10585

    UniProt

    Q9Y6A1
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