>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
44 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
43 kDa, reducing conditions
Publications
Read Publication using 9070-CK in the following applications:
Plate Reader (Model: SpectraMax Plus by Molecular Devices) or equivalent
Prepare 1X Assay Buffer by diluting 10X stocks 10-fold with deionized water.
Dilute
1 mM Phosphate Standard provided by the Universal Kinase Activity Kit
by adding 40 µL of the 1 mM Phosphate Standard to 360 µL of 1X Assay
Buffer for a 100 µM stock. This is the first point of the standard
curve.
Complete the standard curve by performing six one-half
serial dilutions of the 100 µM Phosphate stock using 1X Assay Buffer. The standard curve has a range of 0.078 to 5 nmol per well.
Prepare a reaction mixture containing 0.4 mM ATP (supplied in kit) and 8 mM Creatine in 1X Assay Buffer.
Dilute rhCKM to 6.667 ng/µL in 1X Assay Buffer.
Dilute Coupling Phosphatase 4 (supplied in kit) to 10 µg/mL in 1X Assay Buffer.
Load 50 µL of each dilution of the standard curve into a plate. Include a curve blank containing 50 μL of 1X Assay Buffer.
Load
15 µL of the 6.667 ng/µL rhCKM into empty wells of the same plate as
the curve. Include a Control containing 15 µL of 1X Assay Buffer.
Add 10 µL of 10 µg/mL Coupling Phosphatase 4 to wells containing enzyme and control, excluding the standard curve.
Add 25 µL of reaction mixture to the wells, excluding the standard curve.
Cover the plate with a plate sealer and incubate at room temperature for 10 minutes.
Add 30 µL of the Malachite Green Reagent A to all wells. Mix briefly.
Add 100 µL of deionized water to all wells. Mix briefly.
Add 30 µL of the Malachite Green Reagent B to all wells. Mix and incubate for 20 minutes at room temperature.
Read plate at 620 nm (absorbance) in endpoint mode.
Calculate specific activity:
Specific Activity (pmol/min/µg) =
Phosphate released* (nmol) x (1000 pmol/nmol)
Incubation time (min) x amount of enzyme (µg) x coupling rate**
*Derived from the phosphate standard curve using linear or 4-parameter fitting and adjusted for Control. ** The coupling rate is 0.475 under these conditions.
Per Reaction:
rhCKM: 0.1 µg
Coupling Phosphatase 4: 0.1 µg
Creatine: 4 mM
ATP: 0.2 mM
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human Creatine Kinase MM/CKMM Protein, CF
CKM
CKMM
CKMMcreatine kinase M-type
Creatine Kinase Isoenzyme
Creatine kinase M chain
Creatine Kinase MM
creatine kinase, muscle
creatine kinase-M
EC 2.7.3
EC 2.7.3.2
M-CK
Background
Creatine kinase (CK) catalyzes the conversion of creatine to phosphocreatine (PCr) by consuming adenosine triphosphate (ATP) and generating adenosine diphosphate (ADP). CK reaction is reversible and thus ATP can be generated from PCr and ADP (1). In tissues and cells that consume ATP rapidly, especially skeletal muscle, but also brain, photoreceptor cells of the retina, hair cells of the inner ear, spermatozoa and smooth muscle, PCr serves as an energy reservoir for the rapid buffering and regeneration of ATP in situ, as well as for intracellular energy transport by the PCr shuttle or circuit (2). Clinically, creatine kinase is assayed in blood tests as a marker of myocardial infarction (heart attack), rhabdomyolysis (severe muscle breakdown), muscular dystrophy, autoimmune myositides and acute renal failure. Creatine kinase M (CKM), especially, is a cytoplasmic enzyme and is an important serum marker for myocardial infarction. It acts as a homodimer (MM type) in striated muscle as well as in other tissues, and forms a heterodimer (MB type) with CKB, a brain isozyme, in the heart (3). The recombinant human CKM is in the MM type and its activity is measured using a phosphatase-coupled method (4).
Trask, R.V. et al. (1988) J. Biol. Chem. 263:17142.
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