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INFORMATION
| Catalog No: |
Product Description: |
Pack Size: |
| MB 10 |
CK-MB |
10 X 1.1 ML |
| MB 30 |
CK-MB |
10 X 3 ML |
METHOD
Kinetic method
PRINCIPLE
The procedure involves measurement of Creatinine kinase (CK) activity
in the presence of an antibody of CK-M monomer. This antibody completely
inhibits the activity of CK-MM and CK-BB. Than the CK method is used
to quantitatively determine CK-BB activity. CK catalyses the reaction
between creatinine Phosphate and ADP, giving creatinine and ATP. The
ATP & glucose are converted to ADP & Glucose-6-phosphate by
hexokinase. Glucose-6-phosphate dehydrogenase oxidises Glucose-6-phosphate
& reduces NAD to NADH. The rate of NADH formation is determined
photometrically at 340 nm & is directly proportional to CK-BB
activity. The CK-MB activity is obtained by multiplying the CK-BB
activity by two.
SAMPLE:
Serum free of hemolysis, heparinised plasma, protected from light.
Stability 24 hrs at 2-8°C; 3 days at -20°C
REFERENCE VALUES
| 0 - 24 U/l (37°C) |
| 0 - 14 U/l (30°C) |
QUALITY CONTROL :
Accutestrol N - H
REAGENTS COMPOSITION
Reagent I - Enzyme Reagent
Reagent II - Diluent
REFERENCES
Youngs et. al., Clin. Chem., 21 : 10 (1975)
REAGENT PREPARATION
Dissolve the contents of one vial of enzyme reagent with the volume
of diluent as specified on the enzyme vial, swirl to dissolve. |
STABILITY: 14 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 |
600 Secs |
| Interval time |
60 Secs |
| No: of Readings |
06 |
| Blank Absorbance limit |
<0.7 |
| Factor |
6752 |
| Low Normal at 37°C |
0 U/l |
| High Normal at 37°C |
24 U/l |
| Linearity |
1500 U/l |
MANUAL PROCEDURE
PIPETTE INTO TEST TUBE
Mix well, after 10 min , measure the change in absorbance.
Repeat readings every minute for next 6 minutes.
Calculate p A/min.
CALCULATION AND LINEARITY
p
A / min x 3376 = U/l CK-BB
CK-BB x 2 = U/l CK - MB |
The method is linear to a concentration of 1500 U/l. Samples above
1500 U/l should be dilute 1:1 with saline, re-assayed and the results
multiplied by two. |