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PGAP1 anticorps (AA 166-904)

L’anticorps anti-PGAP1 Polyclonal Lapin est utilisé pour la détection de PGAP1 dans des échantillons de Humain. Il a été validé pour WB, ELISA et FACS.
N° du produit ABIN7871160
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour PGAP1 anticorps (AA 166-904) (ABIN7871160)

Antigène

Voir toutes PGAP1 Anticorps
PGAP1 (Post-GPI Attachment To Proteins 1 (PGAP1))

Reactivité

  • 9
  • 5
  • 4
  • 2
Humain

Hôte

  • 6
  • 3
Lapin

Clonalité

  • 7
  • 2
Polyclonal

Conjugué

  • 9
Cet anticorp PGAP1 est non-conjugé

Application

  • 7
  • 7
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Épitope

    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 166-904

    Fonction

    PGAP1 Antibody

    Purification

    Antigen affinity chromatography

    Immunogène

    An E.coli-derived human recombinant protein (amino acids K166-R904) was used as the immunogen for the PGAP1 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the PGAP1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the PGAP1 Antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    PGAP1 (Post-GPI Attachment To Proteins 1 (PGAP1))

    Autre désignation

    PGAP1

    Sujet

    Post-GPI attachment to proteins 1 is a protein that in humans is encoded by the PGAP1 gene. The protein encoded by this gene functions early in the glycosylphosphatidylinositol (GPI) biosynthetic pathway, catalyzing the inositol deacylation of GPI. The encoded protein is required for the production of GPI that can attach to proteins, and this may be an important factor in the transport of GPI-anchored proteins from the endoplasmic reticulum to the Golgi. Defects in this gene are a cause an autosomal recessive form of cognitive impairment.

    UniProt

    Q75T13

    Pathways

    Sensory Perception of Sound, Inositol Metabolic Process
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