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FGD1 anticorps (AA 700-800)

Cet anticorps anti-FGD1 est un anticorps Lapin Polyclonal détectant FGD1 dans WB, IHC et IF. Adapté pour Humain.
N° du produit ABIN7267284

Aperçu rapide pour FGD1 anticorps (AA 700-800) (ABIN7267284)

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
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Épitope

    • 4
    • 3
    • 1
    AA 700-800

    Fonction

    FGD1 Rabbit pAb

    Séquence

    LLNSTNREDE DTPPNSPNVD LGKRAPTPIR EKEVTMCMRC QEPFNSITKR RHHCKACGHV VCGKCSEFRA RLVYDNNRSN RVCTDCYVAL HGVPGSSPAC S

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthetic peptide corresponding to a sequence within amino acids 700-800 of human FGD1 (NP_004454.2).

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000,IHC,1:50 - 1:100,IF,1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

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

    Autre désignation

    FGD1

    Sujet

    This gene encodes a protein that contains Dbl (DH) and pleckstrin (PH) homology domains and is similar to the Rho family of small GTP-binding proteins. The encoded protein specifically binds to the Rho family GTPase Cdc42Hs and can 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. Defects in this gene are the cause of faciogenital dysplasia and X-linked mental retardation, syndromatic 16.,FGD1,AAS,FGDY,MRXS16,ZFYVE3,FYVE,Signal Transduction,G protein signaling,G-Protein-Coupled Receptors(GPCR),Cell Biology & Developmental Biology,Cytoskeleton,Microfilaments,FGD1

    Poids moléculaire

    106kDa

    ID gène

    2245

    UniProt

    P98174

    Pathways

    Neurotrophin Signaling Pathway
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