Bio-Rad Bio-Plex Pro™ Human Th17 Cytokine Assays - Manual (Page 35)

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Possible Solutions
Pipet carefully when adding standards, samples,
detection antibodies, and streptavidin-PE, especially
when using a multichannel pipet. Use a calibrated
pipet.Change pipet tip after every volume transfer.
If samples contain little or no analyte, negative
values observed may be due to statistical variation.
If assay drift is suspected, retest the samples
by positioning them next to the standards. If
contamination of standards is suspected, check
the standard replicate value and be careful when
adding samples to the wells. Matrix effects could
also produce negative sample values.
Bio-Plex Manager ™ software automatically
subtracts the Blank (B) FI value from all other
assay wells. While this has no impact on observed
concentrations of samples within the assay working
range, it may result in a negative FI value if the
Blank’s FI value is greater than either the standard
or sample value. If this is undesirable, then reformat
the blank wells as Sample (X) or Control (C), in the
protocol or results file.
Check if any interfering components such as
heparin-based anticoagulant, additives, or
gel from separators were introduced into the
samples. Avoid using hemolyzed and heavily
lipemic samples. Remove visible particulate in
samples by centrifugation. Avoid multiple freeze-
thaw cycles of samples.
Possible Causes
Poor Recovery
Improper pipetting
technique
Impact of Sample
Matrix
Negative MFI values in
samples or standards
Poor precision in
serum and
plasma sample
measurements