Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

FGD1 anticorps (AA 50-100)

FGD1 Reactivité: Humain IP Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7451132
  • Antigène Voir toutes FGD1 Anticorps
    FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))
    Épitope
    • 3
    • 2
    • 1
    AA 50-100
    Reactivité
    • 7
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Humain
    Hôte
    • 7
    Lapin
    Clonalité
    • 7
    Polyclonal
    Conjugué
    • 7
    Cet anticorp FGD1 est non-conjugé
    Application
    • 7
    • 2
    • 1
    • 1
    • 1
    Immunoprecipitation (IP)
    Fonction
    Rabbit anti-FGD1 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogène
    Between AA 50 and 100
    Isotype
    IgG
    Top Product
    Discover our top product FGD1 Anticorps primaire
  • Indications d'application

    IP: 2 - 10 μg/mg lysate

    WB: Not recommended. ABIN7451132 has not performed satisfactorily when used for WB of FGD1 in crude preparations (e.g. whole cell lysate). This antibody can be used for WB of enriched (e.g. immunoprecipitated) sources of FGD1.

    Restrictions
    For Research Use only
  • Concentration
    1000 μg/mL
    Buffer
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % 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
    Date de péremption
    12 months
  • Antigène
    FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))
    Autre désignation
    FGD1 (FGD1 Produits)
    Synonymes
    anticorps AAS, anticorps FGDY, anticorps MRXS16, anticorps ZFYVE3, anticorps FYVE, RhoGEF and PH domain containing 1, anticorps FGD1, anticorps Fgd1, anticorps fgd1
    Sujet
    Background: The gene FGD1 encodes for FYVE, RhoGEF and PH domain-containing protein 1. The encoded protein specifically binds to the Rho family GTPase Cdc42Hs. Defects in this gene are the cause of faciogenital dysplasia and X-linked mental retardation, syndromatic 16 [taken from NCBI Entrez Gene (Gene ID: 2245)].
    ID gène
    2245
    UniProt
    P98174
    Pathways
    Neurotrophin Signaling Pathway
Vous êtes ici: