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FGD1 Antikörper

Der Kaninchen Polyklonal Anti-FGD1-Antikörper wurde für WB und ELISA validiert. Er ist geeignet, FGD1 in Proben von Human zu detektieren.
Produktnummer ABIN2460269

Kurzübersicht für FGD1 Antikörper (ABIN2460269)

Target

Alle FGD1 Antikörper anzeigen
FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))

Reaktivität

  • 9
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Human

Wirt

  • 9
Kaninchen

Klonalität

  • 9
Polyklonal

Konjugat

  • 9
Dieser FGD1 Antikörper ist unkonjugiert

Applikation

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

    Antibody is purified by peptide affinity chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FGD1.
  • Applikationshinweise

    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.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

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

    Konzentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handhabung

    As with any antibody avoid repeat freeze-thaw cycles.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

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

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

    Andere Bezeichnung

    FGD1

    Hintergrund

    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.

    Molekulargewicht

    107 kDa

    Gen-ID

    2245

    NCBI Accession

    NP_004454

    UniProt

    P98174

    Pathways

    Neurotrophin Signalübertragung
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