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POMT2 anticorps (C-Term)

Cet anticorps anti-POMT2 est un anticorps Lapin Polyclonal détectant POMT2 dans WB. Adapté pour Humain.
N° du produit ABIN1537449

Aperçu rapide pour POMT2 anticorps (C-Term) (ABIN1537449)

Antigène

Voir toutes POMT2 Anticorps
POMT2 (Protein-O-Mannosyltransferase 2 (POMT2))

Reactivité

  • 21
  • 9
  • 7
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 18
  • 3
Lapin

Clonalité

  • 19
  • 2
Polyclonal

Conjugué

  • 14
  • 2
  • 2
  • 1
  • 1
  • 1
Cet anticorp POMT2 est non-conjugé

Application

  • 19
  • 16
  • 6
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB37546
  • Épitope

    • 7
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 540-567, C-Term

    Homologie

    M

    Purification

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

    Immunogène

    This POMT2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 540-567 amino acids from the C-terminal region of human POMT2.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    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

    POMT2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Date de péremption

    6 months
  • Antigène

    POMT2 (Protein-O-Mannosyltransferase 2 (POMT2))

    Autre désignation

    POMT2

    Sujet

    The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT1 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).

    Poids moléculaire

    84214

    ID gène

    29954

    NCBI Accession

    NP_037514

    UniProt

    Q9UKY4
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