ORDER
INFORMATION
| Catalog No: |
Product Description: |
Pack Size: |
| URI 50 |
URIC ACID |
5 x 10 ml |
| URI 100 |
URIC ACID |
5 X 20 ml |
| URI 200 |
URIC ACID |
4 x 50 ml |
METHOD
Enzymatic colorometric test
PRINCIPLE
Uric acid is converted by uricase to allantoin and hydrogen peroxide
which under the catalytic influence of peroxidase, oxidizes 3, 5 -
dichloro - 2 - hydroxybenzenesulfonic acid and 4-aminophenazone to
form a red-violet quinoneimine compound.
REAGENTS
Reagent I : Buffer
Reagent Reagent II : Enzyme reagent
Reagent Reagent III : Uric Acid standard : 5 mg/dl
SAMPLE
Serum, heparinised or EDTA plasma, urine.
Dilute urine 1 : 10 with distilled water.
Multiply the result by 10.
Stability : 5 days at 4 - 25°C.
REFERENCE VALUES
| Serum |
|
| Men |
3.4-7.0
mg/dl |
| Women |
2.4-5.7 mg/dl |
| Urine
|
250-750
mg/24h |
QUALITY CONTROL
Accutestrol N - H
REFERENCES
Caraway, W.T., Clin Chem.4, 239 (1963), Morin L.G., Clin Chem,
20, 51 (1974) Trivedi R.C., Rebar L., Berka E., Strong L., Clin. Chem.,
(1978) , 24 , 1908.
|
REAGENT PREPARATION
Dissolve contents of one vial of enzyme reagent with the volume of
buffer reagent as specified on the enzyme vial.
STABILITY : 60 days at 2 - 8°C /. (store protected from light)
AUTOMATED PARAMETERS
| Wave length |
340 nm |
| Cuvette |
1 cm light path |
| Reaction Temperature |
37°C |
| Measurement |
Against reagent blank |
| Reaction Type |
End Point |
| Reaction Direction |
Increasing |
| Sample/Reagent Ratio |
1: 40 |
| Incubation |
10 minutes |
| Maximum Blank Absorbance |
0.50 |
| Low Normal at 37°C |
2.4 mg/dl |
| High Normal at 37°C |
7.0 mg/dl |
| Linearity at 37°C |
20 mg/dl |
MANUAL PROCEDURE
PIPETTE INTO TEST TUBE
| |
BLANK |
STD |
SAMPLE |
| SAMPLE |
- |
- |
10 µl |
| STANDARD |
- |
10 µl |
- |
| REAGENT |
1000 µl |
1000 µl |
1000 µl |
Mix well, incubate for 10 mins at 37°C (or 15 mins at 20-25°C).
Measure absorbance of sample (Ac) and standard (As) against reagent
blank. The color is stable for 60 mins at 20-25°C.
CALCULATION AND LINEARITY
Ac/As x Conc of standard = mg/dl Uric Acid
This method is linear upto a concentration of 20 mg/dl.
Dilute samples above this concentration 1 : 1 with 0.9 % saline and
reassay. Multiply the result by 2. |