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AGGF1 Polyklonaler Antikörper

AGGF1 Polyklonal Antikörper für WB, Indirect ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus, Ratte

Anwendung

WB, Indirect ELISA

Konjugation

Unkonjugiert

Kat-Nr. : 11889-1-PBS

Synonyme

HUS84971, HSU84971, GPATCH7, GPATC7, G patch domain-containing protein 7

Filter:
  • Western Blot (WB) analysis of various lysates using AGGF1 Polyclonal antibody (11889-1-AP)

    WB analysis using 11889-1-AP (same clone as 11889-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 11889-1-AP (AGGF1 antibody) at dilution of 1:4000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 11889-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of HeLa cells using AGGF1 Polyclonal antibody (11889-1-AP)

    WB analysis of HeLa using 11889-1-AP (same clone as 11889-1-PBS)

    WB result of AGGF1 antibody (11889-1-AP; 1:3000; incubated at room temperature for 1.5 hours) with sh-Control and sh-AGGF1 transfected HeLa cells. This data was developed using the same antibody clone with 11889-1-PBS in a different storage buffer formulation.

Geprüfte Anwendungen

Produktinformation

11889-1-PBS bindet in WB, Indirect ELISA AGGF1 und zeigt Reaktivität mit human, Maus, Ratten

Getestete Reaktivität human, Maus, Ratte
Wirt / Isotyp Kaninchen / IgG
Klonalität Polyklonal
Typ Antikörper
Immunogen AGGF1 fusion protein Ag2497
Vollständiger Name angiogenic factor with G patch and FHA domains 1
Berechnetes Molekulargewicht 714 aa, 81 kDa
Beobachtetes Molekulargewicht 84-100 kDa
GenBank-ZugangsnummerBC029382
Gene symbol AGGF1
Gene ID (NCBI) 55109
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Antigen-Affinitätsreinigung
Lagerungspuffer PBS only
LagerungsbedingungenStore at -80°C. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

The angiogenic factor gene, AGGF1 (or VG5Q), is identified as a candidate susceptibility gene for Klippel-Trenaunay syndrome (KTS) which is a severe congenital disorder characterized by capillary malformations, venous malformations or varicose veins, and hypertrophy of the affected tissues. AGGF1 protein can bind to endothelial cells and promote cell proliferation. AGGF1 shows strong expression in blood vessels and is secreted as vessel formation is initiated. Regulation of AGGF1 by GATA1 may play roles in endothelial cell biology and angiogenesis.