Multiplex Assay Kit for Vimentin (VIM)

2. Add 100μL standard or sample to each well,
add 10μL magnetic beads, and incubate 90min at 37° C on shaker;
3. Remove liquid on magnetic frame, add 100μL prepared Detection Reagent A. Incubate 60min at 37° C on shaker;
4. Wash plate on magnetic frame for three times;
5. Add 100μL prepared Detection Reagent B, and incubate 30 min at 37° C on shaker;
6. Wash plate on magnetic frame for three times;
7. Add 100μL sheath solution, swirl for 2 minutes, read on the machine.
Inter-assay Precision (Precision between assays) : 3 samples with low, middle and high level of the target, etc. by FLIA (Flow Luminescence Immunoassay) were tested on 3 different plates, 8 replicates in each plate.
CV (%) = SD/meanX100, Intra-Assay: CV<10%, Inter-Assay: CV<12%
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
No significant cross-reactivity or interference between the target, etc. by FLIA (Flow Luminescence Immunoassay) and analogues was observed.
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