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Recombinant Human Serpin F1/PEDF Protein, CF

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Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

Order Details

Recombinant Human Serpin F1/PEDF Protein, CF Summary

Details of Functionality
Measured by its ability to enhance the adhesion of Saos‑2 human osteosarcoma cells to bovine Collagen I coated plate. Eth, E.K. et al. (2007) Cancer Gene Therapy. 14:616. The ED50 for this effect is 0.15-0.75 μg/mL.
Source
Mouse myeloma cell line, NS0-derived human Serpin F1/PEDF protein
Met1-Pro418, with a C-terminal 6-His tag
Accession #
N-terminal Sequence
Gln20 is predicted: no results obtained, sequencing might be blocked
Structure / Form
Monomer
Protein/Peptide Type
Recombinant Proteins
Gene
SERPINF1
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<1.0 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
45 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
45-53 kDa, reducing conditions
Publications
Read Publications using
1177-SF in the following applications:

Packaging, Storage & Formulations

Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in Tris and NaCl.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 250 μg/mL in 20 mM Tris-HCl, pH 8.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Human Serpin F1/PEDF Protein, CF

  • Cell proliferation-inducing gene 35 protein
  • EPC-1
  • EPC-1PIG35
  • PEDF
  • PEDFpigment epithelium-derived factor
  • pigment epithelium derived factor), member 1
  • proliferation-inducing protein 35
  • serine (or cysteine) proteinase inhibitor, clade F (alpha-2 antiplasmin
  • Serpin F1
  • serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epitheliumderived factor), member 1

Background

Serpin F1 (SERine Proteinase Inhibitor‑clade F1; also PEDF/Pigment Epithelium‑Derived Factor, EPC‑1 and PIG35) is a monomeric, 52‑55 kDa secreted phosphoglycoprotein that belongs to the clade F subfamily, serpin superfamily of proteinase inhibitors (1‑4).  Serpins in general form two groups: one that demonstrates protease inhibition, and another (containing Serpin F1) whose members show no protease inhibition, but which act as chaperones and circulating transporters (2)   Serpin F1 is synthesized as a 418 amino acid (aa) precursor that contains a 19 aa signal sequence plus a 399 aa mature region that shows a pyroglutamate at Gln20 (5, 6, 7).  Like other serpins, it contains three beta ‑sheets, 8‑10 alpha ‑helices, and a C‑terminal RCL (reactive center loop).  Unlike other serpins with Ser protease inhibiting activity, the RCL of Serpin F1 does not undergo a conformational change upon target protease cleavage, a prerequisite for anti‑protease activity.  Such cleavage does, however, generate a 46 kDa fragment that possesses nonprotease‑associated (i.e.‑neurotrophic) bioactivity (8).  Phosphorylation occurs both intracellularly and extracellularly. Intracellularly, PKA phosphorylates Ser227, promoting anti‑angiogenic activity.  Extracellularly, CK2 phosphorylates Ser24 and Ser114, promoting neurotrophic activity (9).  Multiple sites have been identified and associated with distinct biological activities.  Amino acids 63‑70 constitute a functional NLS, and a 36 kDa Serpin F1 isoform has been reported in the nucleus (10).  In addition, lipase activity (perhaps a consequence of receptor binding) has been mapped to aa 78‑141, anti‑angiogenic activity to aa 20‑70 plus Ser114 and Ser227, neurotrophic activity to aa 32‑141, and heparin binding to aa 121‑149 (4).  Mature human Serpin F1 shares 86% aa sequence identity with mouse Serpin F1.

Serpin F1 is known to be synthesized by multiple cell types, including retinal pigment epithelium (RPE), fibroblasts, mammary epithelium, preadipocytes and adipocytes, hepatocytes, osteoblasts and osteoclasts (1, 2, 11‑15).  This diversity of cell types reflects its many activities, among which are neuroprotection, lipolysis, antiangiogenesis, and anticarcinogenesis (2‑4).  Much work has been done with RPE, a cell type that is known to both provide neuroprotection and block angiogenesis.  On the neuroprotection side, Serpin F1 binding to an 83 kDa, 4‑transmembrane PEDF receptor (also known as PNPLP2 and TTS‑2.2) results in the activation of receptor‑associated PLA2 activity.  This activity is directed towards RPE membrane triglycerides that contain a dietary omega ‑3 fatty acid called DHA.  Once released via lipase activity, DHA is converted into NDP1, a neuroprotective lipid that acts on the surrounding neural complex (2, 16‑18).  RPE‑derived Serpin F1 also minimizes retinal vascularization.  This apparently occurs through a variety of mechanisms.  First, Serpin F1 binds to PEDFR on endothelial cells (EC), generating PPAR gamma ligands via EC CYP450.  These ligands activate PPAR gamma induces p53 and subsequent EC apoptosis (19, 20).  Second, Serpin F1 apparently binds the 67 kDa laminin receptor (LR) on EC.  This activates caspase‑3 with the initiation of an apoptotic program (21).  Finally, Serpin F1 interfers with VEGF signaling.  This appears to happen through at least two mechanisms.  First, there is a direct competitive binding of Serpin F1 to the EC VEGFR2, blocking VEGF signaling (22).  Second, Serpin F1 binding to EC activates membrane gamma ‑secretase, resulting in the proteolytic cleavage of both VEGFR1 and R2, which abrogates signaling and creates a soluble receptor for VEGF (22, 23, 24).

  1. Tombran-Tink, J. et al. (1991) Exp. Eye Res. 53:411.
  2. Broadhead, M.L. et al. (2010) Growth Factors 28:280.
  3. Filleur, S. et al. (2009) J. Cell. Biochem. 106:769.
  4. Kawaguchi, T. et al. (2010) Curr. Mol. Med. 10:302.
  5. Steele, F.R. et al. (1993) Proc. Natl. Acad. Sci. USA 90:1526.
  6. SwissProt # P36995.
  7. Peterson, S.V. et al. (2003) Biochem. J. 374:199.
  8. Wu, Y-Q. et al. (1996) Invest. Ophthalmol. Vis. Sci. 37:1984.
  9. Maik-Rachline, G. et al. (2005) Blood 105:670.
  10. Anguissola, S. et al. (2011) PLoS ONE 6:e26234.
  11. Lashbrook, B.L. and J.J. Steinle (2005) Auton. Neurosci. 121:33.
  12. Cai, J. et al. (2006) Clin. Cancer Res. 12:3510.
  13. Tombran-Tink, J. and C.J. Barnstable (2004) Biochem. Biophys. Res. Commun. 316:573.
  14. Zvonic, S. et al. (2007) Mol. Cell. Proteomics 6:18.
  15. Sawant, S. et al. (2004) Biochem. Biophys. Res. Commun. 325:408.
  16. Notari, L. et al. (2006) J. Biol. Chem. 281:38022.
  17. Mukherjee, P.K. et al. (2004) Proc. Natl. Acad. Sci. USA 101:8491.
  18. Mukherjee, P.K. et al. (2007) Proc. Natl. Acad. Sci. USA 104:13152.
  19. Ho, T-C. et al. (2007) Cardiovasc. Res. 76:213.
  20. Liu, Y. et al. (2004) Circulation 110:1128.
  21. Bernard, A. et al. (2009) J. Biol. Chem. 284:10480.
  22. Zhang, S.X. et al. (2006) J. Mol. Endocrinol. 37:1.
  23. Ablonczy, Z. et al. (2009) J. Biol. Chem. 284:30177.
  24. Cai, J. et al. (2006) J. Biol. Chem. 281:3604.

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Publications for Serpin F1/PEDF (1177-SF)(4)

We have publications tested in 3 confirmed species: Human, Mouse, Rat.

We have publications tested in 1 application: Bioassay.


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(4)
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(3)
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(2)
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Bioinformatics

Gene Symbol SERPINF1
Uniprot