Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

AGGF1 Antikörper

Der Kaninchen Polyklonal Anti-AGGF1-Antikörper wurde für WB und IHC validiert. Er ist geeignet, AGGF1 in Proben von Human zu detektieren.
Produktnummer ABIN7539232

Kurzübersicht für AGGF1 Antikörper (ABIN7539232)

Target

Alle AGGF1 Antikörper anzeigen
AGGF1 (Angiogenic Factor with G Patch and FHA Domains 1 (AGGF1))

Reaktivität

  • 41
  • 29
  • 9
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 63
  • 6
Kaninchen

Klonalität

  • 66
  • 4
Polyklonal

Konjugat

  • 46
  • 6
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser AGGF1 Antikörper ist unkonjugiert

Applikation

  • 65
  • 28
  • 26
  • 17
  • 16
  • 13
  • 13
  • 7
  • 7
  • 3
  • 3
  • 2
  • 2
Western Blotting (WB), Immunohistochemistry (IHC)
  • Verwendungszweck

    AGGF1 antibody

    Aufreinigung

    Protein A purified

    Immunogen

    recombinant human AGGF1 (fragment)

    Isotyp

    IgG
  • Applikationshinweise

    WB: Use 1-5 μg/mL, IHC: 1:50

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Centrifuge vial prior to opening. Reconstitute in sterile water to a concentration of 0.1-1.0 mg/mL.

    Buffer

    PBS

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    The lyophilized antibody is stable for at least 2 years at -20°C. After sterile reconstitution the antibody is stable at 2-8°C for up to 6 months. Frozen aliquots are stable for at least 6 months when stored at -20°C. Addition of a carrier protein or 50% glycerol is recommended for frozen aliquots.

    Haltbarkeit

    24 months
  • Target

    AGGF1 (Angiogenic Factor with G Patch and FHA Domains 1 (AGGF1))

    Andere Bezeichnung

    AGGF1

    Hintergrund

    Angiogenic factor VG5Q, hVG5Q, G patch domain-containing protein 7, Vasculogenesis gene on 5q protein,AGGF1, also known as VG5Q, was identified by its association with Klippel Trenaunay syndrome (KTS), a congenital vascular morphogenesis disorder (1 3). AGGF1 is expressed by vascular endothelial cells in many tissues (1). It appears to be secreted and promotes endothelial cell proliferation following interactions with endothelial cell surfaces (1). AGGF1 also directly interacts with TWEAK (1), a TNF superfamily ligand with angiogenic properties (8). It was shown that AGGF1 is involved in establishing venous identity in zebrafish embryos. Overexpression of AGGF1 led to increased angiogenesis and increased lumen diameter of veins, whereas knockdown of AGGF1 expression resulted in defective vasculogenesis and angiogenesis. Overexpression of AGGF1 increased expression of venous markers (e.g. VEGFR-3/FLT4), but had little effect on arterial markers (e.g. Notch5). Knockdown of AGGF1 expression resulted in a loss of venous identity (loss of expression of VEGFR-3/FLT4, Ephb4 and Dab2), but had no effect on the expression of arterial development. It was further shown that AGGF1 activates AKT, and that decreased AGGF1 expression inhibits AKT activation. Overexpression of constitutively active AKT rescues the loss of venous identity caused by AGGF1 downregulation. These results indicate that AGGF might be an angiogenic factor with an important role in the specification of vein identity and suggests that AGGF1-mediated AKT signaling is responsible for establishing venous cell fate.

    Gen-ID

    55109

    UniProt

    Q8N302
Sie sind hier:
Chat with us!