Rabbit Anti-Human AGGF1
Slide this table
| Cat-Nr. | 102-PA13S |
| Size | 100 µg |
| Price | 185 € |
| Category | Polyclonal Antibody |
| Clone Nr. | Rabbit IgG |
| Isotype | Rabbit IgG |
| Species Reactivity | Human |
| Formulation | lyophilized |
| Buffer | PBS |
| Reconstitution | Centrifuge vial prior to opening. Reconstitute in sterile water to a concentration of 0.1-1.0 mg/ml. |
| Stability and Storage | 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. |
| Preparation | Produced from sera of rabbits immunized with highly pure recombinant humanAGGF1 fragement as the immunizing antigen. Anti-human AGGF1 was purified by affinity chromatography with immobilized Protein A. |
| Antigen | recombinant human AGGF1 (fragment) |
| Application | WB, IHC |
| Synonyms | Angiogenic factor VG5Q, hVG5Q, G patch domain-containing protein 7, Vasculogenesis gene on 5q protein |
| Description | 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. |
| Uniprot ID | Q8N302 |
| Protein RefSeq | NP_060516.2. |
| mRNA RefSeq | NM_018046.4. |
Figures
Immunofluorescence staining of cryo-sections of human placental tissue (4% PFA overnight) with [A] rabbit AGGF1 (1:50) [Cat# 102-PA13] and [B] control without primary antibody. Counter staining of nuclei with Dapi (blue).
The experiment was performed by the research group of Prof. Dr. J. Wilting, University Göttingen, Germany.
Western Blot analysis with a recombinant human AGGF1 fragment using a rabbit polyclonal anti-human AGGF1 [Cat# 102-PA13].
All prices plus VAT + possible delivery charges