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GPSM2 anticorps

GPSM2 Reactivité: Humain, Souris WB, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7255365
  • Antigène Voir toutes GPSM2 Anticorps
    GPSM2 (G-Protein Signaling Modulator 2 (GPSM2))
    Reactivité
    • 18
    • 13
    • 12
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Humain, Souris
    Hôte
    • 17
    • 1
    Lapin
    Clonalité
    • 18
    Polyclonal
    Conjugué
    • 11
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp GPSM2 est non-conjugé
    Application
    • 8
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human GPSM2 (NP_037428.3).
    Isotype
    IgG
    Top Product
    Discover our top product GPSM2 Anticorps primaire
  • Indications d'application
    WB 1:1000-1:2000 IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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
    GPSM2 (G-Protein Signaling Modulator 2 (GPSM2))
    Autre désignation
    GPSM2 (GPSM2 Produits)
    Sujet
    The protein encoded by this gene belongs to a family of proteins that modulate activation of G proteins, which transduce extracellular signals received by cell surface receptors into integrated cellular responses. The N-terminal half of this protein contains 10 copies of leu-gly-asn (LGN) repeat, and the C-terminal half contains 4 GoLoco motifs, which are involved in guanine nucleotide exchange. This protein may play a role in neuroblast division and in the development of normal hearing. Mutations in this gene are associated with autosomal recessive nonsyndromic deafness (DFNB82). Alternative splicing results in multiple transcript variants.
    Poids moléculaire

    Observed_MW: 76 kDa

    Calculated_MW: 76 kDa

    ID gène
    29899
    UniProt
    P81274
    Pathways
    Regulation of G-Protein Coupled Receptor Protein Signaling
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