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FGD1 anticorps

L’anticorps Lapin Polyclonal anti-FGD1 a été validé pour WB et ELISA. Il convient pour détecter FGD1 dans des échantillons de Humain.
N° du produit ABIN2460269

Aperçu rapide pour FGD1 anticorps (ABIN2460269)

Antigène

Voir toutes FGD1 Anticorps
FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))

Reactivité

  • 9
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Humain

Hôte

  • 9
Lapin

Clonalité

  • 9
Polyclonal

Conjugué

  • 9
Cet anticorp FGD1 est non-conjugé

Application

  • 8
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Purification

    Antibody is purified by peptide affinity chromatography method.

    Immunogène

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FGD1.
  • Indications d'application

    FGD1 antibody can be used for detection of FGD1 by ELISA at 1:312500. FGD1 antibody can be used for detection of FGD1 by western blot at 2.0 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Concentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Conseil sur la manipulation

    As with any antibody avoid repeat freeze-thaw cycles.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store FGD1 antibody at -20 °C.
  • Antigène

    FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))

    Autre désignation

    FGD1

    Sujet

    FGD1 contains Dbl (DH) and pleckstrin (PH) homology domains. It can bind specifically to the Rho family GTPase Cdc42Hs and stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. FGD1 has an essential role in embryonic development, and FGD1 gene mutations result in the human developmental disorder, Aarskog-Scott syndrome.

    Poids moléculaire

    107 kDa

    ID gène

    2245

    NCBI Accession

    NP_004454

    UniProt

    P98174

    Pathways

    Neurotrophin Signaling Pathway
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