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Recombinant Human Proprotein Convertase 9/PCSK9 Protein, CF

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When Recombinant Human LDLR (2148-LD/CF) is immobilized at 1 µg/mL (100 µL/well), Biotinylated Recombinant Human Proprotein Convertase 9/PCSK9 His-tag Avi-tag Protein (Catalog # AVI3888) binds with an ED50 of ...read more
2 μg/lane of Biotinylated Recombinant Human Proprotein Convertase 9/PCSK9 His-tag Avi-tag Protein (Catalog # ) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by ...read more

Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Human Proprotein Convertase 9/PCSK9 Protein, CF Summary

Additional Information
Biotinylated His-tag Avi-tag
Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Human LDLR (Catalog # 2148-LD/CF) is immobilized at 1 µg/mL (100 µL/well), Biotinylated Recombinant Human Proprotein Convertase 9/PCSK9 His-tag Avi-tag (Catalog # AVI3888) binds with an ED50 of 0.150-1.20 µg/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived human Proprotein Convertase 9/PCSK9 protein
Gln31-Gln152 (pro domain), Ser153-Gln692 (mature form) with a C-terminal 6-His and Avitag
Accession #
N-terminal Sequence
Gln32 (pro domain) & Ser153 (mature form)
Structure / Form
Mature form Biotinylated via Avi-tag & prodomain
Protein/Peptide Type
Recombinant Enzymes
Purity
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
14 kDa & 60 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
18-21 & 62-69, under reducing conditions

Packaging, Storage & Formulations

Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 6 months from date of receipt, -20 to -70 °C as supplied.
  • 3 months, -20 to -70 °C under sterile conditions after opening.
Buffer
Supplied as a 0.2 μm filtered solution in Tris, NaCl and Glycerol.
Purity
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.

Notes

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

Alternate Names for Recombinant Human Proprotein Convertase 9/PCSK9 Protein, CF

  • EC 3.4.21
  • EC 3.4.21.111
  • FH3
  • FH3neural apoptosis regulated convertase 1
  • FHCL3
  • HCHOLA3
  • hypercholesterolemia, autosomal dominant 3
  • LDLCQ1
  • NARC1
  • NARC-1
  • NARC-1convertase subtilisin/kexin type 9 preproprotein
  • NARC1EC 3.4.21.-
  • Neural apoptosis-regulated convertase 1
  • PC9
  • PCSK9
  • Proprotein Convertase 9
  • proprotein convertase subtilisin/kexin type 9
  • Subtilisin/kexin-like protease PC9

Background

PCSK9 (proprotein convertase subtilisin kexin 9), also known as NARC-1, is a member of the proteinase K subfamily of subtilisin-related serine endoproteases. It is highly expressed in the liver, intestine, and kidney and plays an important role in regulating LDL R expression and circulating cholesterol levels (1). PCSK9 is synthesized as precursor protein that is autocatalytically cleaved in the endoplasmic reticulum to generate a 14 kDa prodomain and a 60 kDa catalytic domain (2). Within the secretion pathway, the prodomain remains associated with and functions as a chaperone for the catalytic domain (2). Although the other members of the proprotein convertase family demonstrate activity on several downstream targets, PCSK9 protease activity has only been demonstrated through its autocatalytic processing (3). PCSK9 plays a key role in the regulation of cholesterol metabolism by binding to hepatic LDL R, LRP-1, VLDL R, and Apolipoprotein E R2 and promoting their lysosomal degradation instead of recycling to the plasma membrane (4-7). It can also regulate cholesterol and triglyceride handling in the intestine and adipose tissue (8-10). These reported functions create significant interest in PCSK9 as a pharmacological target in cardiovascular disease (11). PCSK9 has been reported to interact with non-LDR targets as well, including mediators of inflammation and immunological processes (12).
  1. Schulz, R. et al. (2015) Basic Res. Cardiol. 110:4.
  2. Benjannet, S. et al. (2004) J. Biol. Chem. 279:48865.
  3. Naureckiene, S. et al. (2003) Arch. Biochem. Biophys. 420:55.
  4. Zhang, D.W. (2007) J. Biol. Chem. 282:18602.
  5. DeVay, R.M. et al. (2013) J. Biol. Chem. 288:10805.
  6. Canuel, M. et al. (2013) PLoS One 8:e64145.
  7. Poirier, S. et al. (2008) J. Biol. Chem. 283:2363.
  8. Levy, E. et al. (2013) Atherosclerosis 227:297.
  9. Le May, C. et al. (2013) Arterioscler. Thromb. Vasc. Biol. 33:1484.
  10. Roubtsova, A. et al. (2011) Arterioscler. Thromb. Vasc. Biol. 31:785.
  11. Chen, B. et al. (2019) Curr.Top Med. Chem. 19:1790.
  12. Dixon, D.L. et al. (2016) J. Clin. Lipidol. 10:1073. 

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