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INFORMATION
| Catalog No: |
Product Description: |
Pack Size: |
| CK 10 |
CK-NAC |
10 X 1.1 ML |
| CK 30 |
CK-NAC |
10 X 3 ML |
METHOD
Kinetic method
PRINCIPLE
Creatine kinase (CK) catalyses the reaction between creatine phosphate
and ADP, giving creatine and ATP. The ATP and glucose are converted
to ADP, and glucose-6-phosphate by hexokinase. Glucose-6-phosphate
dehydrogenase (G-6-PDH) oxidises glucose-6-phosphate and reduces NAD
to NADH. The rate of NADH formation is determined photometrically
at 340 nm and is directly proportional to the CK activity in the sample.
SAMPLE:
Serum free of hemolysis, heparinised plasma, protected from light.
Stability 24 hrs at 2-8°C; 3 days at -20°C
REFERENCE VALUES
| 25 - 192 U/l (37°C) |
| 10 - 109 U/l (30°C) |
QUALITY CONTROL :
Accutestrol N - H
REAGENTS
Reagent I - Enzyme Reagent
Reagent I - Diluent
REFERENCES
Youngs et. al., Clin. Chem., 21 : 10 (1975) Moren L.G., Clin. Chem.,
23 : 1569 (1977)
REAGENT PREPARATION
Dissolve the contents of one vial of enzyme reagent with the volume
of diluent water as specified on the enzyme vial, swirl to dissolve.
|
STABILITY : 21 days at 2-8°C
AUTOMATED PARAMETERS
| Wave length |
340 nm |
| Cuvette |
1 cm |
| Reaction Temperature |
37°C |
| Measurement |
Against distilled water |
| Sample/Reagent |
1: 20 |
| Reaction |
Kinetic test |
| Reaction Direction |
Increasing |
| Delay/lag/ time |
120 Secs |
| Interval time |
60 Secs |
| No: of Readings |
02 |
| Blank Absorbance limit |
<0.7 |
| Factor |
6592 |
| Low Normal at 37°C |
25 U/l |
| High Normal at 37°C |
192 U/l |
| Linearity |
1500 U/l |
MANUAL PROCEDURE
PIPETTE INTO TEST TUBE
Mix well, after 2 min , measure the change in absorbance. Read the
initial absorbance and start timer simultaneously
Read again after every 60 seconds for 2 minutes. Measure delta A/min.
CALCULATION AND LINEARITY
| delta A / min x 6592 = U/l CK |
The method is linear to a concentration of 1500 U/l. |