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. Author manuscript; available in PMC: 2009 Jan 31.
Published in final edited form as: J Immunol Methods. 2007 Dec 4;330(1-2):64–74. doi: 10.1016/j.jim.2007.10.020

Table 2.

Compensation matrix for a flow cytometry panel with nine fluorescence parametersa

Fluorochrome Detector
FL1 FL2 FL3 FL4 FL5 FL6 FL7 FL8 FL9
FITC 29 7.9 4.3 0.2 0 1.6 0 0
PE 0.8b 30.6 18.2 2.7 0 1.4 0 0
PE-TR/QD605 0.2/0 13/3.5c 82/1 17/0 0/0 0/0.4 1/0.1 0/0
PE-Cy5/PerCP 0/0 0.6/0 0.2/0 17.5/13.5 0/0 0/0 71/23.2 10.1/2.0
PE-Cy7 0 1.4 0.4 0.6 0 0 0 7.7
PacB 0 0 0 0 0 9.0 0 0
CasY 0 0 0 0 0 2.8 0 0
Alexa 647/APC 0/0 0/0 0/0 0.4/0.6 0/0 0/0 0/0 13.4/9.3
APC-Cy7 0 0 0 0.3 2.1 0 0 10.0
a

Compensation matrix generated in the FlowJo software.

b

A compensation particle set, consisting of uncoated polystyrene beads, or beads coated with anti-mouse Igκ (BD Biosciences), were stained with mAbs conjugated with each of the fluorochromes used.

c

Grey fields highlight where exchanging fluorochromes has the most significant effect on compensation needs.