Take 400 microliter reagent R1 in ependroff cup.
Add 50 microliter sample to it.
Incubate at room temperature for 10 minutes.
Add 100 microliter R2 (Diazo A+Diazo B) after 10 minutes.
Take reading at 546nm.
Evaluate QC results. If QC results show major deviation from past, rerun batch.
If result comes more than 25mg/dl then dilute the sample about 1:1 with DI water and rerun the the sample.
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instructions for determining quantitative results when a result is not within the measurement interval: Dilution of sample with DI water is done in same way as done by Erba XL-640 automatically.
|Note:For setting the test sequence of TBIl and DBIL, it should always be kept in mind that these two parameters should always be kept before phosphorus and calcium in the “TEST SEQUENCE” format as it would minimize the inference of phosphate buffer from glucose reagent, which earlier had been interfering with phosphorus.|