Recombinant Human Complement Factor H-related 4/CFHR4, CF

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When Recombinant Mouse Complement Component C3d His-tag (2655-C3) is immobilized at 2 µg/mL (100 µL/well), Recombinant Human Complement Factor H‑related 4/CFHR4 His-tag Protein (Catalog # 11300-CH) binds with an ...read more
2 μg/lane of Recombinant Human Complement Factor H-related 4/CFHR4 His-tag Protein (Catalog # 11300-CH) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® ...read more

Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

Order Details

Recombinant Human Complement Factor H-related 4/CFHR4, CF Summary

Additional Information
HEK293, His-tag
Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Mouse Complement Component C3d His-tag (Catalog # 2655-C3) is immobilized at 2 µg/mL (100 µL/well), Recombinant Human Complement Factor H-related 4/CFHR4 His-tag (Catalog # 11300-CH) binds with an ED50 of 1.50-15.0 ng/mL.
Source
Human embryonic kidney cell, HEK293-derived human Complement Factor H-related 4/CFHR4 protein
Glu20-Glu578, with a C-terminal 6-His tag
Accession #
N-terminal Sequence
Glu20
Protein/Peptide Type
Recombinant Enzymes
Purity
>95%, 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
64 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
92-103 kDa, under reducing conditions

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 with Trehalose.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 200 μg/mL in PBS.

Notes

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

Alternate Names for Recombinant Human Complement Factor H-related 4/CFHR4, CF

  • complement factor H-related protein 4
  • CFHL4
  • CFHR4
  • Complement Factor Hrelated 4
  • Complement Factor H-related 4
  • FHR4
  • FHR-4

Background

Complement factor H-related protein 4 (CFHR4) is a secreted glycoprotein member of the factor H family of glycoproteins (1). The human complement factor H protein family consists of the complement and immune regulators factor H, the factor H-like protein 1 (FHL-1) and five factor H-related proteins (FHR-1 to -5) (1). The genes of this family are located on human chromosome 1q32, which is known as the regulator of complement activation (RCA) gene clusters (2). CFHRs are exclusively composed of individually folded protein domains, termed short consensus repeats (SCRs) or complement control modules. All CFHRs, including CFHR4, are capable of binding complement factor C3b, discriminate between self and non-self cell surfaces, and have been proposed to deregulate complement activation by inhibiting interaction of CFH with C3b and C3d (1, 3). CFHR4 activates complement through its interaction with C3b (4). CFHR4 can also bind to native (pentameric) C-reactive protein (pCRP) through its first SCR domain and is suggested to promote pCRP binding to necrotic cells surfaces, thus promoting cell clearance (5).  CFHR4 is synthesized as 2 isoforms by hepatocytes and circulates in plasma. The shorter isoform, FHR4B, contains 5 of 9 SCRs. The CFHR4 product includes a duplication insertion of 247 aa and represents the longer alternative splice form termed FHR4A (6). 
  1. Skerka, C. et al. (2013) Mol. Immunol. 56:170.
  2. Diaz-Guillen, M.A. et al. (1999) Immunogenetics 49:549.
  3. Hellwage, J. et al. (1999) FEBS Lett. 462:345.
  4. Hebecker, M. and J. Jozsi (2011) J. Biol. Chem. 287:19528.
  5. Mihlan, M. et al. (2009) Mol. Immunol. 46:335.
  6. Jozsi, M. et al. (2005) Eur. J. Hum. Genet. 13:321.

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