Recombinant Mouse Kininogen HMW (HKa) Protein, CF

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Product Details

Summary
Reactivity MuSpecies Glossary
Applications Inhibition Activity
Format
Carrier-Free

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Recombinant Mouse Kininogen HMW (HKa) Protein, CF Summary

Details of Functionality
Measured by its ability to inhibit papain cleavage of a fluorogenic peptide substrate Z-FR-AMC (Catalog # ES009). The IC50 value is <5 nM, as measured under the described conditions.
Source
Mouse myeloma cell line, NS0-derived mouse Kininogen protein
Glu21-Ser661, with a C-terminal 10-His tag
Accession #
N-terminal Sequence
Glu21 (mature and heavy chains) & Ser389 (light chain)
Protein/Peptide Type
Recombinant Enzymes
Gene
Kng1
Purity
>95%, 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
  • Inhibition Activity
Theoretical MW
72 kDa (mature), 38 kDa (heavy) & 31 kDa (light).
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
120 kDa, 60 kDa, 48 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 reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in Tris and NaCl.
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Reconstitution Instructions
Reconstitute at 100 μg/mL in sterile 25 mM Tris and 150 mM NaCl, pH 7.5.
Assay Procedure
  • Activation Buffer: 50 mM Tris, 5 mM DTT, pH 7.0
  • Assay Buffer: 50 mM Tris, pH 7.0
  • Recombinant Mouse Kininogen High Molecular Weight (HKa) (rmKininogen) (Catalog # 2206-PI)
  • Papain (Sigma, Catalog # P4762)
  • Substrate: Z-Phe-Arg-AMC (Catalog # ES009), 10 mM stock in DMSO
  • F16 Black Maxisorp Plate (Nunc, Catalog # 475515)
  • Fluorescent Plate Reader (Model: SpectraMax Gemini EM by Molecular Devices) or equivalent
  1. Dilute Papain to 100 µg/mL in Activation Buffer.
  2. Incubate at room temperature for 10 minutes.
  3. Prepare a dilution curve of rmKininogen (MW: 72,313 Da) in Assay Buffer. Make the following serial dilutions: 1000, 500, 125, 62.5, 41.7, 27.8, 18.5, 9.26, 3.09, and 1.03 nM.
  4. Dilute activated Papain to 2.4 µg/mL in Assay Buffer.
  5. Mix equal volumes of the rmKininogen curve dilutions and the diluted active Papain. Include a control (in duplicate) containing Assay Buffer and the diluted active Papain.
  6. Incubate mixtures at room temperature for 10 minutes.
  7. Perform a 1/5 dilution with Assay Buffer to the incubated mixtures.
  8. Dilute Substrate to 200 µM in Assay Buffer.
  9. Load 50 µL of diluted incubated mixture into a plate, and start the reaction by adding 50 µL of 200 µM Substrate.
  10. Read at excitation and emission wavelengths of 380 nm and 460 nm, respectively, for 5 minutes in kinetic mode.
  11. Derive the 50% inhibiting concentration (IC50) value for rmKininogen by plotting RFU/min (or specific activity) vs. concentration with 4‑PL fitting.
  12. The specific activity for papain at each point may be determined using the following formula (if needed):

     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:
  • Papain: 0.012 µg
  • Substrate: 100 µM
  • rmKininogen curve: 50, 25, 6.25, 3.125, 2.09, 1.39, 0.925, 0.463, 0.155, and 0.052 nM

Notes

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

Alternate Names for Recombinant Mouse Kininogen HMW (HKa) Protein, CF

  • alpha 2-thiol Proteinase Inhibitor
  • BDK
  • BDK;BK;HAE6;HK;HMWK;Kininogen-1;KNG;KNG1
  • Kininogen
  • KNG1

Background

Kininogen, also known as alpha 2-thiol proteinase inhibitor, is a multi-function protein. There are two alternatively spliced forms, designated as the high molecular weight (HMW) and low MW (LMW) forms (1). The mouse HMW form is synthesized as a 661 amino acid residue precursor with a signal peptide (residues 1-20). The mature chain (residues 21-661) is further processed into the heavy (residues 21‑379) and the light (residues 389-661) chains. The active peptide bradykinin (residues 380-388) is released, which has a variety of functions including muscle contraction, hypotension and inflammation. The heavy chain consists of three cystatin-like domains, which are responsible for inhibiting cysteine proteases. The light chain consists of a His-rich domain, which is associated with the clotting activity. In comparison to the HMW form, the LMW Kininogen (432 residues) has the same sequence in its heavy chain and bradykinin, but a different sequence in its light chain (residues 401‑432). The LMW form is not involved in blood clotting.

  1. Takano, M. et al. (1997) Biochim. Biophys. Acta 1352:222.

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Bioinformatics

Gene Symbol Kng1
Uniprot