Recombinant Mouse Coagulation Factor XIV/Protein C, CF Summary
Details of Functionality |
Measured by its ability to cleave the fluorogenic peptide substrate, Boc-beta -benzyl-DPR-AMC. The specific activity is >125 pmol/min/µg, as measured under the described conditions. |
Source |
Chinese Hamster Ovary cell line, CHO-derived mouse Coagulation Factor XIV/Protein C protein Ile19-Leu460 (pro) & Ala42-Leu460 (mature), both with a C-terminal 10-His tag |
Accession # |
|
N-terminal Sequence |
Ile19 & Ala42 |
Structure / Form |
Pro and Mature forms |
Protein/Peptide Type |
Recombinant Enzymes |
Gene |
Proc |
Purity |
>90%, by SDS-PAGE under reducing conditions and visualized by silver stain |
Endotoxin Note |
<1.0 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
49 kDa (Pro) & 48 kDa (Mature). 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 |
70 kDa, 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 Sodium Acetate and NaCl. |
Purity |
>90%, by SDS-PAGE under reducing conditions and visualized by silver stain |
Assay Procedure |
- Activation Buffer: 50 mM Tris, 10 mM CaCl2, 150 mM NaCl, 0.05% (w/v) Brij-35, pH 7.5 (TCNB)
- Assay Buffer: 50 mM Tris, 10 mM CaCl2, 150 mM NaCl, 0.01% (w/v) Brij-35, pH 8.5
- Recombinant Mouse Coagulation Factor XIV/Protein C (rmPROC) (Catalog # 4885-SE)
- Bacterial Thermolysin (Thermolysin) (Catalog # 3097-ZN)
- 1,10 phenanthroline (Sigma, Catalog # 320056), 0.6 M stock in DMSO
- Substrate: BOC-beta -benzyl-Asp-Pro-Arg-AMC (Bachem, Catalog # I-1560), 10 mM in DMSO
- F16 Black Maxisorp Plate (Nunc, Catalog # 475515)
- Fluorescent Plate Reader (Model: SpectraMax Gemini EM by Molecular Devices) or equivalent
- Dilute rmPROC to 200 µg/mL in Activation Buffer.
- Dilute Thermolysin to 10 µg/mL in Activation Buffer.
- Combine 25 µL of the diluted rmPROC and 25 µL of the diluted Thermolysin.
- Incubate at 37 °C for 2 hours.
- Dilute 1,10 phenanthroline to 5 mM in Assay Buffer.
- Add 200 µL of 5 mM 1,10 phenanthroline to the reaction mixtures to stop the Thermolysin activation.
- Dilute rmPROC to 2 µg/mL in Assay Buffer.
- Dilute Substrate to 200 µM in Assay Buffer.
- Load 50 µL of 2 µg/mL rmPROC into a plate, and start the reaction by adding 50 µL of 200 µM Substrate.
- Include a Substrate Blank containing 50 µL Assay Buffer and 50 µL of 200 µM Substrate.
- Read at excitation and emission wavelengths of 380 nm and 460 nm (top read), respectively, in kinetic mode for 5 minutes.
- Calculate specific activity:
Specific Activity (pmol/min/µg) = |
Adjusted Vmax* (RFU/min) x Conversion Factor** (pmol/RFU) |
amount of enzyme (µg) |
*Adjusted for Substrate Blank **Derived using calibration standard 7-Amino, 4-Methyl Coumarin (AMC) (Sigma, Catalog # A-9891). Per Well:
- rmPROC: 0.100 µg
- Substrate: 100 µM
|
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Mouse Coagulation Factor XIV/Protein C, CF
Background
Protein C is a vitamin K-dependent serine protease synthesized in the liver as a single-chain precursor, which is then proteolytically processed to two disulfide-linked chains (1). The light chain consists of a Gla (gamma-carboxy-glutamate) domain and two EGF-like domains. The heavy chain consists of an activation peptide (aa 199‑212) and serine protease domain (aa 213‑449). Physiologically, Protein C is converted to the active form by thrombin, which releases the activation peptide. Protein C plays a key role in anticoagulation, cleaving factors VIIIa and Va to inactivate them. This anticoagulation activity can be enhanced by a presence of a cofactor such as protein S. In hereditary thrombophilia, Protein C deficiency is caused by a genetic mutation that affects Protein C activity. A severe recessive form may result in massive thrombosis fatal to patient.
- Shen, L. and Dahlbäck, B. (2004) in Handbook of Proteolytic Enzymes, Barrett, A.J. et al. eds. pp. 1673.
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