Recombinant Mouse QSOX1/Quiescin Q6 Protein, CF

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Product Details

Summary
Reactivity MuSpecies Glossary
Applications Enzyme Activity
Format
Carrier-Free

Order Details

Recombinant Mouse QSOX1/Quiescin Q6 Protein, CF Summary

Details of Functionality
Measured by its ability to produce hydrogen peroxide during the oxidation of Dithiothreitol (DTT). The specific activity is >1,200 pmol/min/μg, as measured under the described conditions.
Source
E. coli-derived mouse QSOX1/Quiescin Q6 protein
Ser36-Ala550
with an N-terminal Met and 6-His tag
Accession #
N-terminal Sequence
Met
Protein/Peptide Type
Recombinant Enzymes
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
  • Enzyme Activity
Theoretical MW
59 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
56 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 Tris and NaCl.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Assay Procedure
  • Assay Buffer: 50 mM Sodium Phosphate, pH 7.5
  • Recombinant Mouse QSOX1/Quiescin Q6 (rmQSOX1) (Catalog # 9257-QS)
  • Coupling Enzyme:  Horseradish Peroxidase (HRP), 250-330 U/mg (Sigma, Catalog # P8375), 250 units/mL stock in 0.1 M Sodium Phosphate, pH 8.0
  • Substrate Component 1: Dithiothreitol (DTT) (Amresco, Catalog # 0281), 1 M stock in deionized water
  • Substrate Component 2: Amplex® Ultra Red (AUR) (Invitrogen, Catalog # A36006), 10 mM stock in DMSO
  • F15 Black Maxisorp Plate (Nunc, Catalog # 475515)
  • Fluorescent Plate Reader (Model: SpectraMax Gemini EM by Molecular Devices) or equivalent
  1. Dilute rmQSOX1 to 1 ng/μL in Assay Buffer.
  2. Prepare a Substrate Mixture containing 100 µM AUR, 2 units/mL HRP and 300 µM DTT in Assay Buffer. Make sure to add the DTT component right before reading the plate.
  3. Load 50 μL of 1 ng/μL rmQSOX1 into the plate, and start the reaction by adding 50 μL of Substrate Mixture. Include a Substrate Blank containing 50 μL of Assay Buffer and 50 μL of Substrate Mixture.
  4. Read at excitation and emission wavelengths of 544 nm and 590 nm in kinetic mode for 5 minutes. Note: A cutoff must be set at a wavelength of 570 nm.
  5. 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 a fluorescent standard prepared by incubating 50 µM AUR, 1 unit/mL HRP and 150 µM DTT and a curve of Hydrogen Peroxide (Sigma, Catalog # H1009) in Assay Buffer.  Use this oxidized AUR curve to determine the conversion factor.

Per Well:
  • rmQSOX1: 0.05 μg
  • DTT: 150 µM
  • HRP: 1 unit/mL
  • AUR: 50 µM

Notes

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

Alternate Names for Recombinant Mouse QSOX1/Quiescin Q6 Protein, CF

  • EC 1.8.3.2
  • FLJ34858
  • HQSOX
  • Q6
  • QSCN6
  • QSOX1
  • quiescin Q6 sulfhydryl oxidase 1
  • Quiescin Q6
  • sulfhydryl oxidase 1
  • Sulfhydryl Oxidase-1

Background

Sulfhydryl Oxidase-1 (QSOX1) is an enzyme that contains thioredoxin and sulfhydryl oxidase domains (1-3). It is synthesized with a C-terminal transmembrane segment, but soluble secreted forms can be generated by alternative splicing or proteolytic shedding within the Golgi (4). Within the region encompassing both enzymatic domains and the central region, mouse QSOX1 shares 79% and 92% aa sequence identity with human and rat QSOX1, respectively. It plays a role in nascent protein folding by mediating disulfide oxidation (4-6). This activity is required for Laminin incorporation into the extracellular matrix (7). QSOX1 is up-regulated in many cancers and supports tumor cell proliferation and invasion (1, 8).
  1. Lake, D.F. and D.O. Faigel (2014) Antioxid. Redox. Signal. 21:485.
  2. Kodali, V.K. and C. Thorpe (2010) Antioxid. Redox Signal. 13:1217.
  3. Matsuba, S. et al. (2002) J. Dermatol. Sci. 30:50.
  4. Rudolf, J. et al. (2013) Biochem. J. 454:181.
  5. Heckler, E.J. et al. (2008) Biochemistry 47:4955.
  6. Alon, A. et al. (2012) Nature 488:414.
  7. Ilani, T. et al. (2013) Science 341:74.
  8. Katchman, B.A. et al. (2011) Mol. Cancer Res. 9:1621.

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