protein

Recombinant Vascular Endothelial Growth Factor-E (Orf Virus)

MBS142140

0.002 mg

140 USD

Recombinant Protein

Recombinant Vascular Endothelial Growth Factor-E (Orf Virus)

Vascular Endothelial Growth Factor-E

VEGF E (Orf Virus); Vascular Endothelial Growth Factor-E Recombinant (Orf Virus); VEGF E (Orf Virus)

Vascular endothelial growth factor homolog; Vascular endothelial growth factor homolog

VEGF

A2R

VEGFH_ORFN2

E Coli

133

Greater than 90.0% as determined by: (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE.

The protein was lyophilized from a concentrated (1mg/ml) solution containing PBS pH-7.4. Sterile Filtered White lyophilized (freeze-dried) powder.

1mg/ml

Lyophilized Vascular Endothelial Growth Factor-E Orf Virus although stable at room temperature for 3 weeks, should be stored desiccated below -18 degree C. Upon reconstitution VEGF E -OV should be stored at 4 degree C between 2-7 days and for future use below -18 degree C.Please prevent freeze-thaw cycles.

Solubility: The lyophilized VEGF-E is soluble in water and most aqueous buffers. The lyophilized Vascular Endothelial Growth Factor-E (Orf Virus) should be reconstituted in PBS or medium containing at least 0.1% human or bovine serum albumin to a concentration not lower than 50 ug/ml. Biological Activity: The ED50 for stimulation of 3H-thymidine incorporation and cell proliferation by human umbilical vein endothelial cells for VEGF-E Orf Virus has been determined to be in the range of 5 - 20 ng/ml, corresponding to a specific activity of 2 x 105 Units/mg.

CYTOKINES AND GROWTH FACTORS; Growth Factors; VEGF

Description: A DNA sequence encoding the mature variant of ovVEGF-E isolate D1701 (Dehio et al., 1999; GenBank accession No. AF106020) was expressed in E Coli as a 132 amino acid residue fusion protein with an N-terminal His-tag sequence and a thrombin cleavage site. Recombinant VEGF-E homodimer was dimerized in vitro and has a predicted mass of approximately 35 kDa. Based on sequence similarity to VEGF-A, a gene encoding a VEGF homologue has recently been discovered in the genome of Orf virus (OV) (Lyttle et al., 1994). Different isolates of Orf virus show significant amino acid sequence similarity to VEGF-A and described as a viral virulence factor that appears to be derived from captured host genes. All eight cysteine residues of the central cysteine knot motif characteristic of members of the VEGF family are conserved among other residues in the VEGF-E proteins (Dehio et al., 1999; Wise et al., 1999). Alignment of all mammalian VEGF sequences indicated that VEGF-E is distinct from the previously described VEGFs but most closely related to VEGF-A. Like VEGF-A, VEGF-E was found to bind with high affinity to VEGF receptor-2 (KDR) resulting in receptor autophosphorylation, whilst in contrast to VEGF-A, VEGF-E can not bind to VEGF receptor-1 (Flt-1). Furthermore VEGF-E can also not bind to VEGF receptor-3 (FLT-4). Therefore VEGF-E is a potent angiogenic factor selectively binding to VEGF receptor 2/KDR.

1718158

P52584.1

P52584

14,715 Da

0.002 mg

140 USD

0.01 mg

205

1 mg

6745