VEGF-A (VEGF120) Mouse Protein
Specifications
| Product Data | |
| Species | Mouse |
|---|---|
| Expression Host | E. coli |
| Expression cDNA Clone or AA Sequence | |
| Predicted MW | 28.2 kDa |
| Purity | >95% by SDS-PAGE and silver stain |
| Presentation State | Purified |
| Buffer | Presentation State: Purified State: Lyophilized protein Buffer System: 50 mM Acetic Acid Stabilizer: None |
| Bioactivity | Biological: Determined by the dose-dependent stimulation of the proliferation of human umbilical vein endothelial cells (HUVEC) using a concentration range of 1-10 ng/ml. |
| Endotoxin | < 0.1 ng/µg of VEGF120 |
| Reconstitution Method | The lyophilized VEGF120 is soluble in water and most aqueous buffers. The lyophilized VEGF120 should be reconstituted in 50mM acetic acid or medium containing at least 0.1% human or bovine serum albumin to a concentration not lower than 50μg/ml. |
| Preparation | Lyophilized protein |
| Protein Description | Recombinant Murine Vascular Endothelial Growth Factor120 |
| Note | Range: 1.0-10.0 ng/ml Protein RefSeq: NP 001020421 mRNA RefSeq: NM 001025250 |
| Storage | The lyophilized protein is stable at 2-8°C for up to 1 week or at -20°C for longer. Following reconstitution store (in aliquots) at -20°C. Avoid repeated freezing and thawing. |
| Stability | Shelf life: one year from despatch. |
| Shipping | Ambient |
| Reference Data | |
| RefSeq | NP_001020421 |
| Locus ID | 22339 |
| UniProt ID | Q00731 |
| Cytogenetics | 17 22.79 cM |
| Synonyms | VEGFA, VEGF, VPF, Vascular endothelial growth factor A, Vascular permeability factor |
| Summary | This gene is a member of the PDGF/VEGF growth factor family. It encodes a heparin-binding protein, which exists as a disulfide-linked homodimer. This growth factor induces proliferation and migration of vascular endothelial cells, and is essential for both physiological and pathological angiogenesis. Disruption of this gene in mice resulted in abnormal embryonic blood vessel formation. This gene is upregulated in many known tumors and its expression is correlated with tumor stage and progression. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. There is also evidence for alternative translation initiation from upstream non-AUG (CUG) codons resulting in additional isoforms. A recent study showed that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is antiangiogenic. Expression of some isoforms derived from the AUG start codon is regulated by a small upstream open reading frame, which is located within an internal ribosome entry site.provided by RefSeq, Nov 2015 |
| Protein Categories | Cytokines, Endocrine and metabolic diseases, Growth Factors, Intracellular Proteins, Membrane Proteins, Nervous system Diseases, Secreated Proteins |
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*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen
complexities in the preparation of your product. International customers may expect an additional 1-2 weeks
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