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INFORMATION
| Catalog No: |
Product Description: |
Pack Size: |
| GOT 50 |
SGOT (AST)IFCC |
5 X 10 ML |
| GOT 100 |
SGOT (AST)IFCC |
5 X 20 ML |
| GOT 200 |
SGOT (AST)IFCC |
4 X 50 ML |
METHOD
Kinetic UV test
PRINCIPLE
Aspartate transaminase (GOT - AST) catalyses the reaction between
alpha - ketoglutaric acid and L-aspartate giving glutamate and oxaloacetate.
Oxaloacetate, in the presence of malate dehydrogenase (MDH) reacts
with NADH giving malate and NAD. The rate of NADH decrease is determined
photometrically and is directly proportional to the GOT activity in
the sample.
REAGENTS
Reagent I : Buffer Reagent
Reagent II : Enzyme reagent
SAMPLE:
Serum or plasma
REFERENCE VALUES
0 to 35 U/l at 37°C
QUALITY CONTROL
Accutestrol N - H
REAGENT PREPARATION
Dissolve one vial of enzyme reagent with amount of buffer reagent
as specified on the enzyme vial.
STABILITY
3 months at 2 - 8°C |
AUTOMATED PARAMETERS
| Wave length |
340 nm |
| Cuvette |
1 cm light path |
| Reaction Temperature |
37°C |
| Measurement |
Against distilled water |
| Reaction Type |
Kinetic test |
| Reaction Direction |
Decreasing |
| Sample/Reagent Ratio |
1 : 10 |
| Delay/Lag/time |
60 Secs |
| Interval time |
30 Secs |
| No: of Readings |
04 |
| Blank Absorbance limit |
>0.8 |
| Factor |
1746 |
| Low Normal at 37°C |
0 U/L |
| High Normal at 37°C |
35 U/L |
| Linearity at 37°C |
350 U/L |
MANUAL PROCEDURE
PIPETTE INTO TEST TUBE
| SAMPLE |
100 µl |
| REAGENT |
1000 µl |
Mix well and let stand for 1 min. at 37°C. Measure absorbance
decrease per minute during 3 minutes and determine the p
A/min
CALCULATION AND LINEARITY
| p
A/min. x 1746 = U/l AST |
The method is Linear upto 350 U/L
NOTES
Very low initial absorbance suggests very high activity of GOT;
dilute the samples appropriately and reassay. Multiply results with
dilution factor. Procedure & calculation will be the same.
REFERENCES
Expert Panel on enzyme of the IFCC, Clin. Chem. Acta, 70, PM, (1976),
Teitz., N.W.
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