ORDER
INFORMATION
| Catalog No: |
Product Description: |
Pack Size: |
| TGL 50 |
TRIGLYCERIDE |
5 X 10 ML |
| TGL 100 |
TRIGLYCERIDE |
5 X 20 ML |
| TGL 200 |
TRIGLYCERIDE |
4 X 50 ML |
METHOD
Enzymatic colorimetric test
PRINCIPLE Triglycerides are determined after enzymatic hydrolysis
with lipases. The quinonemine indicator is formed from hydrogen peroxide,
4-aminophenazone, and 4-chlorophenol under the catalytic influence
of peroxidase.
SAMPLE
Serum. Heparinised plasma or EDTA plasma.
Stability
3 days at 2 - 8°C.
REAGENTS
Reagnet I : Enzyme regent
Reagent II : Buffer reagent
Reagent III : Triglyceride Standard : 200 mg/dl
REFERENCE VALUES
| Men |
60 - 165 mg/dl |
| Women |
40 - 140 mg/dl |
QUALITY CONTROL :
Accutestrol N - H
REFERENCES
Buccolo G., David M., Clin. Chem, 19 , (1973), 476
REAGENT PREPARATION
Dissolve the contents of one vial of enzyme reagent with the
volume of buffer reagent as specified on the enzyme vial.
|
STABILITY: The working reagent is stable for 120 days at 2-8°C.
store protected from sunlight.
AUTOMATED PARAMETERS
| Wave length |
520 nm |
| Reaction Type |
End Point |
| Cuvette |
1 cm light path |
| Reaction Temperature |
37°C |
| Measurement |
Against reagent blank |
| Sample/Reagent Ratio |
1: 100 |
| Incubation |
5 minutes |
| Maximum blank absorbance |
0.50 |
| Low Normal at 37°C |
40 mg/dl |
| High Normal at 37°C |
165 mg/dl |
| Linearity at 37°C |
1000 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 5 minutes at 37°C (or 15 mins at 20 - 25°C).
Measure absorbance of the sample (At) and standard (As) against reagent
blank. The colour is stable for 30 min at 20 - 25°C
CALCULATION AND LINEARITY
| AT
/ AS X conc. Std. = mg/dl Triglycerides |
The method is linear to a concentration of 1000 mg/dl. Dilute samples
above this concentration 1 : 1 with 0.9% saline and ressay. Multily
the result by 2. |